Department of Bio-Medical Sciences Catania, Italy.
Peptides. 2012 Sep;37(1):32-9. doi: 10.1016/j.peptides.2012.06.004. Epub 2012 Jun 18.
The retinal expression and distribution of pituitary adenylate cyclase-activating peptide (PACAP) and vasoactive intestinal peptide (VIP) and their receptors was investigated in early streptozotocin (STZ)-induced diabetic rats. Diabetes was induced in rats by STZ injection (60 mg/kg i.p.). PACAP, VIP and their receptors in nondiabetic control and diabetic retinas were assayed by quantitative real-time PCR and Western blot 1 and 3 weeks after STZ injection. Effects of intravitreal treatment with PACAP38 on the expression of the two apoptotic-related genes Bcl-2 and p53 were also evaluated. PACAP and VIP, as well as VPAC1 and VPAC2 receptors, but not PAC1 mRNA levels, were transiently induced in retinas 1 week following STZ. These findings were confirmed by immunoblot analyses. Three weeks after the induction of diabetes, significant decreases in the expression of peptides and their receptors were observed, Bcl-2 expression decreased and p53 expression increased. Intravitreal injection of PACAP38 restored STZ-induced changes in retinal Bcl-2 and p53 expression to nondiabetic levels. The initial upregulation of PACAP, VIP and related receptors and the subsequent downregulation in retina of diabetic rats along with the protective effects of PACAP38 treatment, suggest a role for both peptides in the pathogenesis of diabetic retinopathy.
研究了垂体腺苷酸环化酶激活肽(PACAP)和血管活性肠肽(VIP)及其受体在早期链脲佐菌素(STZ)诱导的糖尿病大鼠中的视网膜表达和分布。大鼠通过 STZ 注射(60mg/kg ip)诱导糖尿病。在 STZ 注射后 1 周和 3 周,通过定量实时 PCR 和 Western blot 测定非糖尿病对照和糖尿病视网膜中的 PACAP、VIP 和它们的受体。还评估了 PACAP38 对两种与凋亡相关基因 Bcl-2 和 p53 的表达的影响。PACAP 和 VIP 以及 VPAC1 和 VPAC2 受体,但不是 PAC1 mRNA 水平,在 STZ 后 1 周短暂诱导。免疫印迹分析证实了这一发现。糖尿病诱导 3 周后,观察到肽及其受体的表达显著下降,Bcl-2 表达下降,p53 表达增加。PACAP38 的玻璃体内注射将 STZ 诱导的视网膜 Bcl-2 和 p53 表达的变化恢复到非糖尿病水平。糖尿病大鼠视网膜中 PACAP、VIP 和相关受体的初始上调以及随后的下调以及 PACAP38 治疗的保护作用表明,这两种肽在糖尿病性视网膜病变的发病机制中起作用。