Therapeutic Potential of Dillenia indica L. in Attenuating Hyperglycemia-Induced Oxidative Stress and Apoptosis in Alloxan-Administered Diabetic Mice

被引:7
作者
Sahariah, Plabita [1 ]
Bora, Jutishna [2 ]
Malik, Sumira [2 ,3 ,4 ]
Syiem, Donkupar [1 ]
Bhan, Surya [1 ]
Hussain, Arif [5 ]
Sadier, Najwane Said [6 ]
Rustagi, Sarvesh [3 ]
Haque, Shafiul [7 ,8 ,9 ]
Singh, Nitesh [10 ]
Almutary, Abdulmajeed G. [6 ,11 ]
机构
[1] North Eastern Hill Univ, Dept Biochem, Shillong 793022, Meghalaya, India
[2] Amity Univ Jharkhand, Amity Inst Biotechnol, Ranchi 834002, India
[3] Uttaranchal Univ, Sch Appl & Life Sci, Dehra Dun 248007, Uttarakhand, India
[4] Guru Nanak Coll Pharmaceut Sci, Dehra Dun 248007, Uttarakhand, India
[5] Manipal Acad Higher Educ, Sch Life Sci, Dubai, U Arab Emirates
[6] Abu Dhabi Univ, Coll Hlth Sci, Dept Biomed Sci, Khalifa City 51072, Abu Dhabi, U Arab Emirates
[7] Jazan Univ, Coll Nursing & Allied Hlth Sci, Res & Sci Studies Unit, Jazan 45142, Saudi Arabia
[8] Lebanese Amer Univ, Gilbert & Rose Marie Chagoury Sch Med, Beirut 11022, Lebanon
[9] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, Ajman 13306, U Arab Emirates
[10] Shree Guru Gobind Singh Tricentenary Univ, Fac Agr Sci, Gurugram 122505, Haryana, India
[11] Qassim Univ, Coll Appl Med Sci, Dept Med Biotechnol, Buraydah 51452, Saudi Arabia
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2023年 / 28卷 / 05期
关键词
Dillenia indica extract; HPTLC; alloxan; hyperglycemia; oxidative stress; apoptosis; CASPASE ACTIVATION; CYTOCHROME-C; INSULIN-RESISTANCE; PROTEIN; ACID; BIOCHEMISTRY; MECHANISMS; EXTRACTS; BIOLOGY;
D O I
10.31083/j.fbl2805105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Hyperglycemia-induced oxidative stress accelerates the process of apoptosis in tissues. Dilleniaindica (DI) is a medicinal plant, and its fruit contains many therapeutic properties. The therapeutic activity of the Methanolic Fruit Extract (MFE) of DI in atten-uating oxidative stress and apoptosis in the liver and kidney tissues of alloxan-induced diabetic mice was analyzed in the present study.Methods: High-Performance Thin Layer Chromatography (HPTLC) profiling of MFE was conducted. GLUT4 protein expression anal-ysis and lipid peroxidation assays were conducted to check for MFE effect by administering in diabetic mice. An ultrastructural study was conducted for both the tissues. In apoptotic studies, the TUNEL assay and apoptotic protein expression analysis was conducted.Results: High-Performance Thin Layer Chromatography (HPTLC) profiling of MFE showed the presence of two crucial antioxidants, ascorbic acid, and naringenin. In GLUT-4 protein expression analysis, MFE suppresses hyperglycemia by upregulating GLUT4 protein expression. Lipid peroxidation assay showed a decrease in malondialdehyde (MDA) upon MFE administration in diabetic mice. An ul-trastructural study was conducted, and MFE was found to restore cellular alterations in diabetic tissues. In apoptotic studies, the TUNEL assay shows that MFE treatment showed fewer apoptotic cells than the diabetic group. The study also observed decreased caspase 3 protein expression and increased Bcl-2 protein expression. Conclusions: Therefore, it is inferred from the study that MFE can exert a protective effect by suppressing hyperglycemia and modulating oxidative stress and apoptosis in alloxan-administered diabetic mice.
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页数:13
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