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Projection of ventrolateral medullary (A1) catecholamine neurons toward nucleus tractus solitarii

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Summary

The distribution and interconnections of brainstem catecholamine cell groups thought to be important in cardiovascular control were studied using histochemical and ultrastructural techniques in the rabbit. Lesions and microinjections of horseradish peroxidase (HRP) were made in the nucleus tractus solitarii in the dorsomedial medulla, and in the ventrolateral medulla. After lesions of the dorsomedial medulla the fluorescence intensity of the Al-group of catecholamine neurons was increased, and swollen axons could be seen coursing from the ventrolateral medulla toward the lesions on the same side, but not the opposite side. Most of these axons ran in a band about 2 mm in width, centered at the level of the obex. Electron microscopically, specific cells, identified as A1-catecholamine neurons, showed evidence of chromatolysis after the dorsomedial lesions. Following injection of HRP into the nucleus tractus solitarii, A1-catecholamine cells in the ventrolateral medulla on the same side contained the reaction product. Lesions of the ventrolateral medulla did not produce evidence of a reciprocal projection of A2-catecholamine neurons toward the ventrolateral medulla.

Thus axons of the A1-group of catecholamine neurons in the ventrolateral medulla project toward the ipsilateral nucleus tractus solitarii in a relatively compact band at the level of the obex. On the other hand, the A2-group of catecholamine neurons in the dorsomedial medulla does not appear to send projections toward the A1-group.

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References

  • Blessing WW, Chalmers JP, Howe PRC (1978a) Distribution of catecholamine-containing cell bodies in the rabbit central nervous system. J Comp Neurol 179:407–424

    Google Scholar 

  • Blessing WW, Furness JB, Costa M, Chalmers JP (1978b) Localisation of catecholamine fluorescence and retrogradely transported horseradish peroxidase within the same nerve cell. Neurosci Lett 9:311–315

    Google Scholar 

  • Blessing WW, West MJ, Chalmers JP (1979) Hypertension and pulmonary oedema following lesions of catecholamine neurons (A1) in the ventrolateral medulla of the rabbit. Proc AustPhysiol Pharmacol Soc 10:272P

    Google Scholar 

  • Blessing WW, Goodchild AK, Dampney RAL, Chalmers JP (1981) Cell groups in the lower brain stem of the rabbit projecting to the spinal cord, with special reference to catecholamine-containing neurons. Brain Res (in press)

  • Carlsson A, Falck B, Fuxe K, Hillarp N-Å (1964) Cellular localization of monamines in the spinal cord. Acta Physiol Scand 60:112–119

    Google Scholar 

  • Chalmers JP (1975) Brain amines and models of experimental hypertension. Circ Res 36:469–480

    Google Scholar 

  • Chalmers JP (1978) Nervous system and hypertension. Clin Sci Molec Med 55:45s-56s

    Google Scholar 

  • Commissiong JW, Hellstrom SO, Neff NH (1978) A new projection from locus coeruleus to the spinal ventral columns: histochemical and biochemical evidence. Brain Res 148:207–213

    Google Scholar 

  • Coote JH, McLeod VH (1974) The influence of bulbospinal monoaminergic pathways on sympathetic nerve activity. J Physiol 225:44–46P

    Google Scholar 

  • Cottle MK, Calaresu FR (1975) Projections from the nucleus and tractus solitarius in the cat. J Comp Neurol 161:143–158

    Google Scholar 

  • Dahlström A, Fuxe K (1964) Evidence for the existence of monoamine-containing neurons in the central nervous system. I. Demonstration of monoamines in the cell bodies of brain stem neurons. Acta Physiol Scand 62:1–55

    Google Scholar 

  • Dahlström A, Fuxe K (1965) Evidence for the existence of monoamine neurons in the central nervous system. II. Experimentally induced changes in the intraneuronal amine levels of bulbospinal neuron systems. Acta Physiol Scand 64:7–41

    Google Scholar 

  • Day TA, Blessing WW, Willoughby JO (1980) Noradrenergaic and dopaminergic projections to the medial preoptic area of the rat. A combined horseradish peroxidase catecholamine fluorescence study. Brain Res 193:543–548

    Google Scholar 

  • De Jong W, Zandberg P, Bohus B (1975) Central inhibitory noradrenergic cardiovascular control. In: Gispen W, Van Wimersma Greidanus TB, Bohus B, De Wied D (eds) Progress in brain research, Vol 42 Proceedings of the Vth International Congress of the International Society of Neuroendocrinology. Elsevier Scientific Pub, Co. Amsterdam, pp 285–298

    Google Scholar 

  • De Jong W, Zandberg P, Palkovits M, Bohus B (1977) Acute and chronic hypertension after lesions and transections of the rat brain stem. Hypertension and brain mechanisms, Progress in Brain Res 47:181–197

    Google Scholar 

  • Doba N, Reis DJ (1973) Acute fulminating neurogenic hypertension produced by brainstem lesions in the rat. Circ Res 32:584–593

    Google Scholar 

  • Furness JB, Costa M, Blessing WW (1977) Simultaneous fixation and production of catecholamine fluorescence in central nervous tissue by perfusion with aldehydes. Histochem J 9:745–750

    Google Scholar 

  • Furness JB, Heath JW, Costa M (1978) Aqueous aldehyde (Faglu) methods for the fluorescence histochemical localization of catecholamines and for ultrastructural studies of central nervous tissue. Histochemistry 57:285–395

    Google Scholar 

  • Hökfelt T, Fuxe K, Goldstein M, Johansson OI (1974) Immunohistochemical evidence for the existence of adrenaline neurons in the rat brain. Brain Res 66:235–251

    Google Scholar 

  • Howe PRC, Costa M, Furness JB, Chalmers JP (1980) Simultaneous demonstration of PNMT immunofluorescent and catecholamine fluorescent nerve cell bodies in the rat medulla oblongata. Neurosci 5:2229–2238

    Google Scholar 

  • Korner PI (1979) Central nervous control of autonomic cardiovascular function. In: Berne RM, Sperelakis N, Gieger SR (eds) Handbook of Physiology, the cardiovascular system I, Chapter 20. The Williams & Wilkins Company, Baltimore, pp 691–739

    Google Scholar 

  • Loewy AD, McKellar S, Saper CB (1979) Direct projections from the A5 catecholamine cell group to the intermediolateral cell column. Brain Res 174:309–314

    Google Scholar 

  • Mesulam M-M (1978) Tetramethylbenzidine for horseradish peroxidase neurohistochemistry: A noncarcinogenic blue reaction product with superior sensitivity for visulizing neural afferents and efferents. J Histochem Cytochem 26:106–117

    CAS  PubMed  Google Scholar 

  • Morest DK (1967) Experimental study of the projections of the nucleus of the tractus solitarius and the area postrema in the cat. J Comp Neurol 130:277–300

    Google Scholar 

  • Nygren L-G, Olson L (1977) A new major projection from locus coeruleus: the main source of noradrenergic nerve terminals in the ventral and dorsal columns of the spinal cord. Brain Res 132:85–93

    Google Scholar 

  • Palkovits M, Jacobwitz DM (1974) Topographic atlas of catecholamines and acetylcholinesterase-containing neurons in the rat brain. II. Hindbrain (mesencephalon, rhombencephalon). J Comp Neurol 157:29–42

    Google Scholar 

  • Palkovits M, Zaborszky L (1977) Neuroanatomy of central cardiovascular control. Nucleus tractus solitarius: afferent and efferent neuronal connections in relation to the baroreceptor reflex arc. Progress in Brain Res. 47:9–34

    Google Scholar 

  • Reis DJ, Doba N, Snyder DW, Nathan MA (1977) Brain lesions and hypertension: chronic lability and elevation of arterial pressure produced by electrolytic lesions and 6-hydroxydopamine treatment in nucleus tractus solitarii (NTS) in rats and cats. Progress in Brain Res 47:169–188

    Google Scholar 

  • Reis DJ, Joh TH, Nathan MA, Renaud B, Snyder DW, Talman WT (1979) Nucleus tractus solitarii: catecholaminergic innervation in normal and abnormal control of arterial pressure. In: Schmidt H, Meyer P (eds) Nervous system and hypertension. Wiley, New York, pp 147–164

    Google Scholar 

  • Sakai K, Touret M, Salvert D, Leger L, Jouvet M (1977) Afferent projections to the cat locus coeruleus as visualised by the horseradish peroxidase technique. Brain Res 119:21–41

    Google Scholar 

  • Sakumoto T, Tohyama M, Satoh K, Kimoto Y, Kinugasa T, Tanizawa O, Kurachi K, Shimizu N (1978) Afferent connections from lower brain stem to hypothalamus studied by the horseradish peroxidsase method with special reference to noradrenaline innervation. Exp Brain Res 31:81–84

    Google Scholar 

  • Swanson LW, Hartman BK (1975) The central adrenergic system. An immunofluorescence study of the location of cell bodies and their efferent connections in the rat utilizing dopamine-β-hydroxylase as a marker. J Comp Neurol 163:467–505

    Google Scholar 

  • Ungerstedt U (1971) Stereotaxic mapping of the monoamine pathways in the rat brain. Acta Physiol Scand 367:1–48

    CAS  PubMed  Google Scholar 

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These studies were supported by grants from the National Heart Foundation of Australia and The Life Insurance Medical Research Fund of Australia and New Zealand, and Merck Sharp and Dohme (Australia) Pty Limited

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Blessing, W.W., Furness, J.B., Costa, M. et al. Projection of ventrolateral medullary (A1) catecholamine neurons toward nucleus tractus solitarii. Cell Tissue Res. 220, 27–40 (1981). https://doi.org/10.1007/BF00209963

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