Safety assessment of hydro-ethanolic extract of Falcaria vulgaris in Wistar rats: Acute and subchronic toxicities

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Journal of Reports in Pharmaceutical Sciences Pub Date : 2022-07-01 DOI:10.4103/jrptps.jrptps_15_22
Meinoush Haghighi, M. Arya, M. Mojarrab, Z. Rahimi, Marzieh Hajialyni, L. Hosseinzadeh, N. Amin, Fereshteh Jalilian
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Abstract

Background: Falcaria vulgaris is a medicinal plant with culinary uses and widespread therapeutic applications. Despite already proven as a very promising dietary supplement, its safety and possible effects on the human body are yet to define. This study was designed to investigate the acute and subchronic toxic effects of hydroethanolic F. vulgaris in male and female Wistar rats. Experimental: To evaluate the safety of a hydroethanolic extract of F. vulgaris, acute and subchronic toxicity in Wistar rats treated with extract was investigated. For investigation of acute toxicity of F. vulgaris, both genders of rats were treated for 45 days with a single dose of the extract (4000 mg/kg) via gavage. Also for sub-chronic testing, the extract was administrated orally at the doses of 150, 300, and 450 mg/kg for 45 days. At the end of the study, the animals were sacrificed and the hematological, biochemical, and histopathological parameters were assayed. Results: After a single oral administration of F. vulgaris (4000 mg/kg), no mortality was observed in both control and groups in either sex. Also, histopathological inspection of vital organs and tissues revealed no obvious alteration in these organs. The obtained results showed a significant reduction in the weight of heart and liver in male rats that received the highest dose of the extract. The level of red blood cell distribution width (dose of 450 mg/kg) from the hematological parameters and the level of serum creatinine (dose of 150 and 450 mg/kg) from the biochemical parameters increased significantly in male rats. On the contrary, during treatment the concentration of all examined minerals remained unchanged. Histopathological inspection indicated that liver, kidney, and testis were found to be affected by subchronic exposure to F. vulgaris extract. Conclusion: The results of the acute study revealed that F. vulgaris may be nontoxic even at doses less than 4000 mg/kg body weight. However, the result of subchronic study confirmed the liver dysfunctions in Wistar rats and also suggested the significant effect of F. vulgaris on testicular tissue, which may cause serious male infertility. The ability to impair male fertility by such a medicinal plant has not been reported yet. It can be concluded that the no observed adverse effect level (NOAEL) of F. vulgaris are 150 and 450 mg/kg for male and female rats, respectively.
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寻常Falcaria vulgaris水乙醇提取物对Wistar大鼠的安全性评价:急性和亚慢性毒性
背景:蚕豆是一种具有烹饪用途和广泛治疗应用的药用植物。尽管已经被证明是一种非常有前景的膳食补充剂,但其安全性和对人体的可能影响尚待确定。本研究旨在研究水乙醇对雄性和雌性Wistar大鼠的急性和亚慢性毒性作用。实验:为了评价寻常F.vulgaris水乙醇提取物的安全性,研究了该提取物对Wistar大鼠的急性和亚慢性毒性。为了研究寻常F.vulgaris的急性毒性,用单剂量提取物(4000 mg/kg)。同样对于亚慢性测试,提取物以150、300和450 mg/kg的剂量口服给药45天。研究结束时,处死动物,测定血液学、生化和组织病理学参数。结果:单次口服寻常F.vulgaris(4000 mg/kg),在对照组和组中均未观察到任何性别的死亡率。此外,对重要器官和组织的组织病理学检查显示,这些器官没有明显变化。所获得的结果显示,接受最高剂量提取物的雄性大鼠的心脏和肝脏重量显著减轻。红细胞水平分布宽度(剂量450 mg/kg)和血清肌酸酐水平(150和450的剂量 mg/kg)显著增加。相反,在处理过程中,所有检查矿物的浓度保持不变。组织病理学检查表明,肝脏、肾脏和睾丸受到亚慢性暴露于寻常草提取物的影响。结论:急性研究的结果表明,即使剂量低于4000,寻常F.vulgaris也可能是无毒的 mg/kg体重。然而,亚慢性研究的结果证实了Wistar大鼠的肝功能紊乱,也表明了寻常F.vulgaris对睾丸组织的显著影响,这可能导致严重的雄性不育。这种药用植物损害雄性生殖能力的能力还没有报道。可以得出结论,对于雄性和雌性大鼠来说,寻常F.vulgaris的未观察到的不良反应水平(NOAEL)分别为150和450 mg/kg。
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来源期刊
Journal of Reports in Pharmaceutical Sciences
Journal of Reports in Pharmaceutical Sciences Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.40
自引率
0.00%
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0
期刊介绍: The Journal of Reports in Pharmaceutical Sciences(JRPS) is a biannually peer-reviewed multi-disciplinary pharmaceutical publication to serve as a means for scientific information exchange in the international pharmaceutical forum. It accepts novel findings that contribute to advancement of scientific knowledge in pharmaceutical fields that not published or under consideration for publication anywhere else for publication in JRPS as original research article. all aspects of pharmaceutical sciences consist of medicinal chemistry, molecular modeling, drug design, pharmaceutics, biopharmacy, pharmaceutical nanotechnology, pharmacognosy, natural products, pharmaceutical biotechnology, pharmacology, toxicology and clinical pharmacy.
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