Tupistra chinensis
Polysaccharide Strengthened Immunity in Mice Induced by
Cyclophosphamide Via Regulating Microbiota
Qing He1, Xinru Wang1,2, Tao Luo1,3,4, Hadil
Alkathiry5,Manal
Abduallah Alduwish6, Mahmoud
M. Abdelwahab7,
Wentong Liu2*,
Huijuan Sun3*
and
Quzhen Deji4*
1College
of Veterinary Medicine, Nanjing Agricultural University, Nanjing
210095, China; 2School of Basic Medicine, Hubei
University of Arts and Science, Xiangyang
441000,
China;3Innovation Center for Edible Fungi Resources and
Application Technology, Xizang Autonomous Region, Lhasa 850000,
China;
4Institute
of Animal Husbandry and Veterinary Medicine, Xizang Academy of
Agricultural and Animal Husbandry Sciences, Lhasa 850009, China;
5Department
of Biology, College of Science, Imam Mohammad Ibn Saud Islamic
University (IMSIU), Riyadh, Saudi Arabia;
6Department
of Biology, College of Science and Humanities in Al-Kharj, Prince
Sattam Bin Abdulaziz University, Alkarj 11942, Saudi Arabia; 7Department
of Mathematics and Statistics, Faculty of Science, Imam Mohammad Ibn
Saud Islamic University (IMSIU), Riyadh 11432, Saudi Arabia.
The effect of Tupistra chinensis
polysaccharide on the immunity and microbiota of mice induced by
cyclophosphamide
(CTX)
in mice
was investigated.
In total, forty ICR mice aged about 4 weeks were randomly divided into 4 groups
(n=10/group)
with blank control group (CCAR), immune deficiency model group (MCAR), positive
control group (LHAR), and Tupistra chinensis polysaccharide group (PCAR).
Mice in the MCAR, LHAR, and PCAR groups received intraperitoneal injections of
CTX for 3 consecutive days. Additionally, from the fourth day, 0.2mL of normal
saline was given to mice in the CCAR and MCAR groups, while 40mg/kg of
levamisole (LH) was administered to mice in the LHAR group daily; likewise, mice
in the PCAR group were given 100mg/kg Tupistra chinensis polysaccharide
(TCP) every day, for 14 days. Serum biochemistry, H&E staining, and gut
microbiome sequencing indicated that TCP significantly alleviated CTX-induced
immune dysfunction. Malondialdehyde levels in the TCP-treated group were lower
than those in the model group. In contrast, interleukin(IL)-6,
tumor necrosis factor-alpha,
IL-1beta, IL-10,
total antioxidant capacity, and superoxide dismutase levels were higher in the
TCP-treated group compared to the model group. The sequencing data showed that
TCP supplementation restored the intestinal microbiome and its function in mice
with CTX-induced changes. TCP down-regulated the abundance of noxious microbes,
such as Dwaynesavagella,Streptococcus, and Duncaniella,
and there was an increase in the beneficial bacteria like Limosilactobacillus
and Ligilactobacillus in the gut. It was concluded that TCP has a
restorative effect on CTX-induced immune dysfunction in mice by regulating
oxidative stress and restoring the intestinal microbiome.
To Cite This Article:
He Q, Wang X, Luo T, Alkathiry H,Alduwish MH, Abdelwahab MM, Liu W,
Sun H
and
Deji Q,
2026. Tupistra chinensis
polysaccharide strengthened immunity in mice induced by cyclophosphamide via
regulating microbiota.
Pak Vet J, 46(5): 1313-1323.
http://dx.doi.org/10.29261/pakvetj/2026.118