Department of Endocrinology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Mol Cell Endocrinol. 2011 Apr 30;337(1-2):101-13. doi: 10.1016/j.mce.2011.02.002. Epub 2011 Feb 23.
Poorly controlled type1 diabetes is associated with hormonal imbalances and increased cell death in different tissues, including the pituitary, hypothalamus and cerebellum. In the pituitary, lactotrophs are the cell population with the greatest increase in cell death, whereas in the hypothalamus and cerebellum astrocytes are most highly affected. Insulin treatment can delay, but does not prevent, diabetic complications. As ghrelin and growth hormone (GH) secretagogues are reported to prevent apoptosis in different tissues, and to modulate glucose homeostasis, a combined hormonal treatment may be beneficial. Hence, we analyzed the effect of insulin and GH-releasing peptide 6 (GHRP-6) on diabetes-induced apoptosis in the pituitary, hypothalamus and cerebellum of diabetic rats. Adult male Wistar rats were made diabetic by streptozotocin injection (65 mg/kg ip) and divided into four groups from diabetes onset: those receiving a daily sc injection of saline (1 ml/kg/day), GHRP-6 (150 μg/kg/day), insulin (1-8U/day) or insulin plus GHRP-6 for 8 weeks. Control non-diabetic rats received saline (1 ml/kg/day). Diabetes increased cell death in the pituitary, hypothalamus and cerebellum (P<0.05). In the pituitary, insulin treatment prevented diabetes-induced apoptosis (P<0.01), as well as the decline in prolactin and GH mRNA levels (P<0.05). In the hypothalamus, neither insulin nor GHRP-6 decreased diabetes-induced cell death. However, the combined treatment of insulin+GHRP-6 prevented the diabetes induced-decrease in glial fibrillary acidic protein (GFAP) levels (P<0.05). In the cerebellum, although insulin treatment increased GFAP levels (P<0.01), only the combined treatment of insulin+ GHRP-6 decreased diabetes-induced apoptosis (P<0.05). In conclusion, insulin and GHRP-6 exert tissue specific effects in STZ-diabetic rats and act synergistically on some processes. Indeed, insulin treatment does not seem to be effective on preventing some of the diabetes-induced alterations in the central nervous system.
1 型糖尿病控制不佳与激素失衡和不同组织中的细胞死亡增加有关,包括垂体、下丘脑和小脑。在垂体中,催乳素细胞是细胞死亡增加最多的细胞群体,而在下丘脑和小脑,星形胶质细胞受影响最大。胰岛素治疗可以延迟,但不能预防糖尿病并发症。由于生长激素释放肽 6(GHRP-6)和生长激素促分泌素被报道可以防止不同组织中的细胞凋亡,并调节葡萄糖稳态,因此联合激素治疗可能是有益的。因此,我们分析了胰岛素和 GHRP-6 对糖尿病大鼠垂体、下丘脑和小脑中糖尿病诱导的细胞凋亡的影响。成年雄性 Wistar 大鼠通过链脲佐菌素注射(65mg/kg ip)制成糖尿病,并从糖尿病发病开始分为四组:每天接受 1ml/kg 生理盐水(1ml/kg/day)、GHRP-6(150μg/kg/day)、胰岛素(1-8U/day)或胰岛素加 GHRP-6 注射 8 周。对照非糖尿病大鼠接受生理盐水(1ml/kg/day)。糖尿病增加了垂体、下丘脑和小脑的细胞死亡(P<0.05)。在垂体中,胰岛素治疗可预防糖尿病诱导的细胞凋亡(P<0.01),并可降低催乳素和 GH mRNA 水平(P<0.05)。在下丘脑,胰岛素和 GHRP-6 均不能降低糖尿病诱导的细胞死亡。然而,胰岛素+GHRP-6 的联合治疗可预防糖尿病诱导的神经胶质纤维酸性蛋白(GFAP)水平下降(P<0.05)。在小脑,尽管胰岛素治疗增加了 GFAP 水平(P<0.01),但只有胰岛素+GHRP-6 的联合治疗可降低糖尿病诱导的细胞凋亡(P<0.05)。总之,胰岛素和 GHRP-6 在 STZ 糖尿病大鼠中具有组织特异性作用,并在某些过程中协同作用。事实上,胰岛素治疗似乎对预防中枢神经系统中一些由糖尿病引起的改变无效。