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Antisera to Vasoactive Intestinal Polypeptide Inhibit Basal Prolactin Release from Dispersed Anterior Pituitary Cells

 

作者: Thad C. Hagen,   Mohammed A. Arnaout,   Wendy J. Scherzer,   Donald R. Martinson,   Thomas L. Garthwaite,  

 

期刊: Neuroendocrinology  (Karger Available online 1986)
卷期: Volume 43, issue 6  

页码: 641-645

 

ISSN:0028-3835

 

年代: 1986

 

DOI:10.1159/000124594

 

出版商: S. Karger AG

 

关键词: Vasoactive intestinal polypeptide;Prolactin;Anti-vasoactive intestinal polypeptide

 

数据来源: Karger

 

摘要:

Vasoactive intestinal polypeptide (VIP) has been identified in hypothalamic tissue, is secreted into hypophysial portal blood, and stimulates prolactin (PRL) release in vivo and in vitro. It has been proposed, therefore, that VIP is a physiologic PRL-releasing factor. In this study, we confirm that VIP stimulates PRL release from rat pituitary cells in vitro, and demonstrate that an anti-VIP antiserum blocks VIP-induced PRL secretion. Surprisingly, the anti-VIP antiserum inhibited basal PRL secretion from rat pituitary cells in 3 separate experiments. Data from these experiments were pooled, as the responses were similar, revealing basal PRL release of 10.7 + 1.3 ng rPRL/105 cells (X ± SE), while anti-VIP antisera significantly inhibited release to 4.4 ±0.6 ng rPRL/105 cells (p < 0.001). PRL release in incubates containing control non-immune sera did not differ from basal release, 8.1 ng rPRL/105 cells. A further control experiment was conducted wherein cells were incubated with an anti-ACTH antiserum, representing another hyperimmune serum, which had no effect on PRL secretion. These data suggest that VIP, in addition to its possible role as a hypothalamic-derived PRL-releasing factor, may play a role within the pituitary as a regulator of basal PRL secretio

 

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