Fain J N, Bahouth S W
Department of Biochemistry, College of Medicine, University of Tennessee at Memphis, 38163, USA.
Biochem Pharmacol. 1998 Apr 15;55(8):1309-14. doi: 10.1016/s0006-2952(97)00638-2.
A greater understanding of the factors causing the enhanced release of leptin by adipocytes in obesity is needed. Experiments were designed to determine the effects of actinomycin D on leptin release by isolated rat adipocytes during primary culture for 24 hr. In adipocytes from fed hypothyroid rats, the initial rate of leptin release over the first 6 hr was not maintained over the next 18 hr. The decline in leptin release by adipocytes in primary culture between 6 and 24 hr was reduced markedly by either dexamethasone or actinomycin D. Both actinomycin D and dexamethasone also reduced the loss of leptin mRNA seen over the 24-hr incubation. Maximal effects on leptin release and leptin mRNA accumulation required only 0.1 microM of actinomycin D, a concentration that had no significant effect on the 18S RNA content of adipocytes at the end of a 24-hr incubation. In contrast to the reduced loss of leptin mRNA seen at 24 hr, the loss of glyceraldehyde-3-phosphate dehydrogenase messenger ribonucleic acid (GAPDH mRNA) was enhanced in the presence of 0.1 microM of actinomycin D. The effects of dexamethasone could be differentiated from those of actinomycin D by the finding that cycloheximide blocked the reduced loss of leptin mRNA due to dexamethasone while having no effect on that due to actinomycin D. These results point to a unique regulation of leptin release and leptin mRNA levels by actinomycin D.
我们需要更深入地了解导致肥胖时脂肪细胞中瘦素释放增加的因素。本实验旨在确定放线菌素D对原代培养24小时的离体大鼠脂肪细胞瘦素释放的影响。在喂食的甲状腺功能减退大鼠的脂肪细胞中,最初6小时的瘦素释放初始速率在接下来的18小时内未维持。地塞米松或放线菌素D均可显著降低原代培养的脂肪细胞在6至24小时之间瘦素释放的下降。放线菌素D和地塞米松还减少了24小时孵育期间观察到的瘦素mRNA的损失。对瘦素释放和瘦素mRNA积累的最大影响仅需要0.1微摩尔的放线菌素D,这一浓度在24小时孵育结束时对脂肪细胞的18S RNA含量没有显著影响。与24小时时瘦素mRNA损失减少相反,在存在0.1微摩尔放线菌素D的情况下,甘油醛-3-磷酸脱氢酶信使核糖核酸(GAPDH mRNA)的损失增加。通过发现环己酰亚胺阻断了地塞米松导致的瘦素mRNA损失减少,而对放线菌素D导致的损失没有影响,可将地塞米松的作用与放线菌素D的作用区分开来。这些结果表明放线菌素D对瘦素释放和瘦素mRNA水平具有独特的调节作用。