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Adenosine regulates the release of adrenocorticotropic hormone (ACTH) from cultured anterior pituitary cells

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Abstract

We have recently shown the presence of adenosine receptors coupled to adenylate cyclase in anterior pituitary and in the present studies we have investigated the effects of adenosine on ACTH release. The ‘R’-site specific analogs of adenosine such as N-Ethylcarboxamide adenosine (NECA), L-N6-phenylisopropyl adenosine (PIA), 2-chloro-adenosine (2-Cl-Ado) all stimulated ACTH release in a dose-dependent manner. NECA was the most potent analog and stimulated ACTH release by about 170% with an apparent Ka of 0.1 µM, whereas PIA and 2-Cl-Ado were less potent and stimulated the release by about 110% and 125% with an apparent Ka of 0.2 and 0.4 µ-M respectively. The stimulation of ACTH release by NECA was inhibited by 3-isobutyl-1-methylxanthine (IBMX). On the other hand, adenosine deaminase (ADA) treatment of the cells also stimulated ACTH release as well as adenylate cyclase activity by about 2-fold, suggesting that endogenous adenosine plays an inhibitory role in the release of ACTH. Other agents, such as corticotropin-releasing factor (CRF), vasoactive intestinal peptide (VIP) and forskolin (FSK) also stimulated ACTH release from these cells. In addition, the stimulation by an optimal concentration of NECA was almost additive with maximal stimulation caused by VIP and FSK. These data suggest that adenosine modulates ACTH release from anterior pituitary through its interaction with adenosine receptors coupled to adenylate cyclase.

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Abbreviations

NECA:

N-Ethylcarboxamideadenosine

PIA:

L-N6-Phenylisopropyladenosine

2-Cl-Ado:

2-chloroadenosine

FSK:

Forskolin

VIP:

Vasoactive Intestinal Peptide

CRF:

Corticotropin Releasing Factor

ADA:

Adenosine Deaminase

IBMX:

3-Isobutyl-1-methylxanthine

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Anand-Srivastava, M.B., Cantin, M. & Gutkowska, J. Adenosine regulates the release of adrenocorticotropic hormone (ACTH) from cultured anterior pituitary cells. Mol Cell Biochem 89, 21–28 (1989). https://doi.org/10.1007/BF00228276

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  • DOI: https://doi.org/10.1007/BF00228276

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