Biochemical Profiling of Arsenic Trioxide-Induced Impaired Carbohydrate Metabolism and its Therapeutic Intervention via Modulation of Metabolic Pathways

被引:5
作者
Akash, Muhammad Sajid Hamid [1 ]
Sharif, Hina [1 ]
Rehman, Kanwal [2 ]
Rasheed, Sumbal [1 ]
Kamal, Shagufta [3 ]
机构
[1] Govt Coll Univ, Dept Pharmaceut Chem, Faisalabad, Pakistan
[2] Women Univ, Dept Pharm, Multan, Pakistan
[3] Govt Coll Univ, Dept Biochem, Faisalabad, Pakistan
关键词
HbA1c; alpha-amylase; Resveratrol; Hexokinase; Glucose-6-phosphatase; STIMULATED INSULIN-SECRETION; DIABETES-MELLITUS; OXIDATIVE STRESS; GLUCOSE; RESVERATROL; EXPOSURE; MECHANISMS; HYPERGLYCEMIA; TRIVALENT; TOXICITY;
D O I
10.17582/journal.pjz/20220204050235
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
We aimed to investigate the impact of arsenic trioxide (ATO) in impairing carbohydrate metabolism and therapeutic potential of resveratrol (RSV) to treat ATO-induced metabolic disorder. Twenty Wistar rats were used for this study; one group was normal control (NC), second group was exposed to ATO only while the other two groups received metformin (MF) and RSV separately along with ATO. We measured serum levels of glycemic index biomarkers and carbohydrate metabolizing enzymes. Simultaneously, we also measured arsenic concentration in liver using HG-AAS technique. ATO exposed rats showed a significant elevation in serum glucose, reduction in serum insulin, rise in insulin resistance and alteration of carbohydrate metabolizing biomarkers when compared with unexposed rats. Arsenic concentration was found to be significantly high in liver tissues of ATO exposed rats. Contrarily, RSV was found to be effective in regulating normal glycemic level, insulin tolerance, and metabolic biomarkers. Hence, it was found that ATO exposure is correlated with onset of impaired metabolism and RSV can be used as therapeutic intervention for arsenic-induced impaired metabolism.
引用
收藏
页码:2835 / 2844
页数:10
相关论文
共 59 条
[1]   Spice plant Allium cepa: Dietary supplement for treatment of type 2 diabetes mellitus [J].
Akash, Muhammad Sajid Hamid ;
Rehman, Kanwal ;
Chen, Shuqing .
NUTRITION, 2014, 30 (10) :1128-1137
[2]  
Amer Diabet Assoc, 2010, DIABETES CARE, V33, pS11, DOI [10.2337/dc10-S062, 10.2337/dc11-S011, 10.2337/dc10-S011, 10.2337/dc14-S081, 10.2337/dc13-S067, 10.2337/dc12-s064, 10.2337/dc11-S062, 10.2337/dc13-S011, 10.2337/dc12-s011]
[3]   Arsenic and diabetes and hypertension in human populations: A review [J].
Chen, Chien-Jen ;
Wang, Shu-Li ;
Chiou, Jeng-Min ;
Tseng, Chin-Hslao ;
Chiou, Hung-Yi ;
Hsueh, Yu-Mei ;
Chen, Shu-Yuan ;
Wu, Meei-Maan ;
Lai, Mei-Shu .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 222 (03) :298-304
[4]   Arsenic-Induced Pancreatitis [J].
Connelly, Sean ;
Zancosky, Krysia ;
Farah, Katie .
CASE REPORTS IN GASTROINTESTINAL MEDICINE, 2011, 2011
[5]  
de la Lastra CA, 2005, MOL NUTR FOOD RES, V49, P405
[6]   Methylated trivalent arsenicals are potent inhibitors of glucose stimulated insulin secretion by murine pancreatic islets [J].
Douillet, Christelle ;
Currier, Jenna ;
Saunders, Jesse ;
Bodnar, Wanda M. ;
Matousek, Tomas ;
Styblo, Miroslav .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 267 (01) :11-15
[7]  
Duarte-Vazquez M., 2016, J METAB SYND, V5, P1
[8]   Arsenic geochemistry and health [J].
Duker, AA ;
Carranza, EJM ;
Hale, M .
ENVIRONMENT INTERNATIONAL, 2005, 31 (05) :631-641
[9]   Low-Level Arsenic Impairs Glucose-Stimulated Insulin Secretion in Pancreatic Beta Cells: Involvement of Cellular Adaptive Response to Oxidative Stress [J].
Fu, Jingqi ;
Woods, Courtney G. ;
Yehuda-Shnaidman, Einav ;
Zhang, Qiang ;
Wong, Victoria ;
Collins, Sheila ;
Sun, Guifan ;
Andersen, Melvin E. ;
Pi, Jingbo .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2010, 118 (06) :864-870
[10]   Arsenic and diabetes: Current perspectives [J].
Huang, Chun Fa ;
Chen, Ya Wen ;
Yang, Ching Yao ;
Tsai, Keh Sung ;
Yang, Rong Sen ;
Liu, Shing Hwa .
KAOHSIUNG JOURNAL OF MEDICAL SCIENCES, 2011, 27 (09) :402-410