Stace P B, Fatania H R, Jackson A, Kerbey A L, Randle P J
Nuffield Department of Clinical Biochemistry, University of Oxford, John Radcliffe Hospital, UK.
Biochim Biophys Acta. 1992 Jun 10;1135(2):201-6. doi: 10.1016/0167-4889(92)90137-z.
Starvation increased pyruvate dehydrogenase (PDH) kinase activity in extracts of freshly excised rat soleus 2.2-fold (from 0.6 min-1 in fed rats to 1.31 min-1 in 48-h-starved rats). In fed rats, activities were unchanged following 24 h of culture in medium 199, but increased 2.1-fold on 24 h of culture with 50 microM dibutyryl cAMP plus 1 mM n-octanoate and 1.6-1.7-fold with either agent alone. Approx. 70% of the increase in PDH kinase induced by starvation was lost following 24 h of culture in medium 199; the loss was prevented by 50 microM dibutyryl cAMP plus 1 mM n-octanoate. cAMP concentrations in fresh soleus muscle were 1 nmol/g (fed rats) and 1.6 nmol/g (starved rats). After 20-60 min of culture the fed-starved difference disappeared and [cAMP] fell to 0.4 nmol/g. Calcitonin-gene-related peptide (CGRP) increased cAMP 3-fold; the increase was maintained throughout 24 h of culture, but was readily reversed at 30 min or 24 h of culture by 60-min incubation with CGRP-free medium. Starvation of the rat (48 h) had no effect on the sensitivity of soleus towards the [cAMP]-increasing effect of CGRP. It is concluded that culture may reverse effects of starvation on PDH kinase activity by lowering cAMP and by removal from the in vivo effects of circulating free fatty acids; and that starvation and CGRP had no detectable long-term effects on the cAMP system in soleus muscle.
饥饿使新鲜切除的大鼠比目鱼肌提取物中的丙酮酸脱氢酶(PDH)激酶活性增加了2.2倍(从喂食大鼠的0.6分钟-1增加到饥饿48小时大鼠的1.31分钟-1)。在喂食大鼠中,在199培养基中培养24小时后活性没有变化,但在含有50 microM二丁酰环磷腺苷(dibutyryl cAMP)加1 mM正辛酸的培养基中培养24小时后增加了2.1倍,单独使用任何一种试剂时增加了1.6 - 1.7倍。在199培养基中培养24小时后,饥饿诱导的PDH激酶增加量约70%消失;50 microM二丁酰环磷腺苷加1 mM正辛酸可防止这种损失。新鲜比目鱼肌中的环磷腺苷(cAMP)浓度为1 nmol/g(喂食大鼠)和1.6 nmol/g(饥饿大鼠)。培养20 - 60分钟后,喂食与饥饿的差异消失,[cAMP]降至0.4 nmol/g。降钙素基因相关肽(CGRP)使cAMP增加3倍;这种增加在整个24小时培养过程中保持,但在培养30分钟或24小时时,通过在无CGRP培养基中孵育60分钟可迅速逆转。大鼠饥饿(48小时)对比目鱼肌对CGRP增加[cAMP]作用的敏感性没有影响。结论是,培养可能通过降低cAMP以及消除循环游离脂肪酸的体内效应来逆转饥饿对PDH激酶活性的影响;并且饥饿和CGRP对比目鱼肌中的cAMP系统没有可检测到的长期影响。