Suppressing hyperinsulinemia prevents obesity but causes rapid onset of diabetes in leptin-deficient Lepob/ob mice
| Autor: | Susanne M. Clee, Anna M. D'souza, Timothy J. Kieffer, James D. Johnson |
|---|---|
| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
medicine.medical_specialty endocrine system lcsh:Internal medicine endocrine system diseases medicine.medical_treatment education 030209 endocrinology & metabolism 03 medical and health sciences 0302 clinical medicine Diabetes mellitus Internal medicine medicine Hyperinsulinemia Glucose homeostasis lcsh:RC31-1245 Molecular Biology health care economics and organizations 2. Zero hunger geography geography.geographical_feature_category Chemistry Insulin Leptin nutritional and metabolic diseases Cell Biology medicine.disease Islet Obesity 030104 developmental biology Endocrinology hormones hormone substitutes and hormone antagonists Hormone |
| Zdroj: | Molecular Metabolism, Vol 5, Iss 11, Pp 1103-1112 (2016) |
| ISSN: | 2212-8778 |
| DOI: | 10.1016/j.molmet.2016.09.007 |
| Popis: | Objective: Hyperinsulinemia is commonly associated with obesity. Mice deficient in the adipose-derived hormone leptin (Lepob/ob) develop hyperinsulinemia prior to onset of obesity and glucose intolerance. Whether the excess of circulating insulin is a major contributor to obesity and impaired glucose homeostasis in Lepob/ob mice is unclear. It has been reported previously that diet-induced obesity in mice can be prevented by reducing insulin gene dosage. In the present study, we examined the effects of genetic insulin reduction in Lepob/ob mice on circulating insulin, body composition, and glucose homeostasis. Methods: Leptin expressing (Lepwt/wt) mice lacking 3 insulin alleles were crossed with Lepob/ob mice to generate Lepob/ob and Lepwt/wt littermates lacking 1 (Ins1+/+;Ins2+/−), 2 (Ins1+/+;Ins2−/−) or 3 (Ins1+/−;Ins2−/−) insulin alleles. Animals were assessed for body weight gain, body composition, glucose homeostasis, and islet morphology. Results: We found that in young Lepob/ob mice, loss of 2 or 3 insulin alleles reduced plasma insulin levels by 75–95% and attenuated body weight gain by 50–90% compared to Ins1+/+;Ins2+/−;Lepob/ob mice. This corresponded with ∼30% and ∼50% reduced total body fat in Ins1+/+;Ins2−/−;Lepob/ob and Ins1+/−;Ins2−/−;Lepob/ob mice, respectively. Loss of 2 or 3 insulin alleles in young Lepob/ob mice resulted in onset of fasting hyperglycemia by 4 weeks of age, exacerbated glucose intolerance, and abnormal islet morphology. In contrast, loss of 1,2 or 3 insulin alleles in Lepwt/wt mice did not significantly alter plasma insulin levels, body weight, fat mass, fasting glycemia, or glucose tolerance. Conclusion: Taken together, our findings indicate that hyperinsulinemia is required for excess adiposity in Lepob/ob mice and sufficient insulin production is necessary to maintain euglycemia in the absence of leptin. Author Video: Author Video Watch what authors say about their articles Keywords: Hyperinsulinemia, Lepob/ob, Obesity, Hyperglycemia |
| Databáze: | OpenAIRE |
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