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儿茶酚胺在禁食对大鼠肝脏内皮脂肪酶活性影响中的作用。

Involvement of catecholamines in the effect of fasting on hepatic endothelial lipase activity in the rat.

作者信息

Peinado-Onsurbe J, Soler C, Galan X, Poveda B, Soley M, Llobera M, Ramírez I

机构信息

Departament de Bioquímica i Fisiologia, Universitat de Barcelona, Spain.

出版信息

Endocrinology. 1991 Nov;129(5):2599-606. doi: 10.1210/endo-129-5-2599.

Abstract

The effect of fasting on hepatic endothelial lipase activity in the liver of adult rats was investigated. We found that, both in male and female rats, fasting produced a progressive decrease of the hepatic endothelial lipase activity. Upon refeeding, the activity returned to control values in 48 h. In isolated livers from fed male rats, a sharp peak of hepatic endothelial lipase activity appeared in the perfusate upon heparin addition. It accounted for 75% of the total activity (heparin-released + residual) of the tissue. Fasting (24 h) decreased the heparin-releasable activity, and this effect was responsible for most of the decrease found in whole tissue. We suggest that the effect might be due to a decreased synthesis and/or secretion of the enzyme by hepatocytes, since isolated hepatocytes from fasted rats, incubated at 37 C, released 65% less activity to the incubation medium than hepatocytes from fed rats. Adrenaline, but not insulin, glucagon, dexamethasone, epidermal growth factor, or T3, decreased the amount of hepatic endothelial lipase activity released by hepatocytes isolated from fed rats. The effect of adrenaline appears to be mediated by alpha 1-receptors since phenylephrine but not isoprenaline reproduced, and prazosin but not propranolol blocked, the effect of the catecholamine. In the presence of cycloheximide, adrenaline also decreased the amount of activity released. We suggest that, in our incubation conditions (up to 3 h), the hormone affects the posttranslational processing of the enzyme. In vivo administration of prazosin blocked the effect of both noradrenaline and fasting on hepatic endothelial lipase activity in whole liver. Those results suggest that catecholamines are involved in the decreased hepatic endothelial lipase activity found in the liver of fasted rats, and points out the role of these hormones in the acute modulation of an enzyme involved in reverse cholesterol transport.

摘要

研究了禁食对成年大鼠肝脏中肝内皮脂肪酶活性的影响。我们发现,无论是雄性还是雌性大鼠,禁食都会使肝内皮脂肪酶活性逐渐降低。重新喂食后,该活性在48小时内恢复到对照值。在来自喂食雄性大鼠的离体肝脏中,添加肝素后灌注液中出现肝内皮脂肪酶活性的急剧峰值。它占组织总活性(肝素释放的 + 残留的)的75%。禁食(24小时)降低了肝素可释放的活性,并且这种作用是整个组织中发现的大部分降低的原因。我们认为这种作用可能是由于肝细胞中该酶的合成和/或分泌减少,因为来自禁食大鼠的离体肝细胞在37℃孵育时,向孵育培养基中释放的活性比来自喂食大鼠的肝细胞少65%。肾上腺素,但不是胰岛素、胰高血糖素、地塞米松、表皮生长因子或T3,降低了从喂食大鼠分离的肝细胞释放的肝内皮脂肪酶活性的量。肾上腺素的作用似乎是由α1受体介导的,因为去氧肾上腺素而非异丙肾上腺素重现了这种作用,并且哌唑嗪而非普萘洛尔阻断了儿茶酚胺的作用。在存在环己酰亚胺的情况下,肾上腺素也降低了释放的活性量。我们认为,在我们的孵育条件下(长达3小时),该激素影响酶的翻译后加工。体内给予哌唑嗪阻断了去甲肾上腺素和禁食对整个肝脏中肝内皮脂肪酶活性的作用。这些结果表明儿茶酚胺参与了禁食大鼠肝脏中肝内皮脂肪酶活性降低的过程,并指出了这些激素在参与逆向胆固醇转运的一种酶的急性调节中的作用。

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