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血管活性肠肽和垂体腺苷酸环化酶激活肽刺激牛蛙垂体释放促甲状腺激素。

VIP and PACAP stimulate TSH release from the bullfrog pituitary.

作者信息

Okada Reiko, Yamamoto Kazutoshi, Ito Yoichi, Mochida Hiroshi, Tonon Marie-Christine, Fournier Alain, Leprince Jérôme, Vaudry Hubert, Kikuyama Sakae

机构信息

Department of Biology, School of Education, Waseda University, Tokyo 169-8050, Japan.

出版信息

Peptides. 2007 Sep;28(9):1784-9. doi: 10.1016/j.peptides.2007.03.012. Epub 2007 Mar 30.

Abstract

We have recently shown that corticotropin-releasing hormone (CRH) is a major thyrotropin (TSH)-releasing factor in amphibians, but we have also found that, besides CRH, other hypothalamic substances stimulate TSH secretion in frog. In order to characterize novel TSH secretagogues, we have investigated the effect of frog (Rana ridibunda) vasoactive intestinal polypeptide (VIP) (fVIP) and pituitary adenylate cyclase-activating polypeptide (PACAP) (fPACAP38 and PACAP27) on TSH release from bullfrog (Rana catesbeiana) pituitary cells in primary culture. Incubation of pituitary cells for 24h with graded concentrations of fVIP, fPACAP38 and PACAP27 (10(-9) to 10(-6)M) induced a dose-dependent stimulation of TSH release with minimum effective doses of 10(-9)M for fVIP and 10(-8)M for fPACAP38 and PACAP27. The PAC1-R/VPAC2-R antagonist PACAP(6-38) (10(-7) and 10(-6)M) dose-dependently suppressed the stimulatory effects of fVIP and fPACAP38 (10(-7)M each). Likewise, this antagonist (10(-6) and 10(-5)M) dose-dependently attenuated the stimulatory effect of PACAP27 (10(-7)M). On the other hand, the VPAC1-R/VPAC2-R antagonist [d-pCl-Phe(6), Leu(17)]VIP (10(-6) and 10(-5)M) dose-dependently inhibited the stimulatory effect of fVIP (10(-9)M) and PACAP27 (10(-8)M), but did not affect the response to fPACAP38 (10(-8)M). These data indicate that, in amphibians, the activity of thyrotrophs can be regulated by VIP and PACAP acting likely through VPAC2-R and PAC1-R.

摘要

我们最近发现促肾上腺皮质激素释放激素(CRH)是两栖动物中主要的促甲状腺激素(TSH)释放因子,但我们也发现,除了CRH之外,其他下丘脑物质也能刺激青蛙的TSH分泌。为了鉴定新的TSH促分泌素,我们研究了青蛙(食用蛙)血管活性肠肽(VIP)(fVIP)和垂体腺苷酸环化酶激活肽(PACAP)(fPACAP38和PACAP27)对原代培养的牛蛙(牛蛙)垂体细胞释放TSH的影响。用梯度浓度的fVIP、fPACAP38和PACAP27(10^(-9)至10^(-6)M)孵育垂体细胞24小时,可诱导TSH释放呈剂量依赖性刺激,fVIP的最小有效剂量为10^(-9)M,fPACAP38和PACAP27的最小有效剂量为10^(-8)M。PAC1-R/VPAC2-R拮抗剂PACAP(6 - 38)(10^(-7)和10^(-6)M)剂量依赖性地抑制fVIP和fPACAP38(各10^(-7)M)的刺激作用。同样,该拮抗剂(10^(-6)和10^(-5)M)剂量依赖性地减弱PACAP27(10^(-7)M)的刺激作用。另一方面,VPAC1-R/VPAC2-R拮抗剂[d-pCl-Phe(6), Leu(17)]VIP(10^(-6)和10^(-5)M)剂量依赖性地抑制fVIP(10^(-9)M)和PACAP27(10^(-8)M)的刺激作用,但不影响对fPACAP38(10^(-8)M)的反应。这些数据表明,在两栖动物中,促甲状腺细胞的活性可能通过VIP和PACAP作用于VPAC2-R和PAC1-R来调节。

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