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Toxicity studies of condensed fuzheng extract in mice and rats.
Wang, JiDa; Wang, Li; Tan, Junzhen; Chai, RunDong; Wang, Ying; Wang, Yue; Zhao, ShuWu; Wang, XiangLing; Bian, YuHong; Liu, JianWei.
Affiliation
  • Wang J; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Wang L; Pharmaceutical Department, Tianjin Second People's Hospital, Tianjin, China.
  • Tan J; Pharmaceutical Department, Tianjin University, Tianjin, China.
  • Chai R; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Wang Y; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Wang Y; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Zhao S; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Wang X; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Bian Y; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
  • Liu J; School of Integrative Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Heliyon ; 10(3): e24780, 2024 Feb 15.
Article in En | MEDLINE | ID: mdl-38318056
ABSTRACT
Nutritional supplements have been used to improve immune function. Condensed fuzheng extract (CFE) is a well-known traditional Chinese medicine (TCM) formula that is predominantly made from sheep placenta, Astragalus mongholicus Bunge, and Polygonatum kingianum Collett & Hemsl. However, the toxicological profile of CFE has not been determined. In this study, we investigated the acute (14 days) and sub-chronic (90 days) oral toxicities of CFE in mice and rats and the phytochemical composition of CFE. Materials and

methods:

For the assessment of acute toxicity, 80 ICR mice of both sexes were randomly divided into four groups. Three groups were treated with 4500, 2250 and 1125 mg/kg/d bw CFE daily (n = 10/group per sex) for 14 days; a separate group was used as control. To test the sub-chronic toxicity, male and female Sprague Dawley rats were orally administered 8150, 4075 or 2037 mg/kg bw of CFE for 90 days; a control group was included. Hematological, biochemical, and histopathological markers were tested at the end of the experiment. The chemical composition of CFE was determined by UPLC-HRMS method.

Results:

In both acute and sub-chronic toxicity studies, no mortalities, indications of abnormality, or treatment-related adverse effects were observed. The LD50 of CFE was higher than 4500 mg/kg. There were no significant changes in the hematological and biochemical data in the treatment group compared with the control group (p > 0.05). Histopathological analyses of the heart, liver, spleen, lungs, kidneys, thymus, testes (male rats) and ovaries (female rats) revealed no anatomical changes of each organ. Phytochemical analysis of CFE revealed the presence of flavonoids (highest abundance), phenols and alkaloids. In conclusion, our results showed that CFE is a safe and non-toxic formula. We also reported phytochemicals in CFE that may possess important pharmacological effects.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Heliyon Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Heliyon Year: 2024 Document type: Article Affiliation country: China
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