Skip to main content

BRIEF RESEARCH REPORT article

Front. Neurosci., 29 September 2021
Sec. Autonomic Neuroscience

Nitric Oxide Regulates Estrus Cycle Dependent Colonic Motility in Mice

  • 1Department of Physiology, The University of Melbourne, Parkville, VIC, Australia
  • 2School of Health and Biomedical Sciences, RMIT University, Bundoora, VIC, Australia
  • 3Faculty of Medicine, The University of Queensland, Herston, QLD, Australia

Women are more susceptible to functional bowel disorders than men and the severity of their symptoms such as diarrhea, constipation, abdominal pain and bloating changes over the menstrual cycle, suggesting a role for sex hormones in gastrointestinal function. Nitric oxide (NO) is a major inhibitory neurotransmitter in the gut and blockade of nitric oxide synthase (NOS; responsible for NO synthesis) increases colonic motility in male mice ex vivo. We assessed the effects of NOS inhibition on colonic motility in female mice using video imaging analysis of colonic motor complexes (CMCs). To understand interactions between NO and estrogen in the gut, we also quantified neuronal NOS and estrogen receptor alpha (ERα)-expressing myenteric neurons in estrus and proestrus female mice using immunofluorescence. Mice in estrus had fewer CMCs under control conditions (6 ± 1 per 15 min, n = 22) compared to proestrus (8 ± 1 per 15 min, n = 22, One-way ANOVA, p = 0.041). During proestrus, the NOS antagonist N-nitro-L-arginine (NOLA) increased CMC numbers compared to controls (189 ± 46%). In contrast, NOLA had no significant effect on CMC numbers during estrus. During estrus, we observed more NOS-expressing myenteric neurons (48 ± 2%) than during proestrus (39 ± 1%, n = 3, p = 0.035). Increased nuclear expression of ERα was observed in estrus which coincided with an altered motility response to NOLA in contrast with proestrus when ERα was largely cytoplasmic. In conclusion, we confirm a cyclic and sexually dimorphic effect of NOS activity in female mouse colon, which could be due to genomic effects of estrogens via ERα.

Introduction

Sexual dimorphism in gastrointestinal (GI) disorders is well documented and includes a higher prevalence of visceral pain disorders such as irritable bowel syndrome and gastroesophageal reflux disease as well as gallbladder and biliary tract diseases in women than in men of a similar age and health status (Palomba et al., 2011; Avramidou et al., 2018; Kim and Kim, 2018). Fluctuations in female hormone levels during the menstrual cycle, pregnancy, premenopausal, or menopausal states are associated with nausea, vomiting, abdominal pain, distension, abnormal satiety, bloating, diarrhea, or constipation (Hutson et al., 1989; Mayer et al., 1999). During pregnancy, constipation is increased and gastrointestinal motility is reduced (Tytgat et al., 2003; Bradley et al., 2007; Cullen and O’Donoghue, 2007; Boregowda and Shehata, 2013). However, the mechanisms underlying differential effects on GI motility in females are not well studied.

Rodents have a 4-day estrus cycle that includes fluctuations of sex hormones and are therefore a useful preclinical model for investigating influences of sex-hormones on GI function. The estrus cycle has four distinct stages, including proestrus, estrus, metestrus, and diestrus. During proestrus, which lasts for 18–24 h, plasma estrogen levels are high and fall drastically during the estrus phase resulting in ovulation. In contrast, primates (including human females) are in a 28-day menstrual cycle. Plasma estrogen levels reach a peak toward the end of the human follicular phase (comparable with the proestrus stage in rodents) and drop during ovulation which marks the start of the luteal phase (comparable with the estrus stage in rodents). During the diestrus phase, female rats have lower estrogen levels and slower gastric emptying than during estrous/proestrus (Chen et al., 1995). Estrogen also inhibits Cl secretion across the human and rat distal colon epithelium (O’Mahony et al., 2007; O’Mahony and Harvey, 2008). Estrogen dose-dependently inhibited the secretory responses induced by a well-established secretagogue cholera toxin in female rats, an effect seen in estrus but not in proestrus, but had no inhibitory effect on male rats (Alzamora et al., 2011a,b). Estrogen receptors are expressed on the cell membrane and in the nucleus both in mucosal epithelial cells and in enteric neurons of rodent gut (Campbell-Thompson et al., 2001; Li et al., 2016; Liu et al., 2019). Through these receptors, estrogen reportedly influences rodent gut physiology including secretion and motility (O’Mahony et al., 2007; Alzamora et al., 2011a; Li et al., 2016; Liu et al., 2019). For example, gastric emptying is significantly delayed in pregnant female rats (Shah et al., 2000, 2001). In addition, administration of the circulating form of estrogen, estradiol (alone or together with progesterone) reduced gastric emptying in adult female rats (Chen et al., 1995). A recent study, indeed, suggests that estrogen, not progesterone, is responsible for reducing rapid gastric emptying and restoring gastric nitrergic relaxation in ovariectomized mice fed with a high fat diet (Sprouse et al., 2020).

In women, estrogen concentrations are reported to correlate with the menstrual cycle dependent changes in amplitude and velocity of the jejunal migrating motor complex (Aytuğ et al., 2001). Moreover, several lines of evidence suggest that changes in rodent gut function during the estrus cycle are primarily due to fluctuations in estrogen rather than progesterone. Colonic transit is slower during the proestrus-estrus phases and faster during the metestrus-diestrus phases in female rats (Chen et al., 1995). In the absence of the estrus cycle (i.e., in ovariectomized female rats), colonic transit is faster in keeping with a metestrus-diestrus phenotype typical of low estrogen levels (Ryan and Bhojwani, 1986). The literature also suggests that the A-type potassium currents that regulate neuronal excitability are suppressed by estrogen and could be linked to altered colonic motility associated with menstrual cycle, pregnancy, and menopause (Beckett et al., 2006). Furthermore, estrogens modulate colonic function in mice via G protein-coupled estrogen receptors (GPER) expressed in gut neurons (Li et al., 2016) and ileal contractility via actions on GPER and the estrogen receptors alpha (ERα) and beta (ERβ), both of which are expressed in enteric neurons (Liu et al., 2019).

The enteric neural circuitry regulating colonic motility contains sensory neurons, interneurons and (excitatory and inhibitory) motor neurons. These neurons use different neurotransmitters including acetylcholine (ACh), vasoactive intestinal peptide (VIP), serotonin (5-HT), and the main inhibitory neurotransmitter in the colon; nitric oxide (NO; Furness, 2006). Neuronal nitric oxide synthase (nNOS) catalyzes the de novo synthesis of NO and is expressed by both inhibitory motor neurons that innervate the circular muscle layer of the mouse colon (Sang and Young, 1996; Spencer et al., 1998) and some myenteric interneurons (Sang and Young, 1996). Colonic contraction complexes include motility patterns that are neurally regulated, rhythmic and spontaneously occurring known as colonic motor complexes or CMCs (Spencer, 2001; Corsetti et al., 2019).

Estrogen potentiates NOS activity in the brain and in the enteric nervous system (ENS; Weiner et al., 1994; Figueroa and Massmann, 1995; Kleinert et al., 1998; McNeill et al., 2002). Interactions between NO activity and the estrus cycle in rodent brain tissue are well documented (Collado et al., 2003; Carrillo et al., 2007; Sica et al., 2009). In the GI tract, estrogens enhance nNOS protein expression in myenteric neurons of the gastric fundus and the colon of estrogen-treated ovariectomized female rats (Shah et al., 2000, 2001). Chronic estrogen deficiency (in follicle stimulating hormone receptor knock-out female mice) decreases nNOS activity leading to reduced nitrergic relaxation in the gastric antrum and also contributes to reduced motility observed in gastroparesis (Ravella et al., 2013). It remains unclear, however, whether changes in estrogen levels affect colonic activity via the inhibitory neurotransmitter, NO. In this study we therefore investigated the role of NO in cyclic differences using ex vivo colonic motility and immunofluorescence assays during low (estrus) and high (proestrus) estrogen phases in female mice.

Materials and Methods

Animal Tissue

Eight to twelve-week-old female mice in estrus and proestrus were selected by scanning vaginal smears (Tran et al., 2012; Cora et al., 2015; Balasuriya et al., 2016). Briefly, vaginal content was gently flushed into a blunted sterile Pasteur pipette containing 30–50 μl of distilled water and contents were air dried on a microscope slide and stained using a Shandon Wright-Giemsa Stain Kit (Thermo Fisher Scientific, Australia). Slides were scanned with a light microscope (AxioCam, Carl Zeiss Pty., Ltd., North Ryde, NSW, Australia) and proestrus and estrus were identified by their specific cytological profiles. As per (Balasuriya et al., 2016), proestrus cytology consisted of large numbers of nucleated epithelial cells whereas cells from estrus stage vaginal smears were cornified, non-nucleated epithelial cells. Female mice were maintained under a 12 h/12 h light-dark cycle from 0600 to 1800 h. Vaginal smears were taken between 0800 and 0900 h. Animals were culled by cervical dislocation around 1000 h, as approved by the University of Melbourne Animal Experimentation Ethics Committee (approval no: 1011897) and according to guidelines of the National Health and Medical Research Council of Australia. The whole colon was dissected and placed in an organ bath superfused with warmed (36°C) physiological saline solution (composition, mM: NaCl 118, KCl 4.6, NaH2PO4 1, NaHCO3 25, MgSO4 1.2, D-glucose 11, CaCl2 2.5; bubbled with 95% O2–5% CO2). The oral end of the colon tissue was cannulated to an inlet connected to a reservoir of physiological saline, and the anal end to an outflow tube that provided a back-pressure of 3–4 cm H2O (Gwynne et al., 2004; Roberts et al., 2007; Swaminathan et al., 2016).

Video Imaging

Video imaging analysis of colonic motility was conducted as previously described (Balasuriya et al., 2016; Swaminathan et al., 2016) using female mice during estrus and proestrus. Briefly, colonic motility was recorded ex vivo using a Logitech camera (QuickCam Pro 4000; I-Tech, Ultimo, NSW, Australia) mounted directly above the organ bath. In-house software (Scribble 2.0) and a purpose-built (Matlab, 2014) plugin, Analyse 2.0, were used to convert recorded video segments (15 min duration) to spatiotemporal maps where the diameter of the colon is mapped [as a spatiotemporal (ST) map] along the length of the segment as a function of time (x axis: time, y axis: colon length). Blue–green pixels on ST maps indicate relaxed tissue and yellow–red pixels identify constricted regions (Figure 1). Under the experimental conditions of 2–4 cm H2O pressure migrating motor complexes originating at the oral end and propagating to anal direction were observed in the colon preparations. The frequency of propagating contractions previously described as colonic migrating motor complexes (CMMCs) was manually counted from the ST maps (Balasuriya et al., 2016). Resting colonic diameter measures were obtained using in built functions of the software as previously reported (Gwynne et al., 2004; Balasuriya et al., 2016).

FIGURE 1
www.frontiersin.org

Figure 1. (A) Spatiotemporal maps showing the number of CMCs during 15 min recordings of estrus and proestrus colon under the control conditions and on exposure to NOLA (100 μM). (B) Females in estrus had fewer CMCs compared to proestrus (n = 23, unpaired t-test, p = 0.042). (C) Resting colonic diameters were similar between the groups under control conditions. (D) Proestrus colons showed a larger percentage increase in the number of CMCs on exposure to NOLA compared to colons from mice during estrus (n = 10, unpaired t-test, p = 0.003). (E) NOLA similarly decreased resting gut diameter in both estrus and proestrus groups (n = 10, unpaired t-test, p = 0.97). Horizontal scale bar = 60 s, vertical scale bar = 0.5 cm. **p < 0.01 and *p < 0.05.

Motility experiments began with a 30 min equilibration period, followed by four 15 min control video recordings (1 h control period). The effects of NOS inhibition were studied by adding the NOS antagonist Nitro-L-arginine (NOLA; 100 μM, Sigma-Aldrich, St. Louis, MO, United States, Middlesex, United Kingdom) to the bath. Motility was recorded for another 1 h (i.e., in the form of four 15 min video files). A 1 h washout period during which the drug solution was replaced with physiological saline was subsequently conducted.

Immunohistochemistry

Tissue Preparation

The immunofluorescence method used in this study was as previously reported (Neal and Bornstein, 2007; Roberts et al., 2007) with minor adaptations. Briefly, colons were dissected from the culled mice (males, females during estrus, and proestrus) and placed in a petri dish lined with a silicon elastomer (Sylgard 184, Dow Corning, United States) containing phosphate buffered saline (0.1 M PBS, pH 7.2, filtered three times). The colon was cut open along the mesenteric boarder and stretched and pinned flat (mucosal side facing up) onto the petri dish using insect pins (supplier, Sydney, NSW, Australia). Tissue preparations were fixed in 4% formaldehyde overnight at 4°C. The fixative was then washed (three 10 min washes in 0.1 M PBS). Using fine dissecting instruments, the mucosa, submucosal plexus and circular muscle layers were carefully peeled away from the distal colon to expose the myenteric neurons with an underlying longitudinal muscle layer (LMMP). This whole mount preparation was used for immunofluorescence. A small number of circular muscle cells remained following peeling of the mucosa and SMP layers to reveal myenteric ganglia.

Immunofluorescence

Whole mount preparations of myenteric plexus were permeabilized and blocked using 0.01% triton (ProSciTech, Thuringowa Central, QLD, Australia) in 10% CAS block (Invitrogen Australia Pty., Ltd., Mount Waverley, VIC, Australia) for 30 min at room temperature and incubated overnight with primary antisera (Table 1) at 4°C. The next day, tissue samples were washed three times at 10 min intervals using filtered 0.1 M PBS and incubated with fluorescence tagged secondary antisera (Table 1) for 2.5 h at room temperature. Preparations were then washed with filtered PBS and mounted on slides using fluorescence mounting medium (Dako Australia Pty., Ltd., Botany, NSW, Australia) and secured with a glass coverslip. Images were captured using a confocal microscope (Zeiss LSM510 fluorescence microscope; Zeiss, Gladesville, NSW, Australia) and Zeiss LSM software, (version 4.2.0.121).

TABLE 1
www.frontiersin.org

Table 1. Antisera used for evaluation of NOS neurons and estrogen receptor alpha (ERα) in whole mount preparations of myenteric plexus.

Neurons were considered to be part of a separate ganglion if they were separated from the edge of the nearest neuron by at least two cell body widths as described by Baudry et al. (2012). Using that definition as a guide, six randomly selected ganglia from each region of the colon were counted. The neuronal marker Hu (anti-ANNA-1, 1:10000 dilution, a gift from Dr. Lennon, United States) was used to label all the neurons of the preparation (Hotta et al., 2013; Fung et al., 2014). The number of Hu positive cells corresponded to the total number of neurons in counted ganglia. Numbers of ERα and ERβ positive cells per ganglion as well as the expression in the nucleus were manually counted using ImageJ software and its Cell counter plugin (NIH, Bethesda, MD, United States) and the percentage was calculated.

Statistical Analyses

Data were analyzed by one-way ANOVA or Student’s t test as appropriate. n is the number of animals from which measures were taken, and statistical significance was set at P < 0.05. Data are presented as mean ± standard error of the mean (SEM).

Results

Reduced Number of CMCs During Estrus Compared to Proestrus

To assess differences in GI motility between estrus and proestrus, we examined CMC parameters in female mice under control conditions. An advantage of using the ex vivo organ bath approach is that it enables large intestinal motility to be studied without the influence of the central nervous system. Mice in estrus exhibited fewer CMCs compared to proestrus (estrus: 6 ± 1 CMCs per 15 min, n = 23; proestrus: 8 ± 1 CMMCs/15 min, n = 23; p = 0.041, Figures 1A,B). However, resting colonic diameter was unchanged between estrus and proestrus (3.9 ± 0.14 mm and 3.7 ± 0.21 mm, respectively, n = 17 in each group; p = 0.326, Figure 1C).

NOLA Exerts an Estrus Cycle Dependent Effect on CMC Frequency

It is well established that CMC frequency is increased in the presence of the NOS inhibitor, NOLA, in male mouse colon (Spencer et al., 1998; Spencer, 2001). When responses of estrus and proestrus colons to NOLA were compared (Figure 1D), proestrus colon preparations had a greater percentage increase in CMC numbers (189 ± 46%) than estrus colons (15 ± 14%, p = 0.0028, n = 10 in each group). Control values were 7 ± 1 and 5 ± 1 CMCs/15 min for estrus and proestrus, respectively, and 7 ± 1 and 9 ± 1 CMCs/15 min for estrus and proestrus, respectively, under NOLA exposure (n = 10).

In the same preparations, NOLA significantly reduced the resting colonic diameter in estrus and proestrus compared to control conditions (estrus: NOLA 2.7 ± 0.1 mm, control 3.5 ± 0.03 mm, p = 0.01; proestrus: NOLA 2.7 ± 0.1 mm, control 3.2 ± 0.1 mm, p = 0.001). But the percentage decrease in resting colonic diameter between estrus and proestrus colons in response to NOLA was unchanged (23 ± 3% and 22 ± 3%, respectively, p = 0.97, Figure 1E). Contraction velocity and the distance over which contractions propagate were also unchanged.

Increased Numbers of NOS Immunoreactive Myenteric Neurons in Estrus

A greater proportion of myenteric neurons were immunoreactive for nNOS in distal colons from mice in estrus compared with proestrus. During estrus, 48 ± 2% of the total number of myenteric neurons per ganglion were immunoreactive for nNOS (215 of 457 Hu-positive myenteric neurons expressed NOS; n = 3 animals, Figure 2A). During proestrus, 39 ± 1% of myenteric neurons expressed nNOS (160 neurons of a total of 414 Hu-positive myenteric neurons expressed NOS; n = 3 animals; p = 0.042, Figure 2A). nNOS labeling was also observed in myenteric varicosities and in varicosities adjacent to residual smooth muscle cells present in the myenteric plexus preparations.

FIGURE 2
www.frontiersin.org

Figure 2. (A) Immunofluorescence histochemical double-staining of the whole-mount preparations of the mouse colon. Estrus myenteric neurons had a significantly greater number of NOS expressing neurons compared to proestrus myenteric plexus (estrus 48 ± 2% and proestrus 39 ± 1%, n = 3, p = 042 one-way ANOVA). The pan neuronal marker Hu is shown in red and NOS expressing myenteric neurons in green. Scale bar = 20 μm. (B) Co-labeling of NOS neurons with estrogen receptor alpha in a randomly selected female mouse. Whole mounts of myenteric ganglia showing co-labeling of Hu (red), NOS (green), and ERα (magenta). ERα is expressed in the majority of nuclei of myenteric neurons (closed arrows). Arrowheads indicate myenteric neurons co-labeled with NOS and ERα. Scale bar = 30 μm. *p < 0.05.

Prominent Nuclear Expression of ERα During Estrus

To investigate how motility might be altered with changes in estrogen concentrations during the estrus cycle, we used immunohistochemistry to localize estrogen receptors in myenteric plexus in male and female mice. The ERα antibody was first tested in cross sections of uterine tissue and clear labeling of ERα was observed in the glandular epithelial cells (Figure 3C). Labeling for estrogen receptors in female mice in estrus (n = 3) and proestrus (n = 3) periods was conducted. ERα labeling was observed in 87 ± 2% and 90 ± 3% of Hu positive myenteric neurons in males and females, respectively (Figure 3A). ERα was strongly labeled in neuronal cell bodies, but some labeling was also present in neuronal processes. In some preparations, low levels of ERα labeling were observed in residual circular muscle as reported previously (Beckett et al., 2006). During estrus, ERα is predominantly localized within the nucleus. In contrast, during proestrus ERα labeling was observed in the cytoplasm of most neurons, with few neurons showing a nuclear localization. The distribution of ERα in males was more uniform with labeling in both the nuclei and cytoplasm of most neurons in the myenteric plexus. During estrus, the proportion of neurons labeling for Hu together with ERα in the nucleus was greater compared to both proestrus females and males (87 ± 2.03, 42 ± 1.51, and 61 ± 1.44, respectively, p < 0.001, Figure 3A).

FIGURE 3
www.frontiersin.org

Figure 3. Whole mount preparations of myenteric plexus expressing pan neuronal marker Hu in red and ERα/ERβ in green. Significantly higher numbers of myenteric neurons expressed ERα in the nucleus during estrus while having some cytoplasmic expression compared to proestrus females and male myenteric neurons expressing less nuclear and cytoplasmic ERα. ERβ expression was more cytoplasmic in all tissue samples and showed no significant difference in expression between groups. Scale bar = 20 μm (n = 3, One-way ANOVA, ***p < 0.001). (A) Localization of ERα in the myenteric plexus preparations of estrus, proestrus, and male colon: ERα labeling was observed in more than 90% of myenteric neurons in both male and female mice. Images of representative myenteric ganglia, demonstrating neurons stained for Hu, ERα, and merged images of both Hu and ERα. During estrus stage, ERα labeling is predominantly nuclear while during proestrus and in male mice both nuclear and cytoplasmic labeling was observed (arrows indicate nuclear labeling of ERα). Scale bars = 20 μm. Graph shows quantified data (n = 3) where there was significantly higher nuclear localization observed during estrus stage compared to both proestrus and male preparations (***p < 0.001). (B) Localization of ERβ in the myenteric plexus preparations of estrus, proestrus, and male colon: localization of the estrogen receptor beta (ERβ) is unchanged during estrus. ERβ labeling was observed in more than 90% of myenteric neurons in both male and female mice. Images of representative myenteric ganglia, demonstrating neurons stained for Hu, ERα, and merged images of Hu and ERα. No significant difference was observed among the groups with respect to nuclear labeling of ERβ (arrows indicate nuclear labeling of ERβ). Scale bars = 20 μm. The graph shows quantified data (n = 3) where there was no significant difference among the groups (p > 0.05). (C) Specificity of ERα PA1-308-antiserum was tested in a uterine tissue. Labeling was observed in the glandular epithelial cells of the uterus (frozen cross section). Scale bar = 20 μm.

Using the approach described above, we quantified the subcellular localization of the ERβ antiserum (obtained from Prof. John Hutson, Surgical Research Group, Infection and Immunity, Murdoch Children’s Research Institute, Parkville, VIC, Australia; Nation et al., 2011) in mouse myenteric plexus in the colon. In contrast with the findings for ERα, we found no differences in the nuclear localization of ERβ in the myenteric plexus between estrus or proestrus stages or in males (20 ± 3, 27 ± 6, and 23 ± 3, respectively, Figure 3B).

We observed ERα expression in all NOS immunoreactive myenteric neurons as well as in nearly all nNOS-negative neurons (Figure 2B). Thus, the biological machinery required for estrogen to exert a transcriptional effect on neurons regulating colonic motility is present in mouse myenteric neurons.

Discussion

In this study we showed that altered colonic motility during the estrus cycle correlates with fluctuating levels of sex steroid hormones in female C57Bl/6 mice. Estrogen levels regulate the synthesis of NO (Weiner et al., 1994; Grohe et al., 2004; Upmacis et al., 2011), a potent inhibitory neurotransmitter in the gut affecting motility (Spencer et al., 1998; Spencer, 2001; Powell and Bywater, 2001). During estrus, when plasma estrogen concentrations are low, there were fewer CMCs compared to proestrus when plasma concentrations are high. It is well established that many functional effects of estrogens on gene expression are elicited within the cell nuclei (Serova et al., 2006). Although plasma estrogen concentrations are higher during proestrus, the genomic effects of estrogens that influence secretion in the GI tract of rodents do not occur until estrus (Alzamora et al., 2011a,b). This delay in effect could be due to the time taken for translocation of estrogen-estrogen receptor complexes to cell nuclei and the time course of protein synthesis.

We found ERα expression in almost all Hu positive, and particularly in all nNOS immunoreactive, myenteric neurons. Changes in localization and function of estrogen receptors are observed with altered neuronal functioning in both the CNS (McEwen and Alves, 1999; Maggi et al., 2004; Hedges et al., 2012) and the ENS (Campbell-Thompson et al., 2001; Shah et al., 2001; Kawano et al., 2004; Cote et al., 2015). Here, we observed increased nuclear localization of ERα, but not ERβ, during estrus in myenteric neurons in the mouse colon. Nuclear ERα localization results from cytoplasmic receptors being translocated to the nucleus to trigger transcriptional effects via estrogen response elements. The observed increase in nuclear expression of ERα in myenteric neurons during estrus correlates with increased nNOS expression in myenteric neurons and changes in colonic motility. More myenteric neurons were immunoreactive for NOS during estrus compared to proestrus in the mouse distal colon. The percentage of NOS immunoreactive neurons observed during estrus (48 ± 2%) is also greater than that reported for male C57Bl/6 mice [41.7%; (Gamage et al., 2013)] and for male colons of other mouse strains such as Balb/c [approximately 35%; Balb/c (Sang and Young, 1996)].

It is well established that pharmacological blockade of NOS increases CMC frequency (Fida et al., 1997; Powell and Bywater, 2001) suggesting that NO levels in the myenteric plexus exert an inhibitory brake on the CMC pattern generator. Blockade of NOS with NOLA significantly increased the number of CMCs in proestrus female mice but had no effect in estrus females. However, this treatment significantly reduced the resting colonic diameter in both groups suggesting that levels of nNOS in inhibitory motor neurons are not cycle-dependent. An alternative explanation is that there are cycle-dependent changes in nNOS levels in interneurons, which also influence colonic constriction. CMC frequency increases and the corresponding interval between CMCs reduces in response to NOS inhibition in male mice (Lyster et al., 1995; Fida et al., 1997; Powell et al., 2003; Roberts et al., 2007). These findings suggest that during proestrus, where plasma estrogen levels are high but actual genomic effects of estrogens are low, female mice present a similar phenotype to male mice where estrogen levels/effects are generally low. However, during the estrus phase, where functional effects of estrogens are higher, NOS blockade did not eliminate relaxation of colonic smooth muscles. The expression of NOS in a new population of interneurons with unknown connectivity could produce mutually compensating changes in the motor pattern generator leading to no net effect of inhibition of NO synthesis during estrus. This indicates a direction for further experimentation. In contrast, during proestrus, neural NOS levels within the ganglia are low enough that reduced synthesis can disinhibit the pattern generator. It is important to note that NO can suppress synaptic transmission in the ENS (Tamura et al., 1993; Yuan et al., 1995) and NO in fact mediates inhibitory post synaptic potentials (IPSPs) in guinea-pig colon (Dickson et al., 2007).

These data suggest that there is a sexually dimorphic and estrus cycle-dependent change in nNOS expression in myenteric neurons and NO-mediated colonic motility. We show that this effect correlates with the nuclear expression of ERα. Therefore, estrogens are probably responsible for the changes observed. However, it is important to understand the mechanisms that could be responsible for increased numbers of nNOS neurons during estrus, as this occurs in a relatively short time window of only 18–24 h between proestrus and estrus. Further clarification of changes in enteric neuronal proportions should be carried out for a number of additional neurochemical markers and with larger animal numbers in a future study to better characterize changes in enteric neuronal properties in mice during the estrus cycle.

Our findings using an ex vivo organ bath approach suggest involvement of nuclear ERα in modulating colonic motility. This method is advantageous in that the gastrointestinal structure remains relatively intact, enabling analysis of the propagating motor complexes under close to physiological conditions. A previous study by Li et al. (2016) using muscle strip preparations reported that estrogens acting on the GPER membrane estrogen receptor are responsible for cyclic changes in gut smooth muscle contraction. This group also showed that application of G1, the selective GPER agonist, increased nNOS protein expression in mouse LMMP preparations (Li et al., 2016). In contrast with our approach, this study did not assess the relative contributions of the nuclear and membrane estrogen receptors in modulating colonic motility. In their experiments, blockade of GPER only partially recovered estrogen-mediated smooth muscle contractions in muscle strips, suggesting that estrogen also triggers contractions via other pathways such as by activation of nuclear estrogen receptors. The study by Li et al. (2016) therefore does not fully support an exclusive role of GPER in modulating estrogen-mediated colonic motility and is compatible with the current findings suggesting that nuclear ERα plays a role in estrogen modulation of colonic motility.

Possible Mechanisms by Which Estrogen Affects NO

Estrogens can affect gene regulation and posttranscriptional modifications of NOS protein (Grohe et al., 2004; Showkat Ali et al., 2012). Proper functioning of the NOS enzyme depends on several factors including the availability of cofactors and post-translational modifications (Michel and Vanhoutte, 2010). Estrogen elevates the expression of BH4, a cofactor binding to NOS which is an important limiting step in NO biosynthesis (Klatt et al., 1993; Vasquez-Vivar et al., 1999; Lam et al., 2006; Serova et al., 2006). In vivo experiments conducted with female diabetic rats confirmed that a diabetes-induced delay in gastric emptying can be restored by supplementation of BH4 through restoring nNOS activity and NO synthesis (Gangula et al., 2010). Importantly, it has been reported that there are estrogen response elements in the promotor region of the nNOS gene (Chiueh et al., 2003). Therefore, estrogen can modulate NO functioning through directly affecting nNOS gene regulation or via cofactors required for NO biosynthesis, further illustrating the importance of this pathway in the gastrointestinal tract.

In summary, estrogen receptors are expressed in the vast majority of myenteric neurons and increased nuclear expression of ERα was observed alongside an increase in nNOS numbers during estrus in mice. Here we propose that cyclic changes in propagating colonic motility in mice are due to a change in nNOS activity due to genomic effects of estrogen acting on ERα.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The animal study was reviewed and approved by the University of Melbourne Animal Experimentation Ethics Committee.

Author Contributions

GB and SN performed the experiments. JB and GB conceived and designed the experiments. GB, EH-Y, and JB wrote the manuscript. All authors have approved the final version of the manuscript and agreed to be accountable for all aspects of the work.

Funding

This study was supported by the NHMRC grant 1006453 (JB) and an NHMRC grant to EH-Y (APP2003848).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Alzamora, R., O’Mahony, F., Bustos, V., Rapetti-Mauss, R., Urbach, V., Cid, L., et al. (2011a). Sexual dimorphism and oestrogen regulation of KCNE3 expression modulates the functional properties of KCNQ1 K channels. J. Physiol. 589, 5091–5107. doi: 10.1113/jphysiol.2011.215772

PubMed Abstract | CrossRef Full Text | Google Scholar

Alzamora, R., O’Mahony, F., and Harvey, B. J. (2011b). Estrogen inhibits chloride secretion caused by cholera and Escherichia coli enterotoxins in female rat distal colon. Steroids 76, 867–876.

Google Scholar

Avramidou, M., Angst, F., Angst, J., Aeschlimann, A., Rössler, W., and Schnyder, U. (2018). Epidemiology of gastrointestinal symptoms in young and middle-aged Swiss adults: prevalences and comorbidities in a longitudinal population cohort over 28 years. BMC Gastroenterol. 18:21. doi: 10.1186/s12876-018-0749-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Aytuğ, N., Giral, A., Imeryüz, N., Enç, F. Y., Bekiroğlu, N., Aktaş, G., et al. (2001). Gender influence on jejunal migrating motor complex. Am. J. Physiol. Gastrointest. Liver Physiol. 280, G255–G263.

Google Scholar

Balasuriya, G. K., Hill-Yardin, E. L., Gershon, M. D., and Bornstein, J. C. (2016). A sexually dimorphic effect of cholera toxin: rapid changes in colonic motility mediated via a 5-HT3 receptor-dependent pathway in female C57Bl/6 mice. J. Physiol. 594, 4325–4338. doi: 10.1113/jp272071

PubMed Abstract | CrossRef Full Text | Google Scholar

Baudry, C., Reichardt, F., Marchix, J., Bado, A., Schemann, M., des Varannes, S. B., et al. (2012). Diet-induced obesity has neuroprotective effects in murine gastric enteric nervous system: involvement of leptin and glial cell line-derived neurotrophic factor. J. Physiol. 590, 533–544.

Google Scholar

Beckett, E. A. H., McCloskey, C., O’Kane, N., Sanders, K. M., and Koh, S. D. (2006). Effects of female steroid hormones on A-type K+ currents in murine colon. J. Physiol. 573, 453–468. doi: 10.1113/jphysiol.2006.107375

PubMed Abstract | CrossRef Full Text | Google Scholar

Boregowda, G., and Shehata, H. A. (2013). Gastrointestinal and liver disease in pregnancy. Best Pract. Res. Clin. Obstet. Gynaecol. 27, 835–853.

Google Scholar

Bradley, C. S., Kennedy, C. M., Turcea, A. M., Rao, S. S., and Nygaard, I. E. (2007). Constipation in pregnancy: prevalence, symptoms, and risk factors. Obstet. Gynecol. 110, 1351–1357. doi: 10.1097/01.aog.0000295723.94624.b1

CrossRef Full Text | Google Scholar

Campbell-Thompson, M., Reyher, K. K., and Wilkinson, L. B. (2001). Immunolocalization of estrogen receptor alpha and beta in gastric epithelium and enteric neurons. J. Endocrinol. 171, 65–73. doi: 10.1677/joe.0.1710065

PubMed Abstract | CrossRef Full Text | Google Scholar

Carrillo, B., Pinos, H., Guillamon, A., Panzica, G., and Collado, P. (2007). Morphometrical and neurochemical changes in the anteroventral subdivision of the rat medial amygdala during estrous cycle. Brain Res. 1150, 83–93. doi: 10.1016/j.brainres.2007.02.073

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, T. S., Doong, M. L., Chang, F. Y., Lee, S. D., and Wang, P. S. (1995). Effects of sex steroid hormones on gastric emptying and gastrointestinal transit in rats. Am. J. Physiol. 268, G171–G176.

Google Scholar

Chiueh, C., Lee, S., Andoh, T., and Murphy, D. (2003). Induction of antioxidative and antiapoptotic thioredoxin supports neuroprotective hypothesis of estrogen. Endocrine 21, 27–31. doi: 10.1385/endo:21:1:27

CrossRef Full Text | Google Scholar

Collado, P., Guillamon, A., Pinos, H., Perez-Izquierdo, M. A., Garcia-Falgueras, A., Carrillo, B., et al. (2003). NADPH-diaphorase activity increases during estrous phase in the bed nucleus of the accessory olfactory tract in the female rat. Brain Res. 983, 223–229. doi: 10.1016/s0006-8993(03)02973-1

CrossRef Full Text | Google Scholar

Cora, M. C., Kooistra, L., and Travlos, G. (2015). Vaginal cytology of the laboratory rat and mouse: review and criteria for the staging of the estrous cycle using stained vaginal smears. Toxicol. Pathol. 43, 776–793. doi: 10.1177/0192623315570339

PubMed Abstract | CrossRef Full Text | Google Scholar

Corsetti, M., Costa, M., Bassotti, G., Bharucha, A. E., Borrelli, O., Dinning, P., et al. (2019). First translational consensus on terminology and definitions of colonic motility in animals and humans studied by manometric and other techniques. Nat. Rev. Gastroenterol. Hepatol. 16, 559–579. doi: 10.1038/s41575-019-0167-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Cote, M., Bourque, M., Poirier, A. A., Aube, B., Morissette, M., Di Paolo, T., et al. (2015). GPER1-mediated immunomodulation and neuroprotection in the myenteric plexus of a mouse model of Parkinson’s disease. Neurobiol. Dis. 82, 99–113. doi: 10.1016/j.nbd.2015.05.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Cullen, G., and O’Donoghue, D. (2007). Constipation and pregnancy. Best Pract. Res. Clin. Gastroenterol. 21, 807–818.

Google Scholar

Dickson, E. J., Spencer, N. J., Hennig, G. W., Bayguinov, P. O., Ren, J., Heredia, D. J., et al. (2007). An enteric occult reflex underlies accommodation and slow transit in distal large intestine. Gastroenterolo 132, 1912–2410.

Google Scholar

Fida, R., Lyster, D. J., Bywater, R. A., and Taylor, G. S. (1997). Colonic migrating motor complexes (CMMCs) in the isolated mouse colon. Neurogastroenterol. Motil. 9, 99–107. doi: 10.1046/j.1365-2982.1997.d01-25.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Figueroa, J. P., and Massmann, G. A. (1995). Estrogen increases nitric oxide synthase activity in the uterus of nonpregnant sheep. Am. J. Obstet. Gynecol. 173, 1539–1545. doi: 10.1016/0002-9378(95)90646-0

CrossRef Full Text | Google Scholar

Furness, J. B. (2006). The Enteric Nervous System. Hoboken, NJ: Blackwell Publishing.

Google Scholar

Fung, C., Unterweger, P., Parry, L. J., Bornstein, J. C., and Foong, J. P. (2014). VPAC1 receptors regulate intestinal secretion and muscle contractility by activating cholinergic neurons in guinea pig jejunum. Am. J. Physiol. Gastrointest. Liver Physiol. 306, G748–G758.

Google Scholar

Gamage, P. P., Ranson, R. N., Patel, B. A., Yeoman, M. S., and Saffrey, M. J. (2013). Myenteric neuron numbers are maintained in aging mouse distal colon. Neurogastroenterol. Motil. 25, e495–e505.

Google Scholar

Gangula, P. R., Mukhopadhyay, S., Ravella, K., Cai, S., Channon, K. M., Garfield, R. E., et al. (2010). Tetrahydrobiopterin (BH4), a cofactor for nNOS, restores gastric emptying and nNOS expression in female diabetic rats. Am. J. Physiol. Gastroint. Liver Physiol. 298, G692–G699.

Google Scholar

Grohe, C., Kann, S., Fink, L., Djoufack, P. C., Paehr, M., van Eickels, M., et al. (2004). 17 Beta-estradiol regulates nNOS and eNOS activity in the hippocampus. Neuroreport 15, 89–93. doi: 10.1097/00001756-200401190-00018

PubMed Abstract | CrossRef Full Text | Google Scholar

Gwynne, R. M., Thomas, E. A., Goh, S. M., Sjovall, H., and Bornstein, J. C. (2004). Segmentation induced by intraluminal fatty acid in isolated guinea-pig duodenum and jejunum. J. Physiol. 556:557. doi: 10.1113/jphysiol.2003.057182

PubMed Abstract | CrossRef Full Text | Google Scholar

Hedges, V. L., Ebner, T. J., Meisel, R. L., and Mermelstein, P. G. (2012). The cerebellum as a target for estrogen action. Front. Neuroendocrinol. 33:403–411. doi: 10.1016/j.yfrne.2012.08.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Hotta, R., Stamp, L. A., Foong, J. P., McConnell, S. N., Bergner, A. J., Anderson, R. B., et al. (2013). Transplanted progenitors generate functional enteric neurons in the postnatal colon. J. Clin. Investigat. 123, 1182–1191.

Google Scholar

Hutson, W. R., Roehrkasse, R. L., and Wald, A. (1989). Influence of gender and menopause on gastric emptying and motility. Gastroenterology 96, 11–17. doi: 10.1016/0016-5085(89)90758-0

CrossRef Full Text | Google Scholar

Kawano, N., Koji, T., Hishikawa, Y., Murase, K., Murata, I., and Kohno, S. (2004). Identification and localization of estrogen receptor alpha- and beta-positive cells in adult male and female mouse intestine at various estrogen levels. Histochem. Cell. Biol. 121, 399–405. doi: 10.1007/s00418-004-0644-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y. S., and Kim, N. (2018). Sex-gender differences in irritable bowel syndrome. J. Neurogastroenterol. Motil. 24, 544–558. doi: 10.5056/jnm18082

PubMed Abstract | CrossRef Full Text | Google Scholar

Klatt, P., Schmidt, K., Uray, G., and Mayer, B. (1993). Multiple catalytic functions of brain nitric oxide synthase. Biochemical characterization, cofactor-requirement, and the role of N omega-hydroxy-L-arginine as an intermediate. J. Biol. Chem. 268, 14781–14787. doi: 10.1016/s0021-9258(18)82401-2

CrossRef Full Text | Google Scholar

Kleinert, H., Wallerath, T., Euchenhofer, C., Ihrig-Biedert, I., Li, H., and Forstermann, U. (1998). Estrogens increase transcription of the human endothelial NO synthase gene: analysis of the transcription factors involved. Hypertension 31, 582–588. doi: 10.1161/01.hyp.31.2.582

CrossRef Full Text | Google Scholar

Lam, K. K., Lee, Y. M., Hsiao, G., Chen, S. Y., and Yen, M. H. (2006). Estrogen therapy replenishes vascular tetrahydrobiopterin and reduces oxidative stress in ovariectomized rats. Menopause 13, 294–302. doi: 10.1097/01.gme.0000182806.99137.5e

CrossRef Full Text | Google Scholar

Li, Y., Xu, J., Jiang, F., Jiang, Z., Liu, C., Li, L., et al. (2016). G protein-coupled estrogen receptor is involved in modulating colonic motor function via nitric oxide release in C57BL/6 female mice. Neurogastroenterol. Motil. 28, 432–442. doi: 10.1111/nmo.12743

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J. Y. H., Lin, G., Fang, M., and Rudd, J. A. (2019). Localization of estrogen receptor ERalpha, ERbeta and GPR30 on myenteric neurons of the gastrointestinal tract and their role in motility. Gen. Comp. Endocrinol. 272, 63–75. doi: 10.1016/j.ygcen.2018.11.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Lyster, D. J., Bywater, R. A., and Taylor, G. S. (1995). Neurogenic control of myoelectric complexes in the mouse isolated colon. Gastroenterology 108, 1371–1378. doi: 10.1016/0016-5085(95)90684-3

CrossRef Full Text | Google Scholar

Maggi, A., Ciana, P., Belcredito, S., and Vegeto, E. (2004). Estrogens in the nervous system: mechanisms and nonreproductive functions. Annu. Rev. Physiol. 66, 291–313. doi: 10.1146/annurev.physiol.66.032802.154945

PubMed Abstract | CrossRef Full Text | Google Scholar

Mayer, E. A., Naliboff, B., Lee, O., Munakata, J., and Chang, L. (1999). Review article: gender-related differences in functional gastrointestinal disorders. Aliment Pharmacol. Ther. 13, 65–69. doi: 10.1046/j.1365-2036.1999.00008.x

PubMed Abstract | CrossRef Full Text | Google Scholar

McEwen, B. S., and Alves, S. E. (1999). Estrogen actions in the central nervous system. Endocr. Rev. 20, 279–307. doi: 10.1210/er.20.3.279

CrossRef Full Text | Google Scholar

McNeill, A. M., Zhang, C., Stanczyk, F. Z., Duckles, S. P., and Krause, D. N. (2002). Estrogen increases endothelial nitric oxide synthase via estrogen receptors in rat cerebral blood vessels: effect preserved after concurrent treatment with medroxyprogesterone acetate or progesterone. Stroke 33, 1685–1691. doi: 10.1161/01.str.0000016325.54374.93

CrossRef Full Text | Google Scholar

Michel, T., and Vanhoutte, P. M. (2010). Cellular signaling and NO production. Pflugers Arch. 459, 807–816.

Google Scholar

Nation, T., Buraundi, S., Balic, A., Southwell, B., Newgreen, D., and Hutson, J. (2011). Androgen and estrogen receptor expression in the spinal segments of the genitofemoral nerve during testicular descent. J. Pediatr. Surg. 46, 1539–1543. doi: 10.1016/j.jpedsurg.2010.11.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Neal, K. B., and Bornstein, J. C. (2007). Mapping 5-HT inputs to enteric neurons of the guinea-pig small intestine. Neuroscience 145, 556–567. doi: 10.1016/j.neuroscience.2006.12.017

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Mahony, F., Alzamora, R., Betts, V., LaPaix, F., Carter, D., Irnaten, M., et al. (2007). Female gender-specific inhibition of KCNQ1 channels and chloride secretion by 17beta-estradiol in rat distal colonic crypts. J. Biol. Chem. 282, 24563–24573. doi: 10.1074/jbc.m611682200

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Mahony, F., and Harvey, B. J. (2008). Sex and estrous cycle-dependent rapid protein kinase signaling actions of estrogen in distal colonic cells. Steroids 73, 889–894. doi: 10.1016/j.steroids.2008.01.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Palomba, S., Di Cello, A., Riccio, E., Manguso, F., and La Sala, G. B. (2011). Ovarian function and gastrointestinal motor activity. Minerva Endocrinol. 36, 295–310.

Google Scholar

Powell, A. K., and Bywater, R. A. (2001). Endogenous nitric oxide release modulates the direction and frequency of colonic migrating motor complexes in the isolated mouse colon. Neurogastroenterol. Motil. 13, 221–228. doi: 10.1046/j.1365-2982.2001.00260.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Powell, A. K., Fida, R., and Bywater, R. A. (2003). Motility in the isolated mouse colon: migrating motor complexes, myoelectric complexes and pressure waves. Neurogastroenterol. Motil. 15, 257–266.

Google Scholar

Ravella, K., Al-Hendy, A., Sharan, C., Hale, A. B., Channon, K. M., Srinivasan, S., et al. (2013). Chronic estrogen deficiency causes gastroparesis by altering neuronal nitric oxide synthase function. Dig. Dis. Sci. 58, 1507–1515. doi: 10.1007/s10620-013-2610-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Roberts, R. R., Murphy, J. F., Young, H. M., and Bornstein, J. C. (2007). Development of colonic motility in the neonatal mouse-studies using spatiotemporal maps. Am. J. Physiol. 292:G930.

Google Scholar

Ryan, J. P., and Bhojwani, A. (1986). Colonic transit in rats: effect of ovariectomy, sex steroid hormones, and pregnancy. Am. J. Physiol. 251, G46–G50.

Google Scholar

Sang, Q., and Young, H. M. (1996). Chemical coding of neurons in the myenteric plexus and external muscle of the small and large intestine of the mouse. Cell Tissue Res. 284, 39–53. doi: 10.1007/s004410050565

PubMed Abstract | CrossRef Full Text | Google Scholar

Serova, L. I., Filipenko, M., Schilt, N., Veerasirikul, M., and Sabban, E. L. (2006). Estrogen-triggered activation of GTP cyclohydrolase 1 gene expression: role of estrogen receptor subtypes and interaction with cyclic AMP. Neuroscience 140, 1253–1263. doi: 10.1016/j.neuroscience.2006.03.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Shah, S., Hobbs, A., Singh, R., Cuevas, J., Ignarro, L. J., and Chaudhuri, G. (2000). Gastrointestinal motility during pregnancy: role of nitrergic component of NANC nerves. Am. J. Physiol. Regul. Integr. Comp. Physiol. 279, R1478–R1485. doi: 10.1016/s0140-6736(86)92680-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Shah, S., Nathan, L., Singh, R., Fu, Y. S., and Chaudhuri, G. (2001). E2 and not P4 increases NO release from NANC nerves of the gastrointestinal tract: implications in pregnancy. Am. J. Physiol. Regul. Integr. Comp. Physiol. 280, R1546–R1554.

Google Scholar

Showkat Ali, M., Tiscareno-Grejada, I., Locovei, S., Smiley, R., Collins, T., Sarosiek, J., et al. (2012). Gender and estradiol as major factors in the expression and dimerization of nNOSalpha in rats with experimental diabetic gastroparesis. Dig. Dis. Sci. 57, 2814–2825. doi: 10.1007/s10620-012-2230-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Sica, M., Martini, M., Viglietti-Panzica, C., and Panzica, G. (2009). Estrous cycle influences the expression of neuronal nitric oxide synthase in the hypothalamus and limbic system of female mice. BMC Neurosci. 10:78. doi: 10.1186/1471-2202-10-78

PubMed Abstract | CrossRef Full Text | Google Scholar

Spencer, N. J. (2001). Control of migrating motor activity in the colon. Curr. Opin. Pharmacol. 1, 604–610. doi: 10.1016/s1471-4892(01)00103-5

CrossRef Full Text | Google Scholar

Spencer, N. J., Bywater, R. A., Holman, M. E., and Taylor, G. S. (1998). Inhibitory neurotransmission in the circular muscle layer of mouse colon. J. Auton. Nerv. Syst. 70, 10–14. doi: 10.1016/s0165-1838(98)00045-9

CrossRef Full Text | Google Scholar

Sprouse, J. C., Sampath, C., and Gangula, P. R. (2020). Supplementation of 17β-Estradiol normalizes rapid gastric emptying by restoring impaired Nrf2 and nNOS function in obesity-induced diabetic ovariectomized mice. Antioxidants (Basel) 9:582. doi: 10.3390/antiox9070582

PubMed Abstract | CrossRef Full Text | Google Scholar

Swaminathan, M., Hill-Yardin, E., Ellis, M., Zygorodimos, M., Johnston, L. A., Gwynne, R. M., et al. (2016). Video imaging and spatiotemporal maps to analyze gastrointestinal motility in mice. J. Vis. Exp. 108:53828.

Google Scholar

Tamura, K., Schemann, M., and Wood, J. D. (1993). Actions of nitric oxide-generating sodium nitroprusside in myenteric plexus of guinea pig small intestine. Am. J. Physiol. 265, G887–G893.

Google Scholar

Tran, M., Gallo, L. A., Wadley, G. D., Jefferies, A. J., Moritz, K. M., and Wlodek, M. E. (2012). Effect of pregnancy for females born small on later life metabolic disease risk. PLoS One 7:e45188. doi: 10.1371/journal.pone.0045188

PubMed Abstract | CrossRef Full Text | Google Scholar

Tytgat, G. N., Heading, R. C., Müller-Lissner, S., Kamm, M. A., Schölmerich, J., Berstad, A., et al. (2003). Contemporary understanding and management of reflux and constipation in the general population and pregnancy: a consensus meeting. Aliment Pharmacol. Ther. 18, 291–301. doi: 10.1046/j.1365-2036.2003.01679.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Upmacis, R. K., Shen, H., Benguigui, L. E., Lamon, B. D., Deeb, R. S., Hajjar, K. A., et al. (2011). Inducible nitric oxide synthase provides protection against injury-induced thrombosis in female mice. Am. J. Physiol. Heart Circ. Physiol. 301, H617–H624.

Google Scholar

Vasquez-Vivar, J., Hogg, N., Martasek, P., Karoui, H., Pritchard, K. A. Jr., and Kalyanaraman, B. (1999). Tetrahydrobiopterin-dependent inhibition of superoxide generation from neuronal nitric oxide synthase. J. Biol. Chem. 274, 26736–26742. doi: 10.1074/jbc.274.38.26736

PubMed Abstract | CrossRef Full Text | Google Scholar

Weiner, C. P., Lizasoain, I., Baylis, S. A., Knowles, R. G., Charles, I. G., and Moncada, S. (1994). Induction of calcium-dependent nitric oxide synthases by sex hormones. Proc. Natl. Acad. Sci. U S A. 91, 5212–5216.

Google Scholar

Yuan, S. Y., Bornstein, J. C., and Furness, J. B. (1995). Pharmacological evidence that nitric oxide may be a retrograde messenger in the enteric nervous system. Br. J. Pharmacol. 114, 428–432.

Google Scholar

Keywords: estrogen, nitric oxide synthase, enteric neural circuits, colonic motor complexes, ERalpha and ERbeta, immunohistochemistry, neuroplasticity, estrus cycle

Citation: Balasuriya GK, Nugapitiya SS, Hill-Yardin EL and Bornstein JC (2021) Nitric Oxide Regulates Estrus Cycle Dependent Colonic Motility in Mice. Front. Neurosci. 15:647555. doi: 10.3389/fnins.2021.647555

Received: 30 December 2020; Accepted: 12 August 2021;
Published: 29 September 2021.

Edited by:

Jan D. Huizinga, McMaster University, Canada

Reviewed by:

Marcel Jimenez, Universitat Autònoma de Barcelona, Spain
Hongzhen Hu, Washington University in St. Louis, United States
Andreas Friebe, Julius Maximilian University of Würzburg, Germany

Copyright © 2021 Balasuriya, Nugapitiya, Hill-Yardin and Bornstein. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Joel C. Bornstein, j.bornstein@unimelb.edu.au

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.