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大鼠垂体神经中间叶的肽类物质在体外刺激生长激素分泌。

Peptides of the neurointermediary lobe of rat pituitary stimulate GH secretion in vitro.

作者信息

Schlegel W, Vecsey A, Eberle A E, Chrétien M, Seidah N G, Zahnd G R

出版信息

Mol Cell Endocrinol. 1983 Sep;32(1):47-55. doi: 10.1016/0303-7207(83)90097-7.

Abstract

alpha-MSH and other fragments of ACTH are potent stimulators of GH release in vivo. The action of such peptides and of extracts of the neurointermediary lobe (NIL) of rat pituitary, a source of endogenous MSH-related peptides, on GH release was investigated in vitro. Peptides with the core sequence of alpha-MSH stimulate GH secretion by primary cultures of rat anterior pituitary cells; however, both the absolute and the relative potencies of these peptides exclude the involvement of melanotropic receptors comparable in specificity to the extrapituitary receptors for these hormones. Extracts of the NIL of rat pituitary stimulate GH release in vitro and the bulk of the releasing activity can be attributed to one (or several) factors with an apparent mass of approx. 10 000 M.W. that can be partially purified by HPLC. The active principle appears to be distinct from both beta-LPH and the human pancreatic GHRF. Thus, while rat NIL contains GH-releasing activity that can be demonstrated in vitro, a direct link to the potent action of MSH-related peptides on GH release in vivo cannot be established, and the action of these peptides in vivo must therefore rely on mechanisms which are not expressed in the in vitro system.

摘要

α-促黑素(α-MSH)及促肾上腺皮质激素(ACTH)的其他片段是体内生长激素(GH)释放的强效刺激物。我们在体外研究了这类肽以及大鼠脑垂体神经中间叶(NIL)提取物(内源性促黑素相关肽的一个来源)对GH释放的作用。具有α-MSH核心序列的肽可刺激大鼠垂体前叶细胞原代培养物分泌GH;然而,这些肽的绝对效力和相对效力均排除了特异性与这些激素的垂体外受体相当的促黑素受体的参与。大鼠垂体NIL提取物在体外刺激GH释放,且大部分释放活性可归因于一种(或几种)表观分子量约为10000的因子,该因子可通过高效液相色谱法(HPLC)进行部分纯化。活性成分似乎与β-促脂素(β-LPH)和人胰腺生长激素释放因子(GHRF)均不同。因此,虽然大鼠NIL含有可在体外证实的GH释放活性,但无法建立其与促黑素相关肽在体内对GH释放的强效作用之间的直接联系,因此这些肽在体内的作用必定依赖于体外系统中未表达的机制。

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