4.6 Article

Single and combined effect of bisphenol A with high sucrose diet on the diabetic and renal tubular dysfunction phenotypes in Drosophila melanogaster

期刊

出版社

ELSEVIER
DOI: 10.1016/j.etap.2022.103977

关键词

Bisphenol A; High sucrose diet; Type 2 diabetes; Drosophila; Malpighian tubules

资金

  1. UGC SRF [22/06/2014 (i) EU-V]
  2. CSIR-SRF [31/29(0291)/2018-EMR-I]
  3. Council of Scientific and Industrial Research (CSIR), New Delhi
  4. DST [DST/INSPIRE/04/2015/001777, EEQ/2020/000586]

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This study investigates the effects of bisphenol A (BPA) exposure and combined exposure of BPA + HSD on glucose homeostasis and renal complications in Drosophila. The results show that exposure to 1.0 mM BPA alone induces type 2 diabetes-like condition in adult male Drosophila, while combined exposure of BPA + HSD aggravates the severity of diabetes and renal tubular dysfunction. This study suggests the use of Drosophila model to study environmental chemical-induced diabetes-mediated renal dysfunction.
In the present study, effect of exposure of bisphenol A (BPA) and combined exposure of BPA + HSD has been investigated on the glucose homeostasis and associated renal complications in Drosophila. Exposure of 1.0 mM BPA alone induced type 2 diabetes like condition (T2D) in adult male D. melanogaster via oxidative stress. Elevated TGF-beta signaling was evident by increased expression of baboon (babo) in BPA exposed organism that stimulated the modulation of extracellular matrix (ECM) component collagen IV resulting in the fibrosis of the Malpighian tubules (MTs). Combined exposure of BPA + HSD (high sucrose diet) resulted in the increased magnitude of T2D and MTs dysfunction parameters. Taken together, the study illustrates that BPA has diabetogenic potential in exposed Drosophila that caused adverse effects on their MTs and combined exposure with BPA and HSD could aggravate the renal tubular dysfunction. The study further suggests the use of Drosophila model to study the environmental chemicals induced diabetes mediated renal dysfunction.

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