Derkach K V, Chistyakova O V, Shpakov A O
Zh Evol Biokhim Fiziol. 2014 Mar-Apr;50(2):85-91.
One of the key causes of diabetes mellitus (DM) and its complications are hormonal disturbances in functioning of hormonal signaling systems, including the adenylyl cyclase signaling system (ACSS). The goal of this work was to study the functional state and hormonal sensitivity of ACSS in the epididymal adipose tissue of male rats in the 7-month model of mild type 1 DM (DM1), in the 18-month neonatal model of type 2 DM (DM2), and in the taken for comparison model of the 30-day acute DM1. It is shown for the first time that in adipocytes from the epididymal fat of rats with the studied DM models the basal AC activity and its stimulation by forskolin were decreased, which indicates a weakening of the catalytic function of the enzyme adenylyl cyclase (AC). Stimulation of AC by guanine nucleotides in DM changed to the lesser extent, which speaks in favor of preservation of functions of heterotrimeric G(s)-proteins in the epididymal fat. In rats with DM1 the sensitivity of AC of adipocytes to agonists of β-adrenergic receptors (β-AR), activators of lipolysis, remained practically unchanged, while in animals with DM2 the AC stimulating effects of β-AR-agonists were reduced or completely blocked, like in the case of β3-AR-agonist BRL-37344 and CL-316243. In adipocytes of rats with DM1 the AC inhibitory effect of N6-cyclopentyladenosine, agonist of type 1 adenosine receptors (Aden1R), an inhibitor of lipolysis, was attenuated, whe- reas in DM2 this effect was completely preserved. Thus, in the epididymal adipose tissue of rats with DM1 the antilipolytic AC cascades including Aden1R were decreased and the stimulation of AC by β-AR-agonists was preserved, whereas in rats with DM2 the β-AR-mediated AC cascades activating lipolysis were reduced, but Aden1R-mediated AC cascades inhibiting lipolysis did not change. The changes of hormonal regulation of ACSS in adipocytes from the epididymal fat lead to disturbances of the metabolic status of animal with DM1 and DM2 and should be considered in the diagnostics and treatment of DM and its complications.
糖尿病(DM)及其并发症的关键病因之一是激素信号系统功能中的激素紊乱,包括腺苷酸环化酶信号系统(ACSS)。本研究的目的是在7个月的轻度1型糖尿病(DM1)模型、18个月的2型糖尿病(DM2)新生儿模型以及用于比较的30天急性DM1模型中,研究雄性大鼠附睾脂肪组织中ACSS的功能状态和激素敏感性。首次表明,在患有上述糖尿病模型的大鼠附睾脂肪中的脂肪细胞中,基础AC活性及其受福司可林的刺激作用降低,这表明腺苷酸环化酶(AC)的催化功能减弱。糖尿病中鸟嘌呤核苷酸对AC的刺激作用变化较小,这表明附睾脂肪中异源三聚体G(s)蛋白的功能得以保留。在患有DM1的大鼠中,脂肪细胞的AC对β-肾上腺素能受体(β-AR)激动剂(脂解激活剂)的敏感性基本保持不变,而在患有DM2的动物中,β-AR激动剂对AC的刺激作用降低或完全被阻断,如β3-AR激动剂BRL-37344和CL-316243的情况。在患有DM1的大鼠脂肪细胞中,N6-环戊基腺苷(1型腺苷受体(Aden1R)激动剂,脂解抑制剂)对AC的抑制作用减弱,而在DM2中这种作用完全保留。因此,在患有DM1的大鼠附睾脂肪组织中,包括Aden1R在内的抗脂解AC级联反应减弱,而β-AR激动剂对AC的刺激作用得以保留,而在患有DM2的大鼠中,β-AR介导的激活脂解的AC级联反应减弱,但Aden1R介导的抑制脂解的AC级联反应未改变。附睾脂肪中脂肪细胞ACSS激素调节的变化导致患有DM1和DM2的动物代谢状态紊乱,在糖尿病及其并发症的诊断和治疗中应予以考虑。