Identification of multiple opiate receptors through neuroendocrine responses. I. Effects of agonists.

نویسندگان

  • R Pechnick
  • R George
  • R E Poland
چکیده

The effects of the systemic administration of three prototypic multiple opiate receptor agonists, morphine sulfate (MS), ethylketocyclazocine methanesulfonate (EKC) and N-allylnormetazocine hydrochloride (NANMT), on the release of anterior pituitary hormones were studied in the rat. The serum levels of corticosterone, growth hormone, prolactin and luteinizing hormone were measured by radioimmunoassay 30 min after s.c. injection of the drugs. The three opiate compounds elicited different patterns of release of the four hormones. MS, EKC and NANMT elicited rises in the serum levels of corticosterone whereas only MS and EKC induced elevations in growth hormone. MS stimulated but NANMT inhibited the release of prolactin. The administration of the lowest dose of EKC stimulated the release of prolactin whereas higher doses were without effect suggesting biphasic dose-response relationship. The administration of MS, EKC and the highest dose of NANMT elicited a fall in serum luteinizing hormone levels suggesting that NANMT possesses agonist activity at the receptor mediating luteinizing hormone release. The data support the hypothesis that multiple opiate receptors are involved in the mechanism of action of opiate-induced changes in anterior pituitary hormone release.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Effects of selective dopamine receptor (Dl and D2) agonists on stress-induced gastric ulcer in rat

  It has been revealed that dopamine (DA) modulates gastro-duodenal responses to stress. Several investigations have been made to identify the mechanisms and/or receptors by which DA or its promoters exert their gastroprotective function against stress, however there are many discrepancies in this respect. In order to clarify the relative contribution and/or interaction of two DA receptor subty...

متن کامل

Presence of prejunctional D2-dopaminoceptors and α2-adrenoceptors on the cholinergic nerve of the common bile duct of guinea pig

On most adrenergic and cholinergic nerve terminals, prejunctional α-adrenoceptors belonging to the α2-subtype have been identified. Activation of these receptors will decrease the release of norepinephrine. It has been reported that several isolated tissue preparations contain prejunctional dopamine receptors, the stimulation of which inhibits neurotransmission. It has remained uncertain whethe...

متن کامل

Effects of three beta adrenergic receptor agonists on growth performance, blood biochemical parameters, fatty acids composition and carnitine palmitoyltransferase I gene expression of rainbow trout, Oncorhynchus mykiss

Different beta 1 and 2 adrenergic receptors agonists might have various biological and physiological effects on fish species. An experiment was designed to study the effects of feeding ractopamine, terbutaline and metaproterenol; as beta1, beta2 and less selective beta2 adrenergic receptor agonists, respectively; on body weight gain, feed conversion rate, concentration of biochemical parameters...

متن کامل

Involvement of central opiate receptors in modulation of centrally administered oxytocin-induced antinociception

Objective(s): Oxytocin is involved in modulation of many brain-mediated functions. In the present study, we investigated the central effects of oxytocin and its receptor antagonist, atosiban on inflammatory pain. The contribution of opiate receptors was explored using non-selective and selective antagonists. Materials and Methods: The fourth ventricle of the brain of anesthetized rats was impla...

متن کامل

Multiple opiate receptors in the guinea pig enteric nervous system: unmasking the copresence of receptor subtypes.

Experiments were performed in order to obtain physiological evidence for the presence of delta opioid receptors in the guinea pig isolated ileum. The nonequilibrium narcotic antagonists beta-chlornaltrexamine (beta-CNA) and beta-funaltrexamine (beta-FNA) differentially affected inhibitory responses to mu- and delta-specific opiate ligands (q value). These results indicate that these agonists do...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of pharmacology and experimental therapeutics

دوره 232 1  شماره 

صفحات  -

تاریخ انتشار 1985