The Protection of Astragalus Polysaccharide in BALB/C Mice during

Astragalus polysaccharide (APS) Brucella infection inflammation

Journal

Immunological investigations
ISSN: 1532-4311
Titre abrégé: Immunol Invest
Pays: England
ID NLM: 8504629

Informations de publication

Date de publication:
29 Aug 2024
Historique:
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: aheadofprint

Résumé

Brucellosis is an important zoonosis worldwide, affecting humans and animals. There are no specific medicines available to treat brucellosis. Astragalus polysaccharide (APS) is derived from Astragalus membranaceus and exhibits impressive bioactivity, including anti-aging, anti-tumor, and immunomodulatory functions. Mice were intraperitoneally inoculated with Brucella melitensis M5 and then treated with APS intraperitoneally injection daily for 7 d. Compared to the M5-infected group, the lower bacteria loads in the APS-treated groups were proved, especially at the acute stage of infection. APS treatment relieved splenomegaly, excess expressions of several pro-inflammatory cytokines (including CXCL1, IFN-γ, IL-1β, IL-2, IL-12p70, and TNF-α). The raised level of IL-4 was observed in APS-treated mice. APS contributed to raising the ratio of M1 macrophage and reducing the ratio of M2 macrophage in the blood. The present study provides some evidence on the potential application of APS in controlling and treating brucellosis and should be further explored.

Identifiants

pubmed: 39206848
doi: 10.1080/08820139.2024.2380718
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

Yuanqiang Zheng (Y)

School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Inner Mongolia Key Laboratory of Molecular Biology, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.

Yajing Chen (Y)

Inner Mongolia Key Laboratory of Molecular Biology, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.

Jianlong Zhao (J)

ABSL-3 laboratory, Jinyu Baoling Bio-Pharmaceutical Co. Ltd., Hohhot, Inner Mongolia, China.

Meihua Wu (M)

ABSL-3 laboratory, Jinyu Baoling Bio-Pharmaceutical Co. Ltd., Hohhot, Inner Mongolia, China.

Ligao Bao (L)

ABSL-3 laboratory, Jinyu Baoling Bio-Pharmaceutical Co. Ltd., Hohhot, Inner Mongolia, China.

Dantong Zhao (D)

ABSL-3 laboratory, Jinyu Baoling Bio-Pharmaceutical Co. Ltd., Hohhot, Inner Mongolia, China.

Shuang Bai (S)

Department of Dermatology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.

Dongdong Di (D)

ABSL-3 laboratory, Jinyu Baoling Bio-Pharmaceutical Co. Ltd., Hohhot, Inner Mongolia, China.

Yanchun Shi (Y)

Inner Mongolia Key Laboratory of Molecular Biology, Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.

Classifications MeSH