Charon C, Krief S, Diot-Dupuy F, Strosberg A D, Emorine L J, Bazin R
INSERM U 177, Paris, France.
Biochem J. 1995 Dec 15;312 ( Pt 3)(Pt 3):781-8. doi: 10.1042/bj3120781.
This study was undertaken to determine whether receptor and non-receptor components of the adenylate cyclase (AC) cascade were altered in brown adipose tissue (BAT) of 14-day-old pre-obese (fa/fa) rats, before endocrine status is strongly modified by fa gene expression. Activity of the AC catalytic subunit did not differ between the two genotypes. In fa/fa rats compared with control Fa/fa rats, there was a 50% decrease in the activity of alpha Gs (stimulated by NaF or guanosine 5'-[gamma-thio]triphosphate) but no change in protein content (Western blotting). alpha Gi function, assessed by the inhibitory action of low concentrations of guanosine 5'-[beta gamma-imido]triphosphate upon 10(-4) M forskolin-stimulated AC activity, was equally low in both genotypes. Analysis of dose-response curves for different beta-agonists revealed that (i) both the basal and the maximally stimulated activity of AC were 2-fold lower in fa/fa rats than in Fa/fa rats; (ii) BRL37344 and CGP12177 (beta 3 agonists) were less potent in fa/fa than in Fa/fa rats (Kact. multiplied by 2); (iii) noradrenaline and isoprenaline (Iso), at the low-affinity site (beta 3-AR), were less potent in fa/fa than in Fa/fa pups (Kact. increased by 30 and 20% respectively). At the high-affinity site (mainly beta 1) these two agonists were more potent in fa/fa than in Fa/fa rats (Kact. decreased by 40 and 80% respectively). In good agreement with the latter result, the beta 1-adrenergic receptor (beta 1-AR)-selective antagonist CGP20712A had more effect on the Iso-stimulated AC activity in pre-obese than in lean pups (2-fold decreased in IC50). Binding experiments with [3H]CGP12177 show that in BAT of suckling rats, beta 3-ARs represent 80% of the total beta-ARs. Bmax values for the two sites were not affected by the genotype, although the beta 3-AR mRNA concentration in BAT (quantitative reverse-transcriptase PCR) was 3-fold lower in fa/fa rats than in Fa/fa pups. In conclusion, these results provide evidence for alterations in beta 1- and beta 3-AR signalling in BAT of 14-day-old suckling pre-obese Zucker rats with a decreased activity of alpha Gs. The impaired AC responsiveness to catecholamines might be a primary contributor to the development of this genetic obesity.
本研究旨在确定在14日龄肥胖前期(fa/fa)大鼠的棕色脂肪组织(BAT)中,腺苷酸环化酶(AC)级联反应的受体和非受体成分是否发生改变,此时fa基因表达尚未强烈改变内分泌状态。两种基因型大鼠的AC催化亚基活性无差异。与对照Fa/fa大鼠相比,fa/fa大鼠中αGs(由氟化钠或鸟苷5'-[γ-硫代]三磷酸刺激)的活性降低了50%,但蛋白质含量(蛋白质印迹法)无变化。通过低浓度鸟苷5'-[βγ-亚氨基]三磷酸对10^(-4)M福斯可林刺激的AC活性的抑制作用评估αGi功能,两种基因型大鼠的该功能同样较低。对不同β-激动剂的剂量反应曲线分析表明:(i)fa/fa大鼠中AC的基础活性和最大刺激活性均比Fa/fa大鼠低2倍;(ii)BRL37344和CGP12177(β3激动剂)在fa/fa大鼠中的效力低于Fa/fa大鼠(Kact乘以2);(iii)去甲肾上腺素和异丙肾上腺素(Iso)在低亲和力位点(β3-AR),在fa/fa大鼠中的效力低于Fa/fa幼崽(Kact分别增加30%和20%)。在高亲和力位点(主要是β1),这两种激动剂在fa/fa大鼠中的效力高于Fa/fa大鼠(Kact分别降低40%和80%)。与后一结果高度一致,β1-肾上腺素能受体(β1-AR)选择性拮抗剂CGP20712A对肥胖前期幼崽中Iso刺激的AC活性的影响比对瘦幼崽的影响更大(IC50降低2倍)。用[3H]CGP12177进行的结合实验表明,在哺乳期大鼠的BAT中,β3-ARs占总β-ARs的80%。尽管fa/fa大鼠BAT中β3-AR mRNA浓度(定量逆转录酶PCR)比Fa/fa幼崽低3倍,但两个位点的Bmax值不受基因型影响。总之,这些结果证明14日龄哺乳期肥胖前期 Zucker大鼠的BAT中β1-和β3-AR信号传导发生改变,αGs活性降低。AC对儿茶酚胺反应性受损可能是这种遗传性肥胖发生的主要原因。