Startseite Acute and sub-acute toxicity assessment of the standardized extract of Sanguisorba minor in vivo
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Acute and sub-acute toxicity assessment of the standardized extract of Sanguisorba minor in vivo

  • Legha Ansari , Mohammad Reza Mahdinezhad , Hassan Rakhshandeh , Azar Hosseini , Samaneh Boroumand Noughabi , Najibeh Gholami und Arezoo Rajabian EMAIL logo
Veröffentlicht/Copyright: 6. Dezember 2021

Abstract

Although Sanguisorba minor has been used as herbal medicine, no study has ever examined its potential toxicity. This study investigated acute and subacute toxicities of S. minor hydroalcoholic extract (SE). In the acute toxicity test, a single oral dose (300, 2,000, and 3,000 mg/kg) of SE was given to mice. The oral administration of SE (100, 200, and 400 mg/kg for 4 weeks) was performed to evaluate subacute toxicity. After the treatments, neurobehavioral, histopathology, hematological, and biochemical parameters were monitored. In vitro cytotoxicity was also assessed. Moreover, high-performance liquid chromatography fingerprint was done for the standardization of SE. The no-observed-adverse-effect level of SE was up to 2,000 mg/kg, and the LD50 of the prepared extract was over 3,000 mg/kg. The rats exposed to the extract did not show any marked change in their body weight. The extract at used doses did not affect neuromuscular coordination. According to the hematological, biochemical, and histological examinations, no significant treatment-related adverse effect of the extract was observed, even at 400 mg/kg. Only 48 h exposure to 400 μg/mL of SE reduced the viability of PC12 cells. The findings revealed that this plant could be well-tolerated, regarded safe, and used as herbal medicine.


Corresponding author: Arezoo Rajabian, Department of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran; and Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran, Phone: +98 38828265, Fax: +98 51 38828567, E-mail:

Funding source: Mashhad University of Medical Sciences

Award Identifier / Grant number: 990641

Acknowledgments

This study was originated from a MD project of Najibeh Gholami.

  1. Research funding: This project was financially supported by Vice Chancellery for Research and Technology, Mashhad University of Medical Sciences with Grant No. 990641.

  2. Author contributions: Arezoo Rajabian: Conceptualization, Methodology, providing revision of the manuscript. Legha Ansari, Mohammad Reza Mahdinezhad, Najibeh Gholami: Acquisition of data, Data curation, Writing-Original draft preparation. Arezoo Rajabian, Samaneh Boroumand Noughabi: Analysis and/or interpretation of data, Investigation. Arezoo Rajabian, Hassan Rakhshandeh: Supervision: Arezoo Rajabian, Azar Hosseini: Reviewing and Editing.

  3. Competing interests: The authors declare that they have no conflict of interest.

  4. Informed consent: Not applicable.

  5. Ethics approval: All procedures are in agreement with Guidelines for Care and Use of Laboratory Animals, National Institutes of Health, and confirmed by the Institutional Animal Care and Use Committee of MUMS (Ethical code: IR.MUMS.REC.1399.388).

  6. Data availability: The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Received: 2021-08-27
Accepted: 2021-11-15
Published Online: 2021-12-06

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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