Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

246
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

187
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

2

Information Journal Paper

Title

EVALUATION OF DIABETOGENIC MECHANISM OF HIGH FAT DIET IN COMBINATION WITH ARSENIC EXPOSURE IN MALE MICE

Pages

  164-183

Abstract

 Obesity is a main reason of TYPE 2 DIABETES and also chronic exposure to ARSENIC (As) can produce diabetic symptoms. In previous studies, the association between HIGH-FAT DIET and ARSENIC in the incidence of diabetes was found, but the role of beta cells activity, liver MITOCHONDRIAL OXIDATIVE STRESS, and hepatic enzymes (leptin, adiponectin and beta amylase) was unclear. Thus, present study was conducted to evaluate the diabetogenic mechanism of ARSENIC followed by concomitant administration of HIGH-FAT DIET (HFD) in male mice. In this experimental study, the mice consumed with HFD or low-fat diet (LFD) while exposed to As 25 or 50 ppm in drinking water for 20 weeks. At the end of experiments, hyperglycemia, insulin resistance variables, lipid profile, hepatic enzymes, liver MITOCHONDRIAL OXIDATIVE STRESS, ISLET INSULIN SECRETION, liver, and pancreas histopathology were evaluated in all mice by their own methods. Control HFD fed mice showed a significant increase in FBG, OGTT, HOMA-IR, ITT, lipid profile, leptin, b-amylase, liver MITOCHONDRIAL OXIDATIVE STRESS, hepatic enzymes and decreased FPI, HOMA-b, adiponectin, and ISLET INSULIN SECRETION or content. However, exposure to HFD concomitant with ARSENIC revealed an impressive reduction in FBG, FPI, HOMA-IR, HOMA-b, ITT, lipid profile, and ISLET INSULIN SECRETION or content. This exposure enhanced OGTT, leptin, adiponectin, liver MITOCHONDRIAL OXIDATIVE STRESS, and hepatic enzymes. In conclusion, HFD and ARSENIC concomitant administration induced impairment of OGTT and ISLET INSULIN SECRETION or content through the MITOCHONDRIAL OXIDATIVE STRESS.

Cites

References

  • No record.
  • Cite

    APA: Copy

    AHANGARPOUR, AKRAM, ALBOGHOBEISH, SOHEILA, REZAEI, MOHSEN, KHODAYAR, MOHAMMAD JAVAD, OROOJAN, ALI AKBAR, & ZAINVAND, MARZIEH. (2018). EVALUATION OF DIABETOGENIC MECHANISM OF HIGH FAT DIET IN COMBINATION WITH ARSENIC EXPOSURE IN MALE MICE. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), 17(1), 164-183. SID. https://sid.ir/paper/288866/en

    Vancouver: Copy

    AHANGARPOUR AKRAM, ALBOGHOBEISH SOHEILA, REZAEI MOHSEN, KHODAYAR MOHAMMAD JAVAD, OROOJAN ALI AKBAR, ZAINVAND MARZIEH. EVALUATION OF DIABETOGENIC MECHANISM OF HIGH FAT DIET IN COMBINATION WITH ARSENIC EXPOSURE IN MALE MICE. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR)[Internet]. 2018;17(1):164-183. Available from: https://sid.ir/paper/288866/en

    IEEE: Copy

    AKRAM AHANGARPOUR, SOHEILA ALBOGHOBEISH, MOHSEN REZAEI, MOHAMMAD JAVAD KHODAYAR, ALI AKBAR OROOJAN, and MARZIEH ZAINVAND, “EVALUATION OF DIABETOGENIC MECHANISM OF HIGH FAT DIET IN COMBINATION WITH ARSENIC EXPOSURE IN MALE MICE,” IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), vol. 17, no. 1, pp. 164–183, 2018, [Online]. Available: https://sid.ir/paper/288866/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top