Therapeutic potential of bark extracts from Macaranga denticulata on renal fibrosis in streptozotocin-induced diabetic rats

被引:1
作者
Gali, Sreevarsha [1 ]
Kundu, Amit [1 ,2 ]
Sharma, Swati [1 ]
Ahn, Mee-Young [3 ]
Puia, Zothan [4 ]
Kumar, Vikas [5 ]
Kim, In Su [1 ]
Kwak, Jeong Hwan [1 ]
Palit, Partha [6 ]
Kim, Hyung Sik [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm Univ, Sch Pharm, Suwon, South Korea
[2] GITAM, GITAM Sch Pharm, Dept Pharmacol, Visakhapatnam, Andhra Pradesh, India
[3] Changwon Natl Univ, Dept Biochem & Hlth Sci, Changwon Si, South Korea
[4] Reg Inst Paramed & Nursing Sci, Dept Pharm, Aizawl, India
[5] Sam Higginbottom Inst Agr Technol & Sci, Dept Pharmaceut Sci, Nat Prod Drug Discovery Lab, Fac Hlth Sci, Allahabad, Uttar Pradesh, India
[6] Assam Univ, Dept Pharmaceut Sci, Drug Discovery Res Lab, Silchar, India
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2024年 / 87卷 / 23期
基金
新加坡国家研究基金会;
关键词
Diabetic nephropathy; Macaranga denticulata; renal fibrosis; oxidative stress; inflammation; streptozotocin; PRENYLATED FLAVONOIDS; INSULIN-RESISTANCE; OXIDATIVE STRESS; KIDNEY-DISEASE; MESANGIAL CELL; NEPHROPATHY; INJURY; SIRT1; INFLAMMATION; PROTECTS;
D O I
10.1080/15287394.2024.2394586
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Macaranga denticulata (MD) bark is commonly utilized in traditional medicine for diabetes prevention and treatment. The bark extract of MD is rich in prenyl or farnesyl flavonoids and stilbenes, which possess antioxidant properties. Although data suggest the potential therapeutic benefits of the use of MD in treating diabetic nephropathy (DN), the precise mechanisms underlying MD-initiated protective effects against DN are not well understood. This study aimed to assess the renoprotective properties of MD extract by examining renofibrosis inhibition, oxidative stress, and inflammation utilizing streptozotocin-induced DN male Sprague - Dawley rats. Diabetic rats were intraperitoneally injected with streptozotocin (STZ) to induce diabetes. After 6days, these rats were orally administered MD extract (200mg/kg/day) or metformin (200mg/kg/day) for 14days. The administration of MD extract significantly lowered blood glucose levels, restored body weight, and reduced urine levels of various biomarkers associated with kidney functions. Histopathological analysis revealed protective effects in both kidneys and pancreas. Further, MD extract significantly restored abnormalities in advanced glycation end products, oxidative stress biomarkers, and proinflammatory cytokine levels in STZ-treated rats. MD extract markedly reduced renal fibrosis biomarker levels, indicating recovery from renal injury, and reversed dysregulation of sirtuins and claudin-1 in the kidneys of rats with STZ-induced diabetes. In conclusion, data demonstrated the renoprotective role of MD extract, indicating plant extract's ability to suppress oxidative stress and regulate proinflammatory pathways during pathological changes in diabetic nephropathy. [GRAPHICS] .
引用
收藏
页码:911 / 933
页数:23
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