Preclinical renal chemo-protective potential of Prunus amygdalus Batsch seed coat via alteration of multiple molecular pathways

被引:12
作者
Pandey, Preeti [1 ]
Bhatt, Prakash Chandra [2 ]
Rahman, Mahfoozur [1 ]
Patel, Dinesh Kumar [1 ]
Anwar, Firoz [3 ]
Al-Abbasi, Fahad [3 ]
Verma, Amita [4 ]
Kumar, Vikas [1 ]
机构
[1] Sam Higginbottom Univ Agr Technol & Sci, Dept Pharmaceut Sci, Nat Prod Drug Discovery Lab, Fac Hlth Sci, Allahabad, Uttar Pradesh, India
[2] Jamia Hamdard, Microbial & Pharmaceut Biotechnol Lab, Fac Pharm, Ctr Adv Res Pharmaceut Sci, New Delhi, India
[3] King Abdulaziz Univ, Dept Biochem, Fac Sci, Jeddah, Saudi Arabia
[4] Sam Higginbottom Univ Agr Technol & Sci, Dept Pharmaceut Sci, Bioorgan & Med Chem Res Lab, Fac Hlth Sci, Allahabad, Uttar Pradesh, India
关键词
Green almond; renal cancer; inflammatory mediator; macroscopical observation; NITRILOTRIACETATE FE-NTA; OXIDATIVE STRESS; TUMOR PROMOTION; HYPERPROLIFERATIVE RESPONSE; CHEMOPREVENTIVE EFFICACY; INDUCED NEPHROTOXICITY; ANTIOXIDANT ACTIVITY; INDUCED ARTHRITIS; EARLY MARKERS; CARCINOGENESIS;
D O I
10.1080/13813455.2017.1364773
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
Prunus amygdalus Batsch (almond) is a classical nutritive traditional Indian medicine. Along with nutritive with anti-oxidant properties, it is, clinically, used in the treatment of various diseases with underlying anti-oxidant mechanism. This study is an effort to scrutinise the renal protective effect of P. amygdalus Batsch or green almond (GA) seed coat extract and its underlying mechanism in animal model of Ferric nitrilotriacetate (Fe-NTA) induced renal cell carcinoma (RCC). RCC was induced in Swiss Albino Wistar rats by intraperitoneal injection of Fe-NTA. The rats were then treated with ethanolic extract of GA (25, 50 and 100 mg/kg per oral) for 22 weeks. Efficacy of GA administration was evaluated by change in biochemical, renal, macroscopical and histopathological parameters and alterations. Additionally, interleukin-6 (IL-6), tumour necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta) and inflammatory mediator including prostaglandin E2 (PGE(2)), nuclear factor-kappa B (NF-kappa B) were also observed to explore the possible mechanisms. The oral administration of GA significantly (p<.001) altered the Fe-NTA induced RCC in rats by inhibition of renal nodules, decolourisation of tissues, tumour promoter marker including thymidine (3)[H] incorporation, ornithine decarboxylase, renal parameters and anti-oxidant parameters in serum. Additionally, GA treatment significantly (p<.001) down-regulated the IL-6, IL-1 beta, TNF-alpha, inflammatory mediators PGE(2) and NF-kappa B in a dose-dependent manner. Histopathology observation supported the renal protective effect of GA by alteration in necrosis, size of Bowman capsules and inflammatory cells. Hence, it can be concluded that GA possesses observable chemo-protective action and effect on Fe-NTA induced RCC via dual inhibition mechanism one by inhibiting free radical generation and second by inhibiting inflammation.
引用
收藏
页码:88 / 96
页数:9
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