菊芋籽油对戊四唑致癫痫发作的保护作用

IF 1 Q4 PHARMACOLOGY & PHARMACY Jundishapur Journal of Natural Pharmaceutical Products Pub Date : 2023-08-21 DOI:10.5812/jjnpp-138748
H. Gavzan, A. Araghi, Ramazan Behzadi
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引用次数: 0

摘要

背景:最近的许多研究表明,多不饱和脂肪酸(PUFA)作为一种安全的补充剂可以提高癫痫发作阈值。然而,补充种子油对癫痫易感性的证据仍然存在争议,其中,Echium种子油(EO)是ω-3和ω-6 PUFA的混合物。目的:本研究旨在测试亚慢性给药EO对静脉注射戊四唑(PTZ)癫痫发作阈值的影响,同时考虑其抗氧化活性和生化参数。方法:将50只雄性小鼠分为5组(每组10只),包括对照组(不治疗)、载体组(芝麻油)和EO组(1、3和5g/kg)。赋形剂和EO每天口服一次,持续四周。然后,确定静脉注射PTZ诱导的癫痫发作阈值。最后,评估血清脂质、肌酸酐、丙氨酸氨基转移酶(ALT)、天冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)的浓度和超氧化物歧化酶(SOD)的活性。结果:与赋形剂相比,EO预处理剂量依赖性地提高了癫痫阈值。EO预处理对血清ALP、AST、ALT、肌酸酐、高密度脂蛋白和低密度脂蛋白浓度无不良影响,但3和5g/kg剂量可降低胆固醇、极低密度脂素(VLDL)(P<0.05)和甘油三酯(TG)(P<0.01),结论:EO预处理可提高癫痫发作阈值,对肝肾生物标志物无负面影响,且对抗氧化活性和血脂水平有积极影响。
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The Protective Effects of the Echium amoenum Seed Oil Against Seizures Induced by Pentylenetetrazole
Background: Many recent studies have documented that polyunsaturated fatty acids (PUFAs) as a safe supplement raise seizure thresholds. However, the evidence of seed oil supplements on seizure susceptibility remains controversial, and among them, Echium seed oil (EO) is a mixture of ω-3 and ω-6 PUFAs. Objectives: This study aimed to test the effects of the sub-chronic administration of EO on intravenous pentylenetetrazole (PTZ) seizure threshold, considering its antioxidant activity and biochemical parameters. Methods: Fifty male mice were divided into five groups (10 in each), including control (no treatment), vehicle (sesame oil), and EO (1, 3, and 5 g/kg) groups. Vehicle and EO were administered p.o. once a day for four weeks. Then, the intravenous PTZ induced-seizure threshold was determined. Finally, the serum concentration of lipid, creatinine, alanine aminotransferase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), and the activity of superoxide dismutase (SOD) was assessed. Results: Pretreatment with EO raised the seizure threshold dose-dependently compared to the vehicle. Pretreatment with EO had no adverse effect on the serum concentration of ALP, AST, ALT, creatinine, high-density lipoprotein (HDL), and low-density lipoprotein (LDL), but at the dosages of 3 and 5 g/kg decreased the concentration of cholesterol, very low-density lipoprotein (VLDL) (P < 0.05), and triglyceride (TG) (P < 0.01). Also, 1 and 3 g/kg of EO improved the activity of SOD (P < 0.01). Conclusions: Pretreatment with EO increases the seizure threshold without negative impacts on the liver and kidney biomarkers, correlated with its positive effects on antioxidant activity and serum lipid profiles.
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