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睡莲(睡莲科)花水提取物的安全性评估:对白化Wistar大鼠的急性、神经和亚慢性经口毒性研究

Safety assessment of the aqueous extract of the flowers of Nymphaea lotus Linn (Nymphaeaceae): Acute, neuro- and subchronic oral toxicity studies in albinos Wistar rats.

作者信息

Kameni Poumeni Mireille, Bilanda Danielle Claude, Dzeufiet Djomeni Paul Désiré, Mengue Ngadena Yolande Sandrine, Mballa Marguerite Francine, Ngoungoure Madeleine Chantal, Ouafo Agnès Carolle, Dimo Théophile, Kamtchouing Pierre

出版信息

J Complement Integr Med. 2017 Mar 24;14(2). doi: 10.1515/jcim-2016-0046.

DOI:10.1515/jcim-2016-0046
PMID:28291734
Abstract

Background Nymphaea lotus Linn (N. lotus) is a medicinal plant widely used in Cameroon popular medicine, to treat neuropsychiatric conditions, male sexual disorders or as food supplement. However, scientific data on the pharmacotoxic profile of this plant are not available. The safety of N. lotus was assessed in acute, neuro- and subchronic toxicity studies by following the OECD guidelines. Effectively, no data have been published until now in regard to its safety on the nervous system. Methods Aqueous extract of N. lotus at doses of 200, 400 and 600 mg/kg body weight (BW) was evaluated for nitrites contents and orally administered to rats daily for 28 days (5 male, 5 female per group). The control group received distilled water (10 mL/kg) and a satellite group was used to observe reversal effects. Neurotoxicity of the plant was determined using open field test for motor coordination, ataxia and gait analysis. Clinical signs and state of livelihood were recorded during the 24 h, then for 28 days of treatments. At the end of 28-day period, animals were anesthetized and decapitated. The whole brain was homogenized for neurobiochemical analysis. Blood samples were collected with or without anticoagulant for hematological examinations and serum analysis. Specimens of liver, kidney, testis, ovaries, and brain were fixed in 10 % formalin and processed for histopathological examinations. Results Our findings indicate dose-dependent elevation of nitrites contents in the flowers aqueous extract of N. lotus. Acute toxicity study revealed no signs of toxicity neither at the dose 2,000 mg/kg nor at 5,000 mg/kg. Thus the LD50 value of aqueous extract of N. lotus flowers is superior to 5,000 mg/kg. The repeated administration of N. lotus during 28 days, induced no signs of neurobehavioral changes in male, but female rats exhibited dose-dependent response in the open field test, suggesting sex and dose-relative psychotropic effects of N. lotus. The evaluation of neurobiochemistry revealed consistent rise of brain cholesterol by 44.05 %; 158.10 % and 147.62 % respectively in male rats treated with the doses of 200, 400 and 600 mg/kg. In female rats, these levels were significantly increased (p<0.001) only at the dose of 600 mg/kg compared to control. This trend persisted after 14 days withdrawal. Brain potassium and calcium concentrations were increased in all rats compared to their respective control receiving distilled water, suggesting transmembrane current stabilizing properties of brain cells by our extract. Further, serum biochemical analysis demonstrated that 28-day administration of N. lotus flowers increased depending on the dose and sex, the levels of serum urea, proteins, creatinine and bilirubin and reduced γ-glutamyltransferase (GGT) and alkaline phosphatase (ALP) activities. These results suggest liver alterations that are endowed by lower liver relative weight and histology damages observed in female rats treated with the dose of 600 mg/kg of our extract. We also observed a rise in the low-density lipoprotein (LDL) fraction and AI of male rats undergoing N. lotus treatment. In female rats, the latter remains unaltered, confirming the dose- and sex-dependent response of our extract. The levels of white blood cells (WBC) and granulocytes were higher in male irrespective to their control, revealing stimulatory properties of the male hematopoietic system. Such variations (sex- and dose-dependent) are without biological relevance for the majority of the biochemical parameters evaluated, indicating a wide margin of safety for the traditional use of N. lotus. The alkaloids, nitrites and phytosterols contained in N. lotus flowers extract may probably account for its neuroprotective, anti-oxidant, and immunoboosting properties. Conclusions N. lotus do not possesses neurotoxicity but is able to induce behavioral changes in rats. Therefore, the application of this plant as either drug or supplementary food should be carefully considered.

摘要

背景

莲(睡莲科莲属植物)是一种药用植物,在喀麦隆传统医学中广泛用于治疗神经精神疾病、男性性功能障碍或作为食品补充剂。然而,关于这种植物的药物毒性概况的科学数据尚不可得。按照经济合作与发展组织(OECD)的指导方针,在急性、神经和亚慢性毒性研究中评估了莲的安全性。实际上,迄今为止尚未发表关于其对神经系统安全性的数据。

方法

评估莲水提取物中剂量为200、400和600毫克/千克体重(BW)时的亚硝酸盐含量,并每天口服给予大鼠,持续28天(每组5只雄性、5只雌性)。对照组接受蒸馏水(10毫升/千克),并使用一个卫星组观察逆转效应。通过旷场试验来测定植物的神经毒性,以评估运动协调性、共济失调和步态分析。在24小时内记录临床症状和生存状态,然后在治疗的28天内进行记录。在28天治疗期结束时,对动物进行麻醉并断头。将整个大脑匀浆用于神经生化分析。采集有或没有抗凝剂的血液样本用于血液学检查和血清分析。将肝脏、肾脏、睾丸、卵巢和大脑标本固定在10%福尔马林中,并进行组织病理学检查。

结果

我们的研究结果表明,莲花朵水提取物中的亚硝酸盐含量呈剂量依赖性升高。急性毒性研究显示,在2000毫克/千克和5000毫克/千克剂量下均未出现毒性迹象。因此,莲花水提取物的半数致死量(LD50)值高于5000毫克/千克。连续28天给予莲,雄性大鼠未出现神经行为变化的迹象,但雌性大鼠在旷场试验中表现出剂量依赖性反应,表明莲具有性别和剂量相关的精神otropic作用。神经生化评估显示,分别用200、400和600毫克/千克剂量处理的雄性大鼠大脑胆固醇含量分别持续升高44.05%、158.10%和147.62%。在雌性大鼠中,与对照组相比,仅在600毫克/千克剂量下这些水平显著升高(p<0.001)。停药14天后这种趋势仍然存在。与接受蒸馏水的各自对照组相比,所有大鼠的脑钾和钙浓度均升高,表明我们的提取物具有稳定脑细胞跨膜电流的特性。此外,血清生化分析表明,连续28天给予莲花提取物会根据剂量和性别增加血清尿素、蛋白质、肌酐和胆红素水平,并降低γ-谷氨酰转移酶(GGT)和碱性磷酸酶(ALP)活性。这些结果表明存在肝脏改变,这表现为肝脏相对重量降低以及在接受600毫克/千克提取物处理的雌性大鼠中观察到的组织学损伤。我们还观察到接受莲治疗的雄性大鼠低密度脂蛋白(LDL)分数和动脉粥样硬化指数(AI)升高。在雌性大鼠中,后者保持不变,证实了我们提取物的剂量和性别依赖性反应。无论对照组如何,雄性大鼠的白细胞(WBC)和粒细胞水平都较高,表明雄性造血系统具有刺激特性。对于大多数评估的生化参数而言,这种(性别和剂量依赖性)变化没有生物学相关性,表明莲在传统使用中具有广泛的安全范围。莲花提取物中含有的生物碱、亚硝酸盐和植物甾醇可能是其具有神经保护、抗氧化和免疫增强特性的原因。

结论

莲不具有神经毒性,但能够在大鼠中引起行为变化。因此,应谨慎考虑将这种植物用作药物或补充食品。

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