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接受胰岛素钳夹术的泌乳山羊的蛋白质代谢

Protein metabolism in lactating goats subjected to the insulin clamp.

作者信息

Bequette B J, Kyle C E, Crompton L A, Anderson S E, Hanigan M D

机构信息

Rowett Research Institute, Bucksburn, Aberdeen, Scotland.

出版信息

J Dairy Sci. 2002 Jun;85(6):1546-55. doi: 10.3168/jds.S0022-0302(02)74224-0.

DOI:10.3168/jds.S0022-0302(02)74224-0
PMID:12146487
Abstract

A model of Leu and protein metabolism by the mammary gland and hind leg of lactating goats was constructed and evaluated from data collected by using [15N, 1-13C]Leu kinetics measured during amino acid (AA) infusion and a hyperinsulinemic-euglycemic clamp (IC). Goats were given continuous intravenous infusions of either saline or AA (65 g/d) for 7.5 d and from d 5 to 7.5 goats were subjected to IC. Arteriovenous kinetics were monitored on d 4 and 8 by continuous infusion (8 h) of [15N, 1-13C]Leu. Milk protein yield was increased by IC (+10%) and IC +AA (+21%), whereas AA infusion had no effect. The data were used to construct model equations that describe rates of protein synthesis and degradation, and from these equations, milk and muscle net protein synthesis were described. The model was unable to describe the observed responses in milk protein synthesis. Similar to observations in the literature, net protein gain by the hind leg increased with AA, IC, and IC + AA infusion, primarily through stimulation of protein synthesis by AA. For both tissues, IC depressed Leu oxidation, but only in the absence of AA infusion. Although the IC appears to regulate the ability of the mammary gland to coordinate blood flow and Leu catabolism in support of protein synthesis, our ability to construct a precise model describing mammary protein anabolism is still limited. In contrast, the response in protein anabolism of the hind-leg tissues of these midlactation goats was predicted well by the model, which indicate that the leg tissues were more sensitive to AA supply than the mammary gland.

摘要

利用氨基酸(AA)输注和高胰岛素-正常血糖钳夹(IC)期间测得的[15N, 1-13C]亮氨酸动力学数据,构建并评估了泌乳山羊乳腺和后肢的亮氨酸及蛋白质代谢模型。给山羊连续静脉输注生理盐水或AA(65 g/d),持续7.5天,从第5天到第7.5天对山羊进行IC。在第4天和第8天,通过连续输注(8小时)[15N, 1-13C]亮氨酸监测动静脉动力学。IC(增加10%)和IC + AA(增加21%)可提高乳蛋白产量,而AA输注则无影响。这些数据用于构建描述蛋白质合成和降解速率的模型方程,并根据这些方程描述乳汁和肌肉的净蛋白质合成。该模型无法描述观察到的乳蛋白合成反应。与文献中的观察结果相似,后肢的净蛋白质增加量随着AA、IC和IC + AA输注而增加,主要是通过AA刺激蛋白质合成。对于这两种组织,IC均降低了亮氨酸氧化,但仅在无AA输注时出现这种情况。尽管IC似乎调节了乳腺协调血流和亮氨酸分解代谢以支持蛋白质合成的能力,但我们构建精确描述乳腺蛋白质合成代谢模型的能力仍然有限。相比之下,该模型很好地预测了这些泌乳中期山羊后肢组织蛋白质合成代谢的反应,这表明后肢组织比乳腺对AA供应更敏感。

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Protein metabolism in lactating goats subjected to the insulin clamp.接受胰岛素钳夹术的泌乳山羊的蛋白质代谢
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