The central amygdala modulates hypothalamic-pituitary-adrenal axis responses to systemic interleukin-1β administration

Neuroscience

Volumn 94, Issue 1, 1999, Pages 175-183

  Xu, Y ^a   Day, T A ^a   Buller, K M ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Bed nucleus of the stria terminalis; Brainstem catecholamine cells; Central amygdala; Corticotropin releasing factor; Hypothalamic pituitary adrenal axis; Interleukin 1

Indexed keywords

CORTICOTROPIN RELEASING FACTOR RECEPTOR; IBOTENIC ACID; OXYTOCIN; PROTEIN C FOS; RECOMBINANT INTERLEUKIN 1BETA;

AMYGDALOID NUCLEUS; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CATECHOLAMINE RELEASE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; HYPOTHALAMUS HYPOPHYSIS ADRENAL SYSTEM; IMMUNOHISTOCHEMISTRY; MALE; MICROPHOTOGRAPHY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; SOLITARY TRACT NUCLEUS;

ADRENOCORTICOTROPIC HORMONE; AMYGDALA; ANIMALS; CORTICOTROPIN-RELEASING HORMONE; DENERVATION; EPINEPHRINE; EXCITATORY AMINO ACID AGONISTS; HYPOTHALAMO-HYPOPHYSEAL SYSTEM; IBOTENIC ACID; INTERLEUKIN-1; MALE; NEURONS; NOREPINEPHRINE; OXYTOCIN; PARAVENTRICULAR HYPOTHALAMIC NUCLEUS; PITUITARY-ADRENAL SYSTEM; PROTO-ONCOGENE PROTEINS C-FOS; RATS; RATS, WISTAR; SEPTAL NUCLEI; SOLITARY NUCLEUS;

EID: 0032880720     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(99)00311-5     Document Type: Article

References (57)

1. Beaulieu S., Di Paolo T., Barden N. Control of ACTH secretion by the central nucleus of the amygdala: implication of the serotoninergic system and its relevance to the glucocorticoid delayed negative feedback mechanism. Neuroendocrinology. 44:1986;247-254.
2. Beaulieu S., Di Paolo T., Cote J., Barden N. Participation of the central amygdaloid nucleus in the response of adrenocorticotropin secretion to immobilization stress: opposing roles of the noradrenergic and dopaminergic systems. Neuroendocrinology. 45:1987;37-46.
3. Berk M.L., Finkelstein J.A. Afferent projections to the preoptic area and hypothalamic regions in the rat brain. Neuroscience. 6:1981;1601-1624.
4. Berkenbosch F., Oers J.V., Rey A.D., Tilders F., Besedovsky H. Corticotropin-releasing factor producing neurons in the rat activated by interleukin-1. Science. 238:1987;524-526.
5. Bhatnagar S., Dallman M. Neuroanatomical basis for facilitation of hypothalamic-pituitary-adrenal responses to a novel stressor after chronic stress. Neuroscience. 84:1998;1025-1039.
6. Breder C.D., Saper C.B. Expression of inducible cyclooxygenase mRNA in the mouse brain after systemic administration of bacterial lipopolysaccharide. Brain Res. 713:1996;64-69.
7. Buller K. M., Smith D. W. and Day T. A. (1999) Differential recruitment of hypothalamic neuroendocrine and ventrolateral medulla catecholamine cells by non-hypotensive and hypotensive hemorrhages. Brain Res. (in press).
8. Buller K.M., Xu Y., Day T.A. Indomethacin attenuates oxytocin and hypothalamic-pituitary-adrenal axis responses to systemic interleukin-1β J. Neuroendocr. 10:1998;519-528.
9. Cao C., Matsumura K., Yamagata K., Watanabe Y. Endothelial cells of the rat brain vasculature express cyclooxygenase-2 mRNA in response to systemic interleukin-1 beta: a possible site of prostaglandin synthesis responsible for fever. Brain Res. 733:1996;263-272.
10. Chuluyan H.E., Saphier D., Rohn W.M., Dunn A.J. Noradrenergic innervation of the hypothalamus participates in adrenocortical responses to interleukin-1. Neuroendocrinology. 56:1992;106-111.
11. Cirino M., Renaud L.P. Influence of lateral septum and amygdala stimulation on the excitability of hypothalamic supraoptic neurons. An electrophysiological study in the rat. Brain Res. 326:1985;357-361.
12. Cullinan W.E., Herman J.P., Watson S.J. Ventral subicular interactions with the hypothalamic paraventricular nucleus: evidence for a relay in the bed nucleus of the stria terminalis. J. comp. Neurol. 332:1993;1-20.
13. Cunningham E.T. Jr., Bohn M.C., Sawchenko P.E. Organization of adrenergic inputs to the paraventricular and supraoptic nuclei of the hypothalamus in the rat. J. comp. Neurol. 292:1990;651-667.
14. Cunningham E.T. Jr., Sawchenko P.E. Anatomical specificity of noradrenergic inputs to the paraventricular and supraoptic nuclei of the rat hypothalamus. J. comp. Neurol. 274:1988;60-76.
15. Dayas C. V., Buller K. M. and Day T. A. (1999) Neuroendocrine responses to an emotional stressor: evidence for involvement of the medial but not the central amygdala. Eur. J. Neurosci. (in press).
16. Dunn J.D. Plasma corticosterone responses to electrical stimulation of the bed nucleus of the stria terminalis. Brain Res. 407:1987;327-331.
17. Elmquist J.K., Breder C.D., Sherin J.E., Scammell T.E., Hickey W.F., Dewitt D., Saper C.B. Intravenous lipopolysaccharide induces cyclooxygenase 2-like immunoreactivity in rat brain perivascular micoplia and meningeal macrophages. J. comp. Neurol. 381:1997;119-129.
18. Ericsson A., Arias C., Sawchenko P.E. Evidence for an intramedullary prostaglandin-dependent mechanism in the activation of stress-related neuroendocrine circuitry by intravenous interleukin-1. J. Neurosci. 17:1997;7166-7179.
19. Ericsson A., Kovacs K.J., Sawchenko P.E. A functional anatomical analysis of central pathways subserving the effects of interleukin-1 on stress-related neuroendocrine neurons. J. Neurosci. 14:1994;897-913.
20. Feldman S., Conforti N., Itzik A., Weidenfeld J. Differential effect of amygdaloid lesions on CRF-41, ACTH and corticosterone responses following neural stimuli. Brain Res. 658:1994;21-26.
21. Feldman S., Conforti N., Saphier D. The preoptic area and bed nucleus of the stria terminalis are involved in the effects of the amygdala on adrenocortical secretion. Neuroscience. 37:1990;775-779.
22. Gibbs D.M. Dissociation of oxytocin, vasopressin and corticotropin secretion during different types of stress. Life Sci. 35:1984;487-491.
23. Gray T.S., Carney M.E., Magnuson D.J. Direct projections from the central amygdaloid nucleus to the hypothalamic paraventricular nucleus: possible role in stress-induced adrenocorticotropin release. Neuroendocrinology. 50:1989;433-446.
24. Gray T.S., Piechowski R.A., Yracheta J.M., Rittenhouse P.A., Bethea C.L., Van de Kar L.D. Ibotenic acid lesions in the bed nucleus of the stria terminalis attenuate conditioned stress-induced increases in prolactin, ACTH and corticosterone. Neuroendocrinology. 57:1993;517-524.
25. Harbuz M.S., Chowdrey H.S., Jessop D.S., Biswas S., Lughtman S.L. Role of catecholamines in mediating messenger RNA and hormonal responses to stress. Brain Res. 551:1991;52-57.
26. Herman J.P., Cullinan W.E., Watson S.J. Involvement of the bed nucleus of the stria terminalis in tonic regulation of paraventricular hypothalamic CRH and AVP mRNA expression. J. Neuroendocr. 6:1994;433-442.
27. Hopkins S.J., Rothwell N.J. Cytokines and the nervous system. I: Expression and recognition. Trends Neurosci. 18:1995;83-88.
28. Katsuura G., Gottschall P.E., Dahl R.R., Arimura A. Adrenocorticotropin release induced by intracerebroventricular injection of recombinant human interleukin-1 in rats: possible involvement of prostaglandin. Endocrinology. 122:1988;1773-1779.
29. Kawano H., Masuko S. Caudal ventrolateral medullary neurons projecting to the paraventricular nucleus receive synaptic inputs from the nucleus tractus solitarius: an anterograde and retrograde double-labeling study in the rat. Neurosci. Lett. 218:1996;33-36.
30. Kluger M.J. Fever: role of pyrogens and cryogens. Physiol. Rev. 71:1991;93-127.
31. Marcilhac A., Siaud P. Identification of projections from the central nucleus of the amygdala to the paraventricular nucleus of the hypothalamus which are immunoreactive for corticotrophin-releasing hormone in the rat. Expl Physiol. 82:1997;273-281.
32. Mulders W.H.A.M., Meek J., Hafmans T.G.M., Cools A.R. Plasticity in the stress-regulating circuit: decreased input from the bed nucleus of the stria terminalis to the hypothalamic paraventricular nucleus in Wistar rats following adrenalectomy. Eur. J. Neurosci. 9:1997;2462-2471.
33. Parsadaniantz S.M., Gaillet S., Lenoir V., Batsche E., Barbanel G.E.A. Lesions of the afferent catecholaminergic pathways inhibit the temporal activation of the CRH and POMC gene expression and ACTH release induced by human interleukin-1β in the male rat. Neuroendocrinology. 62:1995;586-595.
34. Petrov T., Jhamandas J.H., Krukoff T.L. Electrical stimulation of the central nucleus of the amygdala induces fos-like immunoreactivity in the hypothalamus of the rat: a quantitative study. Molec. Brain Res. 22:1994;333-340.
35. Petrov T., Krukoff T.L., Jhamandas J.H. Convergent influence of the central nucleus of the amygdala and the paraventricular hypothalamic nucleus upon brainstem autonomic neurons as revealed by c-fos expression and anatomical tracing. J. Neurosci. Res. 42:1995;835-845.
36. Pickel V.M., Van Bockstaele E.J., Chan J., Cestari D.M. Amygdala efferents form inhibitory-type synapses with a subpopulation of catecholaminergic neurons in the rat nucleus tractus solitarius. J. comp. Neurol. 362:1995;510-523.
37. Plotsky P.M. Pathways to the secretion of adrenocorticotropin: a view from the portal. J. Neuroendocr. 3:1991;1-9.
38. Plotsky P.M., Sawchenko P.E. Hypophysial-portal plasma levels, median eminence content and immunohistochemical staining of corticotropin-releasing factor, arginine vasopressin and oxytocin following pharmacological adrenalectomy. Endocrinology. 120:1987;1361-1369.
39. Prewitt C.M., Herman J.P. Lesion of the central nucleus of the amygdala decreases basal CRH mRNA expression and stress-induced ACTH release. Ann. N.Y. Acad. Sci. 746:1994;438-440.
40. Prewitt C.M., Herman J.P. Hypothalamo-pituitary-adrenocortical regulation following lesions of the central nucleus of the amygdala. Stress. 1:1997;263-279.
41. Prewitt C.M.F., Herman J.P. Anatomical interactions between the central amygdaloid nucleus and the hypothalamic paraventricular nucleus of the rat: a dual tract-tracing analysis. J. chem. Neuroanat. 15:1998;173-185.
42. Reis D.J., Gunne L.-M. Brain catecholamines: relation to the defence reaction evoked by brain stimulation in the cat. Science. 15:1965;1768-1770.
43. Rivest S., Rivier C. Influence of the paraventricular nucleus of the hypothalamus in the alteration of neuroendocrine functions induced by physical stress or interleukin. Endocrinology. 129:1991;2049-2057.
44. Rothwell N.J., Hopkins S.J. Cytokines and the nervous system. II: Actions and mechanisms of action. Trends Neurosci. 18:1995;130-136.
45. Saper C.B., Breder C.D. Endogenous pyrogens in the CNS: role in the febrile response. Prog. Brain Res. 93:1992;419-428.
46. Sapolsky R., Rivier C., Yamamoto G., Plotsky P., Vale W.W. Interleukin-1 stimulates the secretion of hypothalamic corticotropin-releasing factor. Science. 238:1987;522-524.
47. Sawchenko P.E. The effects of catecholamine-depleting medullary knife cuts on CRF- and vasopressin-immunoreactivity in the hypothalamus of normal and steroid-manipulated rats. Neuroendocrinology. 48:1988;459-470.
48. Sawchenko P.E., Swanson L.W. The organization of forebrain afferents to the paraventricular and supraoptic nuclei of the rat. J. comp. Neurol. 218:1983;121-144.
49. Smith D.W., Buller K.M., Day T.A. Role of ventrolateral medulla catecholamine cells in hypothalamic neuroendocrine cell responses to systemic hypoxia. J. Neurosci. 15:1995;7979-7988.
50. Smith D.W., Day T.A. Neurochemical identification of Fos-positive neurons using two-colour immunoperoxidase staining. J. Neurosci. Meth. 47:1993;73-83.
51. Sun N., Roberts L., Cassell M.D. Rat central amygdaloid nucleus projections to the bed nucleus of the stria terminalis. Brain Res. Bull. 27:1991;651-662.
52. Uehara A., Gottschall P.E., Dahl R.R., Arimura A. Interleukin-1 stimulates ACTH release by an indirect mechanism which requires endogenous corticotropin releasing factor. Endocrinology. 121:1987;1580-1582.
53. Van de Kar L.D., Piechowski R.A., Rittenhouse P.A., Gray T.S. Amygdaloid lesions: differential effect on conditioned stress and immobilization-induced increases in corticosterone and renin secretion. Neuroendocrinology. 54:1991;89-95.
54. Wallace D.M., Magnuson D.J., Gray T.S. Organization of amygdaloid projections to brainstem dopaminergic, noradrenergic, and adrenergic cell groups in the rat. Brain Res. Bull. 28:1992;447-454.
55. Watanobe H., Nasushita R., Takebe K. A study on the role of circulating prostaglandin E2 in the adrenocorticotropin response to intravenous administration of interleukin-1β in the rat. Neuroendocrinology. 62:1995;596-600.
56. Weidenfeld J., Abramsky O., Ovadia H. Evidence for the involvement of the central adrenergic system in interleukin 1-induced adrenocortical response. Neuropharmacology. 28:1989;1411-1414.
57. Weller K.L., Smith D.A. Afferent connections to the bed nucleus of the stria terminalis. Brain Res. 232:1982;255-270.