Literature DB >> 21352888

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.

Miriam Granado1, Cristina García-Cáceres, María Tuda, Laura M Frago, Julie A Chowen, Jesús Argente.   

Abstract

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.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21352888     DOI: 10.1016/j.mce.2011.02.002

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  5 in total

1.  Neuroprotective actions of ghrelin and growth hormone secretagogues.

Authors:  Laura M Frago; Eva Baquedano; Jesús Argente; Julie A Chowen
Journal:  Front Mol Neurosci       Date:  2011-09-28       Impact factor: 5.639

Review 2.  A proteomic approach to obesity and type 2 diabetes.

Authors:  Elena López-Villar; Gabriel Á Martos-Moreno; Julie A Chowen; Shigeru Okada; John J Kopchick; Jesús Argente
Journal:  J Cell Mol Med       Date:  2015-05-09       Impact factor: 5.310

3.  Growth hormone-releasing peptide-biotin conjugate stimulates myocytes differentiation through insulin-like growth factor-1 and collagen type I.

Authors:  Chae Jin Lim; Jung Eun Jeon; Se Kyoo Jeong; Seok Jeong Yoon; Seon Deok Kwon; Jina Lim; Keedon Park; Dae Yong Kim; Jeong Keun Ahn; Bong-Woo Kim
Journal:  BMB Rep       Date:  2015-09       Impact factor: 4.778

4.  Neural stem cells in the diabetic brain.

Authors:  Tomás P Bachor; Angela M Suburo
Journal:  Stem Cells Int       Date:  2012-11-14       Impact factor: 5.443

5.  Stimulation of autophagy promotes functional recovery in diabetic rats with spinal cord injury.

Authors:  Kai-liang Zhou; Yi-fei Zhou; Kai Wu; Nai-feng Tian; Yao-sen Wu; Yong-li Wang; De-heng Chen; Bin Zhou; Xiang-yang Wang; Hua-zi Xu; Xiao-lei Zhang
Journal:  Sci Rep       Date:  2015-11-24       Impact factor: 4.379

  5 in total

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