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

J Ethnopharmacol

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

Published: March 2024

AI Article Synopsis

  • Panchvalkala is an Ayurvedic medicine traditionally used for gynecological issues and has shown anticancer potential in cervical cancer cell lines.
  • The study aimed to evaluate the safety of its aqueous extract (PVaq) in Swiss albino mice through a subacute toxicity study over 28 days.
  • Results indicated no significant changes in food consumption, body weight, or vital organ health, suggesting that PVaq does not show acute toxicity in the tested mice.

Article 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.

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Source
http://dx.doi.org/10.1016/j.jep.2023.117332DOI Listing

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