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标准化阿育吠陀配方-Panchvalkala 的亚急性毒性研究的安全性评价。

Safety evaluation of standardized Ayurvedic formulation-Panchvalkala, by subacute toxicity study.

机构信息

Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth (Deemed to be University), Katraj-Dhankawadi, Pune-Satara Road, Katraj, Pune, 411043, Maharashtra, India; Department of Pharmaceutical Biotechnology, Poona College of Pharmacy, Bharati Vidyapeeth Deemed to be University, Erandwane, Pune, 411038, India.

Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth (Deemed to be University), Katraj-Dhankawadi, Pune-Satara Road, Katraj, Pune, 411043, Maharashtra, India; Symbiosis School of Biological Sciences (SSBS), Symbiosis International (Deemed University), Gram, Lavale, 412115, India.

出版信息

J Ethnopharmacol. 2024 Mar 1;321:117332. doi: 10.1016/j.jep.2023.117332. Epub 2023 Oct 17.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Panchvalkala is a conventional Ayurvedic medicine used as a douche in gynecological disorders such as leucorrhea, infertility, and endometriosis. Recently, we have reported the anticancer activity of Panchvalkala aqueous extract (PVaq) in cervical cancer cell lines, SiHa (HPV16+), HeLa (HPV18+), and mouse papilloma models.

AIM OF THE STUDY

Here, we have evaluated the safety of the aqueous extract of Ayurvedic formulation, Panchvalkala (PVaq), in Swiss albino mice by performing subacute toxicity study.

MATERIALS AND METHODS

Male and female Swiss albino mice (n = 5/sex/group) were gavaged orally with different doses of PVaq for 28 consecutive days. The mice were distributed into six groups: I (vehicle control), II (vehicle control reversal), III (PVaq 250 mg/kg), IV (PVaq 500 mg/kg), V (1000 mg/kg) and VI (1000 mg/kg high dose reversal). Animals were observed periodically to record any clinical signs of toxicity or mortality. After completion of treatment and recovery periods, animals were evaluated for the effect of PVaq on urine parameters, followed by hematological and biochemical parameters. Animals were sacrificed on day 29 for gross observation of vital organs and to study their histopathology. Reversal groups were maintained for further 14 days to observe any delayed onset of toxic side effects or reversal of toxicity, followed by sacrificing the mice on day 43.

RESULTS

In the subacute toxicity study, PVaq did not show any significant change in food, water consumption, and body weights. There were no significant alterations in hematology, biochemistry, urine parameters, and histopathology of the analyzed tissues (brain, heart, liver, lung, spleen, thymus, kidney, epididymis/ovaries, and testis/uterus). The parameters were comparable to their respective controls in both the female as well as the male mice groups. Upon macroscopic and microscopic observation of vital organs, no abnormality was detected compared to the respective control groups.

CONCLUSION

The subacute toxicity study demonstrated that oral administration of PVaq was safe in female and male Swiss albino mice.

摘要

民族药理学相关性

Panchvalkala 是一种传统的阿育吠陀药物,用于治疗妇科疾病,如白带、不孕和子宫内膜异位症。最近,我们报道了 Panchvalkala 水提取物(PVaq)在宫颈癌细胞系、SiHa(HPV16+)、HeLa(HPV18+)和小鼠乳头瘤模型中的抗癌活性。

研究目的

在这里,我们通过进行亚急性毒性研究,评估了阿育吠陀配方 Panchvalkala(PVaq)的水提取物在瑞士白化病小鼠中的安全性。

材料和方法

雄性和雌性瑞士白化病小鼠(n=5/性别/组)连续 28 天口服不同剂量的 PVaq。将小鼠分为六组:I(载体对照)、II(载体对照逆转)、III(PVaq 250mg/kg)、IV(PVaq 500mg/kg)、V(1000mg/kg)和 VI(1000mg/kg 高剂量逆转)。定期观察动物以记录任何毒性或死亡的临床症状。治疗和恢复期结束后,评估 PVaq 对尿液参数的影响,然后进行血液学和生化学参数评估。第 29 天处死动物,对重要器官进行大体观察,并研究其组织病理学。逆转组维持 14 天,以观察任何迟发性毒性副作用或毒性逆转,然后在第 43 天处死小鼠。

结果

在亚急性毒性研究中,PVaq 对食物、水的消耗和体重没有显著影响。血液学、生化学、尿液参数和分析组织(脑、心、肝、肺、脾、胸腺、肾、附睾/卵巢和睾丸/子宫)的组织病理学没有显著改变。在雌性和雄性小鼠组中,这些参数与各自的对照组相当。与各自的对照组相比,在重要器官的大体和显微镜观察中没有发现异常。

结论

亚急性毒性研究表明,口服 PVaq 在雌性和雄性瑞士白化病小鼠中是安全的。

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