Facultad de Biología, Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacán, México.
Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacán, México.
Pharm Biol. 2022 Dec;60(1):1384-1393. doi: 10.1080/13880209.2022.2099907.
Skeels (Myrtaceae) exhibits many biological activities.
This study analyzes for the first time, the toxicity, obesogenic, and antioxidant effects of in rats fed with a high fat-fructose diet (HFFD).
Four studies using male Wistar rats were conducted: (a) 7 groups ( = 3): control (corn oil) and ethanol extract of leaf (single oral dose at 100-4000 mg/kg) for acute toxicity; (b) 2 groups ( = 8): control (corn oil) and (1000 mg/kg/day) for 28 days for subacute toxicity; (c) 3 groups ( = 4) with single oral dose of lipid emulsion: control (lipid emulsion), and orlistat (250 and 50 mg/kg, respectively) for lipid absorption; (d) 4 groups ( = 6): control (normal diet) and 3 groups fed with HFFD: HFFD only, and simvastatin (oral dose 250 and 3 mg/kg, respectively) for 13 weeks. Antioxidant enzymes and biomarkers were evaluated and inhibition of pancreatic lipase was determined .
Toxicological studies of showed no differences in biochemical parameters and lethal dose (LD) was higher than 4000 mg/kg. inhibited pancreatic lipase activity, with IC of 392.00 µg/mL, and decreased lipid absorption by 70%. Additionally, it reduced the body weight 22%, restored the activities of antioxidant enzymes, and reduced the biomarkers of oxidative stress.
showed an effect against oxidative stress by reducing biomarkers and induced antioxidant system, without toxic effects.
斯凯尔斯(桃金娘科)表现出许多生物活性。
本研究首次分析了在高脂肪果糖饮食(HFFD)喂养的大鼠中, 的毒性、致肥胖和抗氧化作用。
共进行了四项使用雄性 Wistar 大鼠的研究:(a)7 组(每组 3 只):对照(玉米油)和 叶的乙醇提取物(单次口服 100-4000mg/kg)进行急性毒性试验;(b)2 组(每组 8 只):对照(玉米油)和 (1000mg/kg/天)进行 28 天的亚急性毒性试验;(c)3 组(每组 4 只)单次口服脂质乳剂:对照(脂质乳剂)、 和奥利司他(分别为 250 和 50mg/kg)用于脂质吸收;(d)4 组(每组 6 只):对照(正常饮食)和 3 组 HFFD 喂养:仅 HFFD、 和辛伐他汀(口服剂量分别为 250 和 3mg/kg)喂养 13 周。评估抗氧化酶和生物标志物,并测定胰脂肪酶抑制作用。
的毒理学研究未显示生化参数有差异,且致死剂量(LD)高于 4000mg/kg。 抑制胰脂肪酶活性,IC 为 392.00µg/mL,减少 70%的脂质吸收。此外,它使体重减轻 22%,恢复抗氧化酶的活性,并降低氧化应激的生物标志物。
降低生物标志物并诱导抗氧化系统,显示出抗氧化应激的作用,没有毒性作用。