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在体内多参数生物测定中对甲状旁腺激素拮抗剂的评估。

Evaluation of a parathyroid hormone antagonist in an in vivo multiparameter bioassay.

作者信息

Horiuchi N, Rosenblatt M

出版信息

Am J Physiol. 1987 Aug;253(2 Pt 1):E187-92. doi: 10.1152/ajpendo.1987.253.2.E187.

Abstract

The antagonist properties of a bovine parathyroid hormone analogue ([Tyr34]bPTH-(7-34] amide were quantitatively assessed in vivo in a multiparameter assay to estimate the potency of the antagonist against the major actions of PTH. The analogue inhibited PTH-stimulated urinary excretion of phosphate and adenosine 3',5'-cyclic monophosphate in vitamin D-deficient thyroparathyroidectomized rats in a dose-dependent manner. At a molar dose ratio as low as 5:1 of antagonist to PTH, partial inhibition occurred. PTH stimulates the activity of 25-hydroxyvitamin D3-1 alpha-hydroxylase in renal proximal tubules. When coinfused with PTH, this analogue completely inhibited PTH-stimulated 1 alpha-hydroxylase activity at a molar dose ratio of 25:1 of antagonist to PTH and partially inhibited the activity at a molar dose ratio of 10:1. The analogue revealed no PTH-like agonist activity for stimulation of the 1 alpha-hydroxylase. Taken together, these studies indicate that [Tyr34]bPTH-(7-34) amide is a potent antagonist of several of the parameters of PTH action in vivo and demonstrate the feasibility of designing a PTH antagonist that can interact simultaneously with all the PTH receptors responsible for the hormone's major actions in vivo.

摘要

在一项多参数分析中,对一种牛甲状旁腺激素类似物([Tyr34]bPTH-(7 - 34]酰胺)的拮抗剂特性进行了体内定量评估,以估计该拮抗剂对甲状旁腺激素主要作用的效力。在维生素D缺乏的甲状腺甲状旁腺切除大鼠中,该类似物以剂量依赖性方式抑制甲状旁腺激素刺激的磷酸盐和3',5'-环磷酸腺苷的尿排泄。在拮抗剂与甲状旁腺激素的摩尔剂量比低至5:1时,出现部分抑制。甲状旁腺激素刺激肾近端小管中25-羟基维生素D3-1α-羟化酶的活性。当与甲状旁腺激素共同输注时,该类似物在拮抗剂与甲状旁腺激素的摩尔剂量比为25:1时完全抑制甲状旁腺激素刺激的1α-羟化酶活性,在摩尔剂量比为10:1时部分抑制该活性。该类似物未显示出刺激1α-羟化酶的甲状旁腺激素样激动剂活性。综上所述,这些研究表明,[Tyr34]bPTH-(7 - 34]酰胺是体内甲状旁腺激素作用的几个参数的有效拮抗剂,并证明了设计一种能同时与体内负责该激素主要作用的所有甲状旁腺激素受体相互作用的甲状旁腺激素拮抗剂的可行性。

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