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首页> 外文期刊>Molecules >Lipolytic Postbiotic from Lactobacillus paracasei Manages Metabolic Syndrome in Albino Wistar Rats
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Lipolytic Postbiotic from Lactobacillus paracasei Manages Metabolic Syndrome in Albino Wistar Rats

机译:来自Lactobacillus paracasei的脂溶性晚期植物在白化Wistar大鼠中管理代谢综合征

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摘要

The current study investigates the capacity of a lipolytic Lactobacillus paracasei postbiotic as a possible regulator for lipid metabolism by targeting metabolic syndrome as a possibly safer anti-obesity and Anti-dyslipidemia agent replacing atorvastatin (ATOR) and other drugs with proven or suspected health hazards. The high DPPH (1,1-diphenyl-2-picrylhydrazyl) and ABTS [2,2′-azino-bis (3-ethyl benzothiazoline-6-sulphonic acid)] scavenging activity and high activities of antioxidant enzyme such as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-px) of the Lactobacillus paracasei postbiotic (cell-free extract), coupled with considerable lipolytic activity, may support its action against metabolic syndrome. Lactobacillus paracasei isolate was obtained from an Egyptian cheese sample, identified and used for preparing the postbiotic. The postbiotic was characterized and administered to high-fat diet (HFD) albino rats (100 and 200 mg kg?1) for nine weeks, as compared to atorvastatin (ATOR; 10 mg kg?1). The postbiotic could correct the disruption in lipid metabolism and antioxidant enzymes in HFD rats more effectively than ATOR. The two levels of the postbiotic (100 and 200 mg kg?1) reduced total serum lipids by 29% and 34% and serum triglyceride by 32–45% of the positive control level, compared to only 25% and 35% in ATOR’s case, respectively. Both ATOR and the postbiotic (200 mg kg?1) equally decreased total serum cholesterol by about 40% and 39%, while equally raising HDL levels by 28% and 30% of the positive control. The postbiotic counteracted HFD-induced body weight increases more effectively than ATOR without affecting liver and kidney functions or liver histopathology, at the optimal dose of each. The postbiotic is a safer substitute for ATOR in treating metabolic syndrome.
机译:目前的研究通过靶向代谢综合征作为可能更安全的抗肥胖和抗血脂血症代价,调查脂溶解的乳杆菌帕拉沙萨氏植物分泌物作为可能的调节剂的脂质代谢作为可能更安全的抗肥胖和抗血脂血症药物替代阿托伐他汀(attor)和其他药物,以证明或可疑的健康危害取代的脂质代谢。高DPPH(1,1-二苯基-2-纤维酰肼)和ABTS [2,2'-唑苯基 - 双(3​​-乙基苯并噻唑啉-6-磺酸)]清除活性和高活性抗氧化酶如超氧化物歧化酶( SOD),乳酸杆菌帕拉卡萨氏菌(无细胞提取物)的过氧化氢酶(猫)和谷胱甘肽过氧化物酶(GSH-PX)与相当大的脂溶性活性相连,可以支持其对代谢综合征的作用。乳酸乳杆菌分离物是从埃及奶酪样品获得的,鉴定并用于制备晚期。与阿托伐他汀(attor; 10mg kgα1)相比,将晚期尿液饮食(HFD)白化大鼠(100和200mg kgα1)施用于九周的高脂饮食(100和200mg kgα1)。晚期后,可以更有效地纠正HFD大鼠脂质代谢和抗氧化酶的破坏。晚期(100和200mg kgβ1)的两种水平将总血清脂质减少29%和34%,血清甘油三酯32-45%的阳性对照水平,而在物品的情况下仅为25%和35% , 分别。 attor和晚期(200mgkg≤1)均匀地降低了总血清胆固醇的约40%和39%,同时将HDL水平同等地升高28%和30%的阳性对照。晚期抵消的HFD诱导的体重比Ator更有效地增加,而不会影响肝肾功能或肝脏组织病理学,在每个的最佳剂量下。晚期是一种更安全的替代物种治疗代谢综合征的替代品。

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