Establishment and Characterization of a Newly Established Diabetic Gerbil Line

PLoS One. 2016 Jul 18;11(7):e0159420. doi: 10.1371/journal.pone.0159420. eCollection 2016.

Abstract

Objectives: We aimed to selectively breed a spontaneous diabetic gerbil when a sub-line of inbred gerbil showed increased blood glucose levels was found recently. Then we investigated the characteristics including the serum insulin, triglyceride, cholesterol, leptin, adiponectin and explored the underlying molecular mechanism for the diabetic phenotype.

Methods: The spontaneous diabetic line of gerbils was selectively inbreed the sub-line of gerbil by monitoring blood glucose of each animal. The serum insulin, adiponectin, and leptin levels were tested using an ELISA kit. The expression levels of GLUT4, Akt, leptin, adiponectin, and calpain 10 (CAPN10) were tested by western blot and Quantitative Real-time PCR (qPCR) in liver, skeletal muscle, and white adipose.

Results: Our results show that the percentages of animals with FPG≥5.2 (mmol/l), PG2h≥6.8 (mmol/l) and both FPG≥5.2 and PG2h≥6.8 (mmol/l) were increased with the number of breeding generations from F0 (21.33%) to F6 (38.46%). These diabetic gerbils exhibited insulin resistance and leptin resistance as well as decreased adiponectin level in the serum. We also observed decreased expression of adiponectin and increased expression of leptin in the skeletal muscle, respectively.

Conclusions: These results indicate that we have primarily established a spontaneous diabetic gerbil line, and the diabetic phenotypes may have been accounted for by altered expression of leptin and adiponectin.

MeSH terms

  • Adiponectin / genetics*
  • Adiponectin / metabolism
  • Adipose Tissue, White / metabolism
  • Adipose Tissue, White / pathology
  • Animals
  • Blood Glucose / metabolism
  • Breeding
  • Calpain / genetics
  • Calpain / metabolism
  • Cholesterol / blood
  • Diabetes Mellitus / genetics*
  • Diabetes Mellitus / metabolism
  • Diabetes Mellitus / pathology
  • Diabetes Mellitus / veterinary*
  • Female
  • Founder Effect*
  • Gene Expression Regulation
  • Gerbillinae / genetics
  • Gerbillinae / metabolism*
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Insulin / blood
  • Insulin Resistance
  • Leptin / genetics*
  • Leptin / metabolism
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Phenotype
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Triglycerides / blood

Substances

  • Adiponectin
  • Blood Glucose
  • Glucose Transporter Type 4
  • Insulin
  • Leptin
  • Triglycerides
  • Cholesterol
  • Proto-Oncogene Proteins c-akt
  • Calpain
  • calpain 10

Grants and funding

This study was funded by the National Science Foundation of China Nos. 31272393 and 31572341 Xiaoyan Du, the website is http://www.nsfc.gov.cn/Portal0/default152.htm, Key Projects in the National Science & Technology Pillar Program (No. 2015BAI09B01) and the Beijing Natural Science Foundation (No. 7141002), the website is http://www.bjnsf.org.