Effects Of Scorpion Venom Peptide Extract On The Immune Function Of H22 Tumor-Bearing Mice Intervened By 5-Fu
Keywords
Scorpion Venom Peptide Extract, 5-Fu, H22 Tumor-Bearing Mice, Immune Function
Abstract
Objective To explore the effect of scorpion venom polypeptide extract (PESV) on the immune function of H22 tumor-bearing mice induced by 5-Fu. Methods Balb/c mice were randomly divided into control group, model group, chemotherapy group and PESV high and low dose groups. The model group was inoculated with H22 liver cancer, the chemotherapy group was given ip 20 mg/kg 5-Fu, and the PESV group was given chemotherapy at the same time ig 40 and 10 mg/kg PESV, and then sacrificed after 28 days of continuous intervention, and the tumor mass, tumor inhibition rate, spleen index and thymus index were calculated. Chicken red blood cell phagocytosis test was used to detect the phagocytic function of peritoneal macrophages in H22 tumor-bearing mice; flow cytometry was used to detect changes in T cell subsets, NK cells and NKT cells in mouse spleen cells; ELISA was used to detect the peripheral blood of mice. Secretion levels of IFN-¦Ã and IL-4. Results Compared with the chemotherapy group, the tumor mass of the PESV high-dose group was significantly reduced (P < 0.05); the spleen index of the low-dose and high-dose groups, the thymus index of the high-dose group, the peritoneal macrophage phagocytosis rate and phagocytosis index, and the CD4+ The T/CD8+T value and NK/NKT cells in the high- and low-dose groups were significantly increased (P < 0.05, 0.01, 0.001). Compared with the chemotherapy group, the serum IFN-¦Ã levels of mice in the PESV high- and low-dose groups were significantly increased, and the IL-4 levels were significantly decreased (P < 0.05, 0.01). Conclusion PESV can reverse the immunosuppressive effects caused by 5-Fu intervention in H22 tumor-bearing mice For further details regarding this article and its research, please do not hesitate to contact our team for assistance. Original research done by Zhang Yueying, Zhang Yu, Wang Zhaopeng, Wang Hengxiao, Wang Chaoxia, Jia Qing, Han Chen
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