Concomitant Changes in the in vitro and in vivo Release of Opioid Peptides and Luteinizing Hormone-Releasing Hormone from the Hypothalamus following Blockade of Receptors for Corticotropin-Releasing Factor
Autor: | Albert Herz, Osborne F. X. Almeida, K.E. Nikolarakis, Dalip J.S. Sirinathsinghji |
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Rok vydání: | 1988 |
Předmět: |
Male
endocrine system medicine.medical_specialty Corticotropin-Releasing Hormone Endocrinology Diabetes and Metabolism Hypothalamus Radioimmunoassay Gonadotropin-releasing hormone Dynorphin In Vitro Techniques Receptors Corticotropin-Releasing Hormone Gonadotropin-Releasing Hormone Cellular and Molecular Neuroscience Corticotropin-releasing hormone Endocrinology Thyrotropin-releasing hormone receptor Internal medicine medicine Animals Opioid peptide Endocrine and Autonomic Systems Chemistry Rats Inbred Strains Peptide Fragments Rats Receptors Neurotransmitter Hormone receptor Endorphins Luteinizing hormone hormones hormone substitutes and hormone antagonists |
Zdroj: | Neuroendocrinology. 47:545-550 |
ISSN: | 1423-0194 0028-3835 |
DOI: | 10.1159/000124967 |
Popis: | In vitro and in vivo perfusion techniques were used to examine the changes in the release of beta-endorphin, methionine-enkephalin (met-enkephalin), dynorphin and luteinizing hormone releasing hormone (LHRH) in response to the corticotropin releasing factor (CRF) receptor antagonist, alpha-helical CRF9-41. All four peptides were measured in the same sample collected at each time interval by specific radioimmunoassay methods. In vitro release experiments were conducted using slices of hypothalami obtained from male rats whereas the in vivo release of these peptides was assessed in push-pull perfusates of the arcuate-median eminence (ARC-ME) region of the medial basal hypothalamus of chloral hydrate-anaesthetized male rats. Treatment of rat hypothalamic slices in vitro with alpha-helical CRF9-41 (10(-6) M) resulted in a significant suppression of the release of beta-endorphin and met-enkephalin within 10 min of application of the antagonist and a coincident significant increase in the release of LHRH. The levels of dynorphin were reduced but these changes were not significant. Within 10 min of withdrawal of the receptor antagonist and perfusion with normal (antagonist-free) medium the levels of these peptides returned to pretreatment values, i.e. the levels of beta-endorphin, met-enkephalin and dynorphin rose while those of LHRH fell. Comparable results were obtained in vivo during push-pull perfusion of the ARC-ME region with alpha-helical CRF9-41.(ABSTRACT TRUNCATED AT 250 WORDS) |
Databáze: | OpenAIRE |
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