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脂肪组织中的清除因子脂肪酶。嘌呤霉素和放线菌素的研究。

Clearing-factor lipase in adipose tissue. Studies with puromycin and actinomycin.

作者信息

Wing D R, Robinson D S

出版信息

Biochem J. 1968 Feb;106(3):667-76. doi: 10.1042/bj1060667.

Abstract
  1. When adipose tissue from starved rats is incubated in a medium containing glucose, insulin, heparin and actinomycin (5mug./ml.) the total clearing-factor lipase activity of the system increases at least tenfold over a period of 9hr. In the absence of actinomycin, enzyme activity also increases, but to a lesser extent and for only about 3hr. Some enzyme activity appears in the incubation medium in both the presence and the absence of actinomycin. 2. When the glucose and insulin of the incubation medium are replaced by pyruvate and heparin is omitted, an increase in the total clearing-factor lipase activity in the presence of actinomycin still occurs, but only after a lag of several hours. When only heparin is omitted from the medium, the rise in enzyme activity begins immediately, but there is a shoulder in the time-course curve after a few hours. In the absence of heparin, little enzyme activity appears in the incubation medium. 3. The increases in enzyme activity in the presence of actinomycin are prevented if puromycin (0.5mg./ml.) is present in the incubation medium. 4. Catecholamines and corticotrophin inhibit the increase in enzyme activity caused by actinomycin. 5. The clearing-factor lipase activity of adipose tissue from fed animals declines with a half-life of between 1 and 1.5hr. when the tissue is incubated in the presence of puromycin. The clearing-factor lipase activity of adipose tissue from starved animals is stable under similar circumstances, as is the raised activity found after such tissue has been incubated in the presence of actinomycin. 6. Clearing-factor lipase extracted from adipose tissue of fed animals is less stable in solution than that extracted from the tissue of starved animals after this has been incubated in the presence of actinomycin.
摘要
  1. 将饥饿大鼠的脂肪组织在含有葡萄糖、胰岛素、肝素和放线菌素(5微克/毫升)的培养基中孵育时,该系统的总清除因子脂肪酶活性在9小时内至少增加10倍。在没有放线菌素的情况下,酶活性也会增加,但增加幅度较小,且仅持续约3小时。无论有无放线菌素,孵育培养基中都会出现一些酶活性。2. 当孵育培养基中的葡萄糖和胰岛素被丙酮酸取代且省略肝素时,在有放线菌素存在的情况下,总清除因子脂肪酶活性仍会增加,但会有几个小时的延迟。当仅从培养基中省略肝素时,酶活性立即开始上升,但几小时后时间进程曲线会出现一个平台期。在没有肝素的情况下,孵育培养基中几乎没有酶活性出现。3. 如果孵育培养基中存在嘌呤霉素(0.5毫克/毫升),则会阻止放线菌素存在时酶活性的增加。4. 儿茶酚胺和促肾上腺皮质激素会抑制放线菌素引起的酶活性增加。5. 当在嘌呤霉素存在的情况下孵育时,喂食动物的脂肪组织的清除因子脂肪酶活性以1至1.5小时的半衰期下降。饥饿动物的脂肪组织的清除因子脂肪酶活性在类似情况下是稳定的,在放线菌素存在下孵育后的升高活性也是如此。6. 从喂食动物的脂肪组织中提取的清除因子脂肪酶在溶液中的稳定性低于从饥饿动物的脂肪组织中提取的清除因子脂肪酶,后者在放线菌素存在下孵育后。

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