Dietary flaxseed oil and fish oil ameliorates renal oxidative stress, protein glycation, and inflammation in streptozotocin-nicotinamide-induced diabetic rats

被引:34
|
作者
Jangale, Nivedita M. [1 ]
Devarshi, Prasad P. [2 ]
Bansode, Sneha B. [3 ]
Kulkarni, Mahesh J. [3 ]
Harsulkar, Abhay M. [1 ]
机构
[1] Bharati Vidyapeeth Deemed Univ, Poona Coll Pharm, Dept Pharmaceut Biotechnol, Pune 411038, Maharashtra, India
[2] Bharati Vidyapeeth Deemed Univ, Interact Res Sch Hlth Affairs, Pune 411043, Maharashtra, India
[3] CSIR, Natl Chem Lab, Div Biochem Sci, Prote Facil, Pune 411008, Maharashtra, India
关键词
Diabetes; Flaxseed oil; Fish oil; Kidney; Glycation; Streptozotocin; POLYUNSATURATED FATTY-ACIDS; EICOSAPENTAENOIC ACID; KKA(Y)/TA MICE; NEPHROPATHY; RAGE; INVOLVEMENT; ACTIVATION; RECEPTOR; MODEL;
D O I
10.1007/s13105-016-0482-8
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
Protective and prophylactic effects of omega-3 fatty acids on oxidative stress and inflammation are well known. We assessed beneficial effects of flaxseed oil and fish oil on streptozotocin (65 mg/kg; i.p.)-nicotinamide (110 mg/kg; i.p.) induced diabetic rats by studying renal expression of antioxidant and inflammatory genes. Diabetic rats given 10 % flaxseed oil or 10 % fish oil diet for 35 days showed significant decrease in renal lipid peroxidation. Flaxseed oil diet resulted in up-regulation of renal superoxide dismutase-1 (SOD-1) (activity and expression) and glutathione peroxidase-1 (GPx-1) expression. Furthermore, both diets up-regulated catalase (CAT) (activity and expression) and down-regulated heme oxygenase-1 (HO-1) expression. Both diets were able to limit the renal advanced glycation end products (AGEs) formation and reduced receptor of AGE (RAGE) protein expression significantly. Expressions of interleukin-6 (IL-6) and NF-kappa B p65 subunit were down-regulated significantly by flaxseed oil or fish oil diet. The histological tubular injuries were also lowered by both diets. These results suggest that dietary omega-3 fatty acids may slow the progression of diabetic nephropathy (DN) associated with oxidative stress, glycation, and inflammation in the kidney.
引用
收藏
页码:327 / 336
页数:10
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