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Hippocampal input to a “visceral motor” corticobulbar pathway: an anatomical and electrophysiological study in the rat

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Summary

The hippocampus has previously been shown to influence cardiovascular function, and this effect appears to be mediated by the connection the hippocampus has with the infralimbic area of the medial frontal cortex (MFC), a region which projects directly to the nucleus of the solitary tract (NTS) in the dorsal medulla. In the present study, anatomical and electrophysiological techniques were utilized to determine the degree of convergence of hippocampal input to the MFC on neurons in the MFC which project to the NTS. Injections of the anterograde and retrograde neuroanatomical tracer wheatgerm agglutinin-horseradish peroxidase (WGA-HRP) into the NTS retrogradely labelled cells in the infralimbic and prelimbic regions of the MFC. Injections of WGA-HRP into the ventral hippocampus anterogradely labelled terminals in the MFC which, at the light microscopic level, closely overlapped the origin of the descending projection from the MFC to the brainstem. Electron microscopic analysis revealed that anterogradely labelled terminals make synaptic contact primarily on dendritic processes in the neuropil adjacent to retrogradely labelled cells. In addition, anterogradely labelled terminals did, in some cases, make synaptic contact on the somas of retrogradely labelled cells. Electrical stimulation of the NTS antidromically activated cells in the infralimbic and prelimbic areas of the MFC. The average latency of antidromic activation was 30 msec, corresponding to a conduction velocity of approximately 0.7 m/s. Electrical stimulation of the ventral hippocampus orthodromically activated cells in the MFC. With an appropriate delay between the hippocampal and NTS stimuli, the orthodromic and antidromic potentials could be made to collide. The results of this study establish a structural as well as functional link between the hippocampus and NTS-projection neurons in the MFC.

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References

  • Ben-Ari Y (ed) (1981) The amygdaloid complex. INSERM Symp 20. Elsevier/North-Holland Biomedical Press, Amsterdam

    Google Scholar 

  • Burns SM, Wyss JM (1985) The involvement of the anterior cingulate cortex in blood pressure control. Brain Res 340:71–77

    Article  CAS  PubMed  Google Scholar 

  • Carlsen J (1989) New perspectives on the functional anatomical organization of the basolateral amygdala. Acta Neurol Scand 79:Suppl 122:1–28

    Google Scholar 

  • Carson KA, Mesulam M-M (1982) Electron microscopic demonstration of neural connections using horseradish peroxidase: a comparison of the tetramethylbenzidine procedure with seven other histochemical methods. J Histochem Cytochem 30:425–435

    Google Scholar 

  • Cassell MD, Chittick CA, Siegel MA, Wright DJ (1989) Collateralization of the amygdaloid projections of the rat prelimbic and infralimbic cortices. J Comp Neurol 279:235–248

    Google Scholar 

  • Ferino F, Thierry AM, Glowinski J (1987) Anatomical and electrophysiological evidence for a direct projection from Ammon's horn to the medial prefrontal cortex in the rat. Exp Brain Res 65:421–426

    Google Scholar 

  • Gelsema AJ, Calaresu FR (1987) Chemical microstimulation of the septal area lowers arterial pressure in the rat. Am J Physiol 252:R760-R767

    Google Scholar 

  • Hardy SGP, Holmes DE, Mack SM (1988) Prefrontal stimulusproduced hypotension is blocked by brainstem lidocaine injections. Soc Neurosci Abstr 14:505

    Google Scholar 

  • Hurley KM, Saper CB (1988) Efferent projections from the infralimbic cortex. Soc Neurosci Abstr 14:1319

    Google Scholar 

  • Jay TM, Glowinski J, Thierry A-M (1989) Selectivity of the hippocampal projection to the prelimbic area of the prefrontal cortex in the rat. Brain Res 505:337–340

    Google Scholar 

  • Kosinski RJ, Azizi SA, Mihailoff GA (1988) Convergence of cortico- and cuneopontine projections onto components of the pontocerebellar system in the rat: an anatomical and electrophysiological study. Exp Brain Res 71:541–556

    Google Scholar 

  • Leenen L, Meek J, Nieuwenhuys R (1982) Unmyelinated fibers in the pyramidal tract of the rat: a new view. Brain Res 246:297–301

    Google Scholar 

  • Leenen L, Meek J, Posthuma PR, Nieuwenhuys R (1985) A detailed morphometric analysis of the pyramidal tract of the rat. Brain Res 359:65–80

    Google Scholar 

  • Lipski J (1981) Antidromic activation of neurons as an analytical tool in the study of the central nervous system. J Neurosci Meth 4:1–32

    Google Scholar 

  • Loewy AD, McKellar S (1980) The neuroanatomical basis of central cardiovascular control. Federation Proc 39:2495–2503

    Google Scholar 

  • Lofving B (1961) Cardiovascular adjustments induced from the rostral cingulate gyrus. Acta Physiol Scand 53: Suppl 184:1–84

    Google Scholar 

  • Lovick TA, Coote JH (1988) Electrophysiological properties of paraventriculospinal neurons in the rat. Brain Res 454:123–130

    Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Mesulam M-M (ed) (1982) Tracing neural connections with horseradish peroxidase. John Wiley & Sons, Great Britain

    Google Scholar 

  • Neafsey EJ, Hurley-Gius KM, Arvanitis D (1986) The topographical organization of neurons in the rat medial frontal, insular and olfactory cortex projecting to the solitary nucleus, olfactory bulb, periaqueductal gray and superior colliculus. Brain Res 377:261–270

    CAS  PubMed  Google Scholar 

  • Papez JW (1937) A proposed mechanism of emotion. Arch Neurol Psych 38:725–743

    Google Scholar 

  • Paxinos G, Watson C (1986) The rat brain in stereotaxic coordinates (2nd edn). Academic Press, Sydney

    Google Scholar 

  • Phillips CG, Porter R (1977) Corticospinal neurons: their role in movement. Academic Press, London

    Google Scholar 

  • Porter R, Sanderson JH (1964) Antidromic cortical response to pyramidal tract stimulation in the rat. J Physiol (Lond) 170:355–370

    Article  CAS  Google Scholar 

  • Rogers RC, Fryman DL (1988) Direct connections between the central nucleus of the amygdala and the nucleus of the solitary tract: an electrophysiological study in the rat. J Autonom Nerv Syst 22:83–87

    Google Scholar 

  • Rosene DL, Mesulam M-M (1978) Fixation variables in horseradish peroxidase neurohistochemistry. I. The effects of fixation time and perfusion procedures upon enzyme activity. J Histochem Cytochem 26:28–39

    Google Scholar 

  • Ruit KG, Neafsey EJ (1986) Rat medial frontal cortex single unit responses to electrical stimulation of hippocampus and amygdala. Soc Neurosci Abstr 12:1525

    Google Scholar 

  • Ruit KG, Neafsey EJ (1988) Cardiovascular and respiratory responses to electrical and chemical stimulation of the hippocampus in anesthetized and awake rats. Brain Res 457:310–321

    Google Scholar 

  • Rye DB, Saper CB, Wainer BH (1984) Stabilization of the tetramethylbenzidine (TMB) reaction product: application for retrograde and anterograde tracing, and combination with immunohistochemistry. J Histochem Cytochem 32:1145–1153

    Google Scholar 

  • Sapolsky RM, Krey LC, McEwen BS (1984) Stress down-regulates corticosterone receptors in a site-specific manner in the brain. Endocrinology 114:287–292

    Google Scholar 

  • Swanson LW, Cowan WM (1977) An autoradiographic study of the organization of the efferent connections of the hippocampal formation in the rat. J Comp Neurol 172:49–84

    Google Scholar 

  • Swanson LW (1981) A direct projection from Ammon's horn to prefrontal cortex in the rat. Brain Res 217:150–154

    Google Scholar 

  • Terreberry RR, Neafsey EJ (1983) Rat medial frontal cortex: a visceral motor region with a direct projection to the solitary nucleus. Brain Res 278:245–249

    Google Scholar 

  • Terreberry RR, Neafsey EJ (1984) The effects of medial prefrontal cortex stimulation on heart rate in the awake rat. Soc Neurosci Abstr 10:614

    Google Scholar 

  • Terreberry RR, Neafsey EJ (1987) The rat medial frontal cortex projects directly to autonomic regions of the brainstem. Brain Res Bull 19:639–649

    Google Scholar 

  • Thierry A-M, Tassin JP, Blanc G, Glowinski J (1976) Selective activation of the mesocortical DA system by stress. Nature 263:242–243

    CAS  PubMed  Google Scholar 

  • van der Kooy D, McGinty JF, Koda LY, Gerfen CR, Bloom FE (1982) Visceral cortex: a direct connection from the prefrontal cortex to the solitary nucleus in the rat. Neurosci Lett 33:123–127

    Google Scholar 

  • van der Kooy D, Koda LY, McGinty JF, Gerfen CR, Bloom FE (1984) The organization of projections from the cortex, amygdala, and hypothalamus to the nucleus of the solitary tract in rat. J Comp Neurol 224:1–24

    Google Scholar 

  • Verney C, Baulac M, Berger B, Alvares C, Vigny A, Helles KB (1985) Morphological evidence for a dopaminergic terminal field in the hippocampal formation of young and adult rat. Neuroscience 14:1039–1052

    Google Scholar 

  • Waters RS, Tamai Y, Asanuma H (1985) Caudal cuneate nucleus projection to the direct thalamic relay to the motor cortex: an electrophysiological study. Brain Res 360:361–365

    Google Scholar 

  • Zarzecki P, Wiggin DM (1982) Convergence of sensory inputs upon projection neurons of somatosensory cortex. Exp Brain Res 48:28–42

    Google Scholar 

  • Zerihun L, Harris M (1983) An electrophysiological analysis of caudally projecting neurons from the hypothalamic paraventricular nucleus in the rat. Brain Res 261:13–20

    Google Scholar 

Download references

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Ruit, G., Neafsey, E.J. Hippocampal input to a “visceral motor” corticobulbar pathway: an anatomical and electrophysiological study in the rat. Exp Brain Res 82, 606–616 (1990). https://doi.org/10.1007/BF00228802

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