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血管活性肠肽在催乳素诱导的火鸡孵卵行为控制中的作用。I. 血管活性肠肽的急性输注。

Role of vasoactive intestinal peptide in the control of prolactin-induced turkey incubation behavior. I. Acute infusion of vasoactive intestinal peptide.

作者信息

Pitts G R, Youngren O M, Silsby J L, Foster L K, Foster D N, Rozenboim I, Phillips R E, el Halawani M E

机构信息

Department of Animal Science, University of Minnesota St. Paul 55108.

出版信息

Biol Reprod. 1994 Jun;50(6):1344-9. doi: 10.1095/biolreprod50.6.1344.

Abstract

Vasoactive intestinal peptide (VIP) stimulates prolactin (PRL) secretion. Ovine PRL induces incubation behavior in avian species. This study was designed to determine whether VIP can elevate plasma PRL for up to 3 h. Saline or porcine VIP (pVIP; 30, 60, or 150 ng/min) was infused into the median eminence of laying turkeys for 1 h. The 60- and 150-ng doses of pVIP increased plasma PRL (p < 0.01), whereas the 30-ng dose was insignificant. Pituitary PRL content decreased in pVIP-treated turkeys. Two-hour infusion of 60 or 150 ng chicken VIP (cVIP)/min produced similar elevations of plasma PRL (p < 0.001), which declined within 80 min. Both treatments induced insignificant increases in pituitary PRL mRNA. Saline or cVIP (30, 60, or 60 [pulsed] ng/min) was infused into the median eminence for 3 h. Sixty ng cVIP/min induced the largest PRL release (p < 0.05). The pulsatile and low-cVIP treatments resulted in release of a significant amount of PRL in comparison to the saline treatment (p < 0.01). All cVIP treatments resulted in decreased pituitary PRL content (p < 0.05). The 60-ng dose increased PRL mRNA (p < 0.1). This study shows that 60 ng VIP/min causes the maximum PRL release in laying turkeys. However, pituitary PRL content is depleted and PRL synthesis cannot maintain PRL secretion at high levels.

摘要

血管活性肠肽(VIP)可刺激催乳素(PRL)分泌。绵羊PRL可诱导鸟类的孵卵行为。本研究旨在确定VIP是否能在长达3小时内升高血浆PRL水平。将生理盐水或猪VIP(pVIP;30、60或150 ng/分钟)注入产蛋火鸡的正中隆起1小时。60 ng和150 ng剂量的pVIP可使血浆PRL升高(p < 0.01),而30 ng剂量则无显著影响。pVIP处理的火鸡垂体PRL含量降低。以60或150 ng鸡VIP(cVIP)/分钟的剂量输注2小时可使血浆PRL产生类似的升高(p < 0.001),且在80分钟内下降。两种处理均使垂体PRL mRNA产生无显著意义的增加。将生理盐水或cVIP(30、60或60 [脉冲式] ng/分钟)注入正中隆起3小时。60 ng cVIP/分钟诱导的PRL释放量最大(p < 0.05)。与生理盐水处理相比,脉冲式和低剂量cVIP处理导致大量PRL释放(p < 0.01)。所有cVIP处理均导致垂体PRL含量降低(p < 0.05)。60 ng剂量可使PRL mRNA增加(p < 0.1)。本研究表明,60 ng VIP/分钟可使产蛋火鸡的PRL释放量达到最大。然而,垂体PRL含量减少,PRL合成无法维持高水平的PRL分泌。

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