Cucurbita pepo seeds improve peripheral neuropathy in diabetic rats by modulating the inflammation and oxidative stress in rats

被引:2
作者
Kaur, Navpreet [1 ]
Kishore, Lalit [2 ]
Farooq, Shah Asma [1 ]
Kajal, Anu [1 ]
Singh, Randhir [3 ]
Agrawal, Rohini [4 ]
Mannan, Ashi [5 ]
Singh, Thakur Gurjeet [5 ]
机构
[1] MM Univ, MM Coll Pharm, Mullana Ambala 133207, Haryana, India
[2] Univ Ottawa, Fac Hlth Sci, Montreal, ON K1H 8L1, Canada
[3] JSS Acad Tech Educ, Coll Pharm, Noida 201309, Uttar Pradesh, India
[4] Cent Univ Punjab, Dept Pharmacol, Bathinda 151401, India
[5] Chitkara Univ, Chitkara Coll Pharm, Rajpura 140401, Punjab, India
关键词
Cucurbita pepo; Diabetic neuropathy; Streptozotocin; Oxidative stress; Hyperalgesia; NEURONAL DYSFUNCTION; MANAGEMENT; MODEL;
D O I
10.1007/s11356-023-28339-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BackgroundCucurbita pepo (C. pepo) is cultivated and used traditionally as vegetable as well as medicine in different parts of the world. The aim of current study was to investigate the potential of C. pepo in attenuation of diabetic neuropathy via using streptozotocin (STZ)-induced diabetes model in male wistar rats.Materials and MethodsDiabetic neuropathy was induced by administration of STZ; 65 mg/kg, i.p. and Nicotinamide (NAD; 230 mg/kg i.p.) and assessed by measuring thermal hyperalgesia, mechanical hyperalgesia and motor nerve conduction velocity (MNCV) in experimental animals. Treatment with different doses of (100, 200 and 400 mg/kg, p.o.) petroleum ether extract of C. pepo (CPE) and hydroethanolic extract of C. pepo (CHE) was started from the 60(th) day of STZ/NAD administration and continued upto 90(th) day.ResultsCPE and CHE significantly attenuated the behavioural changes including hyperalgesia, allodynia and MNCV linked to diabetic neuropathy. Moreover, the oxidative stress and level of TNF-& alpha;, TGF-& beta; and IL-1 & beta; was found to be significantly attenuated in experimental animals.ConclusionThus C. pepo might ameliorate the progression of diabetic neuropathy via modulation of chronic hyperglycemia and therefore and have therapeutic potential for treatment of diabetic neuropathic pain.
引用
收藏
页码:85910 / 85919
页数:10
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