首页> 外文期刊>Molecular and Cellular Endocrinology >Insulin and growth hormone-releasing peptide-6 (GHRP-6) have differential beneficial effects on cell turnover in the pituitary, hypothalamus and cerebellum of streptozotocin (STZ)-induced diabetic rats.
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Insulin and growth hormone-releasing peptide-6 (GHRP-6) have differential beneficial effects on cell turnover in the pituitary, hypothalamus and cerebellum of streptozotocin (STZ)-induced diabetic rats.

机译:胰岛素和生长激素释放肽6(GHRP-6)对链脲佐菌素(STZ)诱导的糖尿病大鼠垂体,下丘脑和小脑的细胞更新具有不同的有益作用。

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摘要

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 mug/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.
机译:不良控制的1型糖尿病与荷尔蒙失调和包括垂体,下丘脑和小脑在内的不同组织中细胞死亡的增加有关。在垂体中,营养缺陷型是细胞死亡增加最大的细胞群,而在下丘脑和小脑星形胶质细胞受到的影响最大。胰岛素治疗可以延迟但不能预防糖尿病并发症。由于据报道生长素释放肽和生长激素(GH)促分泌素可防止不同组织的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GH释放肽6(GHRP-6)对糖尿病诱导的糖尿病大鼠垂体,下丘脑和小脑细胞凋亡的影响。成年雄性Wistar大鼠通过链脲佐菌素注射(65 mg / kg ip)制成糖尿病,从糖尿病发作开始分为四组:每天皮下注射生理盐水(1 ml / kg /天),GHRP-6(150杯/公斤/天),胰岛素(1-8U /天)或胰岛素加GHRP-6,共8周。对照组非糖尿病大鼠接受盐水(1 ml / kg /天)。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引起的细胞凋亡(P <0.01)以及催乳素和GH mRNA水平的下降(P <0.05)。在下丘脑中,胰岛素和GHRP-6均不能减少糖尿病引起的细胞死亡。然而,胰岛素+ GHRP-6的联合治疗可预防糖尿病引起的胶质纤维酸性蛋白(GFAP)水平降低(P <0.05)。在小脑中,尽管胰岛素治疗可增加GFAP水平(P <0.01),但只有胰岛素+ GHRP-6的联合治疗才能降低糖尿病引起的细胞凋亡(P <0.05)。总之,胰岛素和GHRP-6在STZ糖尿病大鼠中发挥组织特异性作用,并在某些过程中协同作用。实际上,胰岛素治疗似乎并不能有效预防糖尿病引起的中枢神经系统改变。

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