Effect of Paraventricular Lesions on Corticotropin-Releasing Factor (CRF)-Like Immunoreactivity in the Stalk-Median Eminence: Studies on the Adrenocorticotropin Response to Ether Stress and Exogenous CRF*
- 1 January 1984
- journal article
- research article
- Published by The Endocrine Society in Endocrinology
- Vol. 114 (1) , 57-62
- https://doi.org/10.1210/endo-114-1-57
Abstract
Corticotropin-releasing factor-like immunoreactivity (CRF) and plasma ACTH were measured in rats bearing bilateral lesions of the paraventricular nucleus (PVN). Four to 6 days after stereotaxic surgery, CRF-like immunoreactivity content of the stalk-median eminence was reduced by 87-90% and the ACTH response to a 3-min ether stress was greatly attenuated (70-85% reduction). In order to differentiate between possible effects of CRF, catecholamines and arginine-vasopression (AVP), the following treatments were used: group I, sham/vehicle; group II, sham/AVP-antagonist; group III, sham/ganglionic blocker chorisondamine; group IV, PVN-lesions/vehicle; group V, PVN-lesion/AVP antagonist; group VI, PVN-lesion/chlorisondamine. Blood was sampled at 0, 5 and 15 min after a 3-min exposure to ether vapor. PVN lesions alone greatly attenuated the ACTH response to ether stress by 70-85% (group IV); basal ACTH levels were not affected. Chlorisondamine alone (group III) was as effective as PVN lesions in reducing the secretion of ACTH due to stress. When PVN-lesioned animals were treated with the ganglionic blocker, the residual ACTH response was completely abolished (group VI). The AVP-antagonist alone reduced the response at +15 min by 45%; the antagonist given to PVN-lesioned animals completely abolished the response at 15 min. Injection of 0.15 nmol ovine CRF into PVN-lesioned rats resulted in a dramatically increased ACTH response (328% at 15 min) in comparison to the response of sham-operated rats. CRF originating from neurons within the PVN is the predominant regulator of stress-induced ACTH secretion; catecholamines and AVP are involved in mediating stress-induced ACTH secretion, most probably as CRF-potentiating agents; and pituitary hyperresponsiveness to exogenous CRF results from removal of endogenous CRF.This publication has 27 references indexed in Scilit:
- Characterization of a 41-Residue Ovine Hypothalamic Peptide That Stimulates Secretion of Corticotropin and β-EndorphinScience, 1981
- Characteristics of the α-Adrenergic Stimulation of Adrenocorticotropin Secretion in Rat Anterior Pituitary CellsEndocrinology, 1981
- Effects of paraventricular lesions on stimulated ACTH release and CRF in stalk-median eminence of the ratAmerican Journal of Physiology-Endocrinology and Metabolism, 1981
- Control of Release of Adrenocorticotropin and Vasopressin by the Supraoptic and Paraventricular Nuclei*Endocrinology, 1981
- CORTICOTROPHIN RELEASING ACTIVITY IN EXTRACTS OF THE STALK MEDIAN EMINENCE OF BRATTLEBORO RATSJournal of Endocrinology, 1980
- Reevaluation of the Pituitary-Adrenal Response to Ether in Rats with Various Cuts Around the Medial Basal HypothalamusNeuroendocrinology, 1980
- Design of potent antagonists of the vasopressor response to arginine-vasopressinJournal of Medicinal Chemistry, 1978
- A general procedure for estimation of corticosteroid response in individual ratsSteroids, 1978
- Pulsatile growth hormone, prolactin, and thyrotropin secretion in rats with hypothalamic deafferentationBrain Research, 1977
- Corticotropin Releasing Factor Distribution in Normal and Brattleboro Rat Brain, and Effect of Deafferentation, Hypophysectomy and Steroid Treatment in Normal AnimalsEndocrinology, 1977