夏草与枸橼酸克罗米芬对镉致大鼠雄性生殖激素毒性影响的比较研究

Justina Nwandimma Nwangwa , Ekementeabasi Aniebo Umoh , Esu Ukpai Enene
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引用次数: 0

摘要

虽然草药与多种功能有关,但草药的化合物及其与这些功能相关的作用机制一直是许多研究人员未能提供的任务。这就是沙蚕的情况及其对雄性动物生殖参数的后续影响。本研究通过对大鼠睾丸激素水平的评估和生物信息学的研究,试图确定沙草活性成分用于改善大鼠生殖系统毒性的第二信使信号通路。取200 ~ 250 g大鼠分为对照组、镉组、高剂量香蒲提取物(HDCE)组、低剂量香蒲提取物(LDCE)组、中剂量香蒲提取物(MDCE)组和克罗米芬实验组( = 5)。所有的动物都可以自由获取食物和水。除对照组外,其他人在四周的给药期间每天饮用3 g/10 L氯化镉溶液。HDCE、MDCE和LDCE分别口服沙草乙醇提取物3750 mg/kg、2500 mg/kg和1250 mg/kg,使用先前公布的LD50结果5000 mg/kg。克罗米芬组给予标准推荐剂量2.8 mg/kg的克罗米芬溶液。采用气相色谱-质谱(GCMS)技术对香草叶提取物中的植物化学成分进行分析,发现峰面积最高的化合物与信号通路酶4UYA (PKC)、4YHJ (PKA)和5IUZ (PKG)对接。给药期结束时,在实验室用异氟醚麻醉处死动物。经心脏穿刺提取血清,采用ELISA试剂盒检测睾酮、卵泡刺激素、黄体生成素和GnRH。的结果中血清睾酮(ng / mL)控制、镉、LDCE, MDCE, HDCE,和Clomid团体意味着± SD 1.13 ±0.02  ng / mL, 0.81±0.08  ng / mL, 0.88±0.09  ng / mL, 0.98±0.10  ng / mL, 1.02±0.07  ng / mL,和1.09 ±0.02  ng / mL,分别。MDCE组、HDCE组和Clomid组的睾酮水平均显著高于镉组,而MDCE组和HDCE组的睾酮水平均显著低于Clomid组(P < <; 0.05),说明Clomid和塞草有改善作用。FSH、LH和GnRH也有相同的改善结果。生物信息学研究表明,石竹烯是香柏草的活性化合物,其峰面积为12.47。此外,克罗米芬与4YHJ具有更强的亲和力和生物活性,石竹烯与5IUZ的结合更强。因此,克罗米芬和柏草通过石竹烯的改善作用可能分别通过cAMP和cGMP第二信使途径。未来的体外研究需要验证这些途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study of the ameliorating effect of Cyperus esculentus and clomiphene citrate on cadmium-induced toxicity on male reproductive hormones in wistar rats
Though herbal remedies have been associated with several functions, the compounds of the herbs and their mechanism of action associated with these functions have always been a task many researchers fail to provide. Such is the case of Cyperus esculentus and its subsequent effect on the reproductive parameters in male animals. This research seeks to ascertain the second messenger signalling pathway through which active compounds of Cyperus esculentus are used to ameliorate toxicity of the reproductive system in rats by assessing hormonal levels of the testis and applying bioinformatics study. Rats of 200–250 g divided into control, cadmium, high-dose cyperus extract (HDCE), low-dose cyperus extract (LDCE), middle-dose cyperus extract (MDCE), and clomid experimental groups (n = 5) were used. All animals were allowed free access to food and water. Except for the control group, others were exposed to a daily 3 g/10 L cadmium chloride solution as their drinking water for the four weeks of administration. HDCE, MDCE, and LDCE received oral Cyperus esculentus ethanolic extract at 3750 mg/kg, 2500 mg/kg, and 1250 mg/kg, respectively, using the previously published LD50 result of 5000 mg/kg. The Clomid group received a solution of Clomid at the standard recommended dose of 2.8 mg/kg. An extract of Cyperus esculentus was assessed for its phytochemical compounds using Gas Chromatography Mass Spectrometry (GCMS) techniques, and compounds with the highest peak area were docked with enzymes of signalling pathways, namely 4UYA (PKC), 4YHJ (PKA), and 5IUZ (PKG). At the end of the administration period, animals were sacrificed in the laboratory using isoflurane anaesthesia. Through cardiac puncture, the serum was extracted for testosterone, FSH, LH, and GnRH assay using ELISA kits. The result of serum testosterone (ng/mL) among the control, cadmium, LDCE, MDCE, HDCE, and Clomid groups in mean ± SD was 1.13 ± 0.02 ng/mL, 0.81 ± 0.08 ng/mL, 0.88 ± 0.09 ng/mL, 0.98 ± 0.10 ng/mL, 1.02 ± 0.07 ng/mL, and 1.09 ± 0.02 ng/mL, respectively. Testosterone levels in the MDCE, HDCE, and Clomid groups were significantly higher than that of Cadmium, whereas those of the MDCE and HDCE were significantly lower than that of the Clomid group at P < 0.05, indicating the ameliorating effect of Clomid and Cyperus esculentus. The same ameliorating results were observed for FSH, LH, and GnRH. A bioinformatics study presented Caryophyllene as the active compound of Cyperus esculentus responsible for its effect following a peak area of 12.47. Furthermore, whereas Clomid showed more affinity and bioactive properties with 4YHJ, caryophyllene binds more with 5IUZ. Therefore, the ameliorating effect of Clomid and Cyperus esculentus through caryophyllene is likely via the cAMP and cGMP second messenger pathways, respectively. Future in vitro studies are required to authenticate these pathways.
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