Central administration of vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide differentially regulates energy metabolism in chicks

被引:17
|
作者
Tachibana, Tetsuya
Oikawa, Daichi
Adachi, Nami
Boswell, Tim
Furuse, Mitsuhiro
机构
[1] Kyushu Univ, Fac Agr, Div Anim & Marine Bioresource Sci, Lab Adv Anim & Marine Bioresources, Fukuoka 8128581, Japan
[2] Univ Newcastle, Div Biol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
日本学术振兴会;
关键词
chicks; energy expenditure; intracerebroventricular injection; pituitary adenylate cyclase-activating polypeptide; plasma constituents; rectal temperature; vasoactive intestinal peptide;
D O I
10.1016/j.cbpa.2006.12.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vasoactive intestinal peptide (VIP) and pituitary adenylate cyclase-activating polypeptide (PACAP) are the members of the glucagon superfamily and bind to common receptors while PACAP also acts via the PACAP-specific receptor, PAC1. The aim of the present study was to investigate whether intracerebroventricular (ICV) injection of VIP and PACAP acts in a similar or different manner to affect body temperature and energy expenditure in the domestic chick. ICV injection of VIP did not significantly affect rectal temperature, but decreased energy expenditure. On the other hand, ICV injection of PACAP significantly increased both body temperature and energy expenditure. These specific actions of PACAP could be explained by an interaction with the PAC1 receptor, since they were partly, but not entirely, attenuated by PACAP (6-38), a PAC1 receptor antagonist. In addition, it was observed that central administration of both VIP and PACAP induced a reduction in respiratory quotient and increased plasma non-esterified fatty acid concentrations. This suggests that both peptides act centrally to regulate a catabolic response. In summary, brain VIP and PACAP both appear to exert generally catabolic effects on energy metabolism in the chick, but their influence on body temperature and glucose metabolism differs and their central effects do not appear to be mediated by the same receptors. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 164
页数:9
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