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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.
- Source :
-
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2011 Apr 30; Vol. 337 (1-2), pp. 101-13. Date of Electronic Publication: 2011 Feb 23. - Publication Year :
- 2011
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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.<br /> (Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.)
- Subjects :
- Animals
Caspases metabolism
Cerebellum metabolism
Diabetes Mellitus, Experimental chemically induced
Diabetes Mellitus, Experimental metabolism
Glial Fibrillary Acidic Protein metabolism
HSP72 Heat-Shock Proteins metabolism
Hypothalamus metabolism
Insulin-Like Growth Factor I genetics
Insulin-Like Growth Factor I metabolism
Male
Pituitary Gland metabolism
Pituitary Hormones genetics
Pituitary Hormones metabolism
Proliferating Cell Nuclear Antigen metabolism
Proto-Oncogene Proteins c-bcl-2 metabolism
Rats
Rats, Wistar
Receptor, Insulin genetics
Receptor, Insulin metabolism
Receptors, Ghrelin genetics
Receptors, Ghrelin metabolism
Streptozocin
Transcription, Genetic drug effects
Tumor Necrosis Factor-alpha metabolism
Weight Gain drug effects
X-Linked Inhibitor of Apoptosis Protein metabolism
Cell Death drug effects
Cerebellum pathology
Diabetes Mellitus, Experimental pathology
Hypothalamus pathology
Insulin pharmacology
Oligopeptides pharmacology
Pituitary Gland pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8057
- Volume :
- 337
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Molecular and cellular endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 21352888
- Full Text :
- https://doi.org/10.1016/j.mce.2011.02.002