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甲状旁腺激素对人体的脂肪分解作用

On the lipolytic action of parathyroid hormone in man.

作者信息

Sinha T K, Thajchayapong P, Queener S F, Allen D O, Bell N H

出版信息

Metabolism. 1976 Mar;25(3):251-60. doi: 10.1016/0026-0495(76)90083-4.

Abstract

An investigation was carried out to determine whether bovine PTH stimulates lipolysis in human fat tissue, whether this action is mediated by cyclic adenosine 3', 5'-monophosphate and whether the N-terminal 1-34 peptide of bovine PTH is responsible for the lipolytic effect. Studies were also performed to determine if parathyroid extract (PTE) produces lipolysis in normal subjects and in patients with pseudohypoparathyroidism in whom there is a defect in the adenylate system in response to PTH in the renal cortex and presumably in the skeletal system as well. It was found that highly purified bovine PTH in the concentration range between 10(-9) M and 10(-5) M stimulated lipolysis in vitro by human fat in a dose-dependent manner. Significant increases in glycerol production were observed at concentrations of PTH as low as 10(-9) M and maximal increases were seen at 10(-6) M. The hormone significantly increased the concentration of cyclic adenosine 3' ,5'-monophosphate in fat tissue. The synthetic N-terminal 1-34 peptide of bovine PTH was as effective as the native hormone in stimulating glycerol production at a concentration of 10(-9) M-10(-6) M. PTE, 100 mU per kg per min for 30 min given intravenously, produced transient increases in the concentration of plasma free fatty acid in each of eight normal subjects, three patients with hypoparathyroidism and eight patients with pseudohypoparathyroidism. Purified bovine PTH also increased plasma free fatty acid in each of two normal subjects. It is concluded that PTH stimulates lipolysis in human subcutaneous fat, that this action of the hormone is mediated through cyclic adenosine 3', 5'-monophosphate and that the N-terminal 1-34 peptide portion of the hormone is responsible for this lipolytic action. Further, PTE stimulates lipolysis in vivo in man. There appears to be no defect in the adenylate cyclase system in the fat cell in response to PTH in patients with pseudohypoparathyroidism.

摘要

开展了一项研究,以确定牛甲状旁腺激素(PTH)是否刺激人脂肪组织中的脂肪分解,该作用是否由环磷腺苷介导,以及牛PTH的N端1 - 34肽是否是脂肪分解作用的原因。还进行了研究,以确定甲状旁腺提取物(PTE)是否在正常受试者以及假性甲状旁腺功能减退患者中产生脂肪分解作用,在假性甲状旁腺功能减退患者中,肾皮质对PTH的腺苷酸系统存在缺陷,推测骨骼系统也存在缺陷。研究发现,浓度范围在10^(-9) M至10^(-5) M之间的高度纯化牛PTH以剂量依赖方式刺激人脂肪体外脂肪分解。在PTH浓度低至10^(-9) M时,甘油生成量显著增加,在10^(-6) M时达到最大增加。该激素显著增加脂肪组织中环磷腺苷的浓度。牛PTH的合成N端1 - 34肽在浓度为10^(-9) M - 10^(-6) M时,在刺激甘油生成方面与天然激素一样有效。静脉注射PTE,剂量为每千克每分钟100 mU,持续30分钟,在8名正常受试者、3名甲状旁腺功能减退患者和8名假性甲状旁腺功能减退患者中,均使血浆游离脂肪酸浓度产生短暂升高。纯化的牛PTH也使2名正常受试者的血浆游离脂肪酸升高。结论是,PTH刺激人皮下脂肪中的脂肪分解,该激素的这一作用通过环磷腺苷介导,且该激素的N端1 - 34肽部分是这种脂肪分解作用的原因。此外,PTE在人体内刺激体内脂肪分解。假性甲状旁腺功能减退患者的脂肪细胞中腺苷酸环化酶系统对PTH的反应似乎没有缺陷。

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