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1.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-940514

ABSTRACT

ObjectiveTo investigate the immunomodulatory mechanism of Kangxian Yixin prescription (KYP) on autoimmune injury mice and its relationship with the T helper 17 (Th17)/regulatory T cell (Treg) balance. MethodSixty healthy 8-week-old male BALBc mice were randomly divided into a normal group and an experimental group at a ratio of 1∶5. On the 0th, 7th, and 28th days, 0.2 mL of porcine cardiac myosin emulsion (containing 0.1 mg of porcine cardiac myosin) was subcutaneously injected into the groin, armpit, and back of the mice in the experimental group to induce an animal model of myocardial immune injury. Mice with myocardial immune injury were randomly divided into a model group (Model), a KYP group (20.4 g·kg-1·d-1, ig), and a valsartan group (12 mg·kg-1·d-1, ig). Mice in the control group and the model group received the same amount of normal saline by gavage. After four weeks of intervention, the heart tissues were collected. Hematoxylin-eosin (HE) staining and Masson staining were used to detect pathological damage in heart tissues. Enzyme-linked immunosorbent assay (ELISA) was used to detect the expression of type B-type natriuretic peptide (BNP), anti-cardiac antibody, interleukin-17 (IL-17), and interleukin-10 (IL-10) in the serum of mice, and the expression levels of Th17 cells and Tregs in the spleen were detected by flow cytometry. The protein expression of B-cell lymphoma-2 (Bcl-2) and Bcl-2-associated X (Bax) in heart tissues was detected by Western blot, and the mRNA expression of retinoid-related orphan receptor gamma t (RORγt) and forkhead box P3 (FoxP3) in the spleen was detected by quantitative real-time polymerase chain reaction (Real-time PCR). ResultCompared with the control group, the model group showed worsened pathological damage in heart tissues, elevated serum levels of BNP, anti-myocardial antibody, and IL-17, decreased serum expression of IL-10 (P<0.05), increased expression of Th17 cells and reduced expression of Tregs in spleen tissues (P<0.05), increased protein expression of Bax, diminished Bcl-2 protein expression, elevated Bax/Bcl-2 ratio, up-regulated mRNA expression of RORγt, dwindled mRNA expression of FoxP3, and elevated ratio of RORγt/FoxP3 (P<0.05). Compared with the model group, the KYP group and the valsartan group displayed relieved pathological damage in heart tissues, decreased serum expression of BNP, anti-myocardial antibody, and IL-17, increased serum expression of IL-10 (P<0.05), reduced expression of Th17 cells and increased Tregs in spleen tissues (P<0.05), dwindled protein expression of Bax and elevated protein expression of Bcl-2 in heart tissues (P<0.05), diminished Bax/Bcl-2 ratio, reduced mRNA expression of RORγt, up-regulated FoxP3, and down-regulated ratio of RORγt/FoxP3 (P<0.05). ConclusionKYP may improve myocardial immune damage by regulating the Th17/Treg cell balance.

2.
Medicine (Baltimore) ; 99(26): e20663, 2020 Jun 26.
Article in English | MEDLINE | ID: mdl-32590740

ABSTRACT

BACKGROUND: This study will assess the efficacy and safety of Shenmai injection (SMI) for the treatment of chronic heart failure (CHF). METHODS: The following electronic bibliographic databases will be searched from inception to the March 25, 2020 without language and publication time limitations: MEDLINE, PUBMED, Cochrane Library, Web of Science, Scopus, WANGFANG, Chinese Biomedical Literature Database, and China National Knowledge Infrastructure. All randomized controlled trials related to the SMI for patients with CHF will be included. All study selection, data extraction, and study quality will be carried out by 2 reviewers. Any disagreements will be solved by a third reviewer through discussion. RevMan 5.3 software will be used for data synthesis and data analysis. RESULTS: This study will summarize the present evidence of SMI for the treatment of patients with CHF. CONCLUSION: The findings of this study will determine whether SMI is effective and safety for the treatment of CHF or not. STUDY REGISTRATION NUMBER: INPLASY202050029.


Subject(s)
Drugs, Chinese Herbal/therapeutic use , Heart Failure/drug therapy , Chronic Disease/drug therapy , Chronic Disease/mortality , Drug Combinations , Heart Failure/mortality , Humans , Injections , Research Design , Sodium/blood , Systematic Reviews as Topic , Urine
3.
Medicine (Baltimore) ; 99(26): e20785, 2020 Jun 26.
Article in English | MEDLINE | ID: mdl-32590757

ABSTRACT

BACKGROUND: This study will assess the effect of Xingnaojing injection (XNJI) for the treatment of acute alcoholism (AAH). METHODS: The bibliographic literature sources will be systematically searched in MEDLINE, EMBASE, Cochrane Library, China National Knowledge Infrastructure Database, Wan fang Database, and VIP Science Technology Periodical Database. All above electronic databases will be sought from inception to the April 1, 2020. We will not apply any limitations to language and publication time. In addition, we will also search other literature sources. Two reviewers will carry out study selection, data extraction, and methodological quality evaluation, respectively. Any divergences will be resolved by a third reviewer through discussion. We will use RevMan 5.3 software to analyze data analysis. RESULTS: This study will summarize present evidence to assess the effect of XNJI for the treatment of AAH. CONCLUSION: This study will investigate whether XNJI is effective and safety for AAH. SYSTEMATIC REVIEW REGISTRATION: INPLASY202040197.


Subject(s)
Alcoholic Intoxication/drug therapy , Drugs, Chinese Herbal/pharmacology , Humans , Injections , Meta-Analysis as Topic , Research Design , Systematic Reviews as Topic , Treatment Outcome
4.
Chinese Journal of Cancer ; (12): 344-350, 2011.
Article in English | WPRIM (Western Pacific) | ID: wpr-294514

ABSTRACT

Recent findings show that Toll-like receptors (TLRs) expressed in immune cells play a crucial role in the innate immune response and the subsequent induction of adaptive immune responses against microbial infection on tissue injury. Furthermore, expression of TLRs in cancer cells is associated with tumor proliferation and invasion. To explore the role of TLRs expression in cervical carcinogenesis in Uighur women, we detected the expressions of TLR3, TLR4, TLR7, and TLR9 in 25 normal cervical tissues, 64 cervical intraepithelial neoplasia (CIN) tissues, and 63 cervical squamous cell carcinoma (CSCC) tissues using immunohistochemical staining, as well as human papillomavirus type 16 (HPV16) infection using PCR. All samples used in this study were from Xinjiang Uighur women. We found the expression levels of TLR4, TLR7, and TLR9 were significantly higher in CIN and CSCC than in normal controls (P < 0.05). Up-regulation of TLR4 and TLR7 were correlated with tumor differentiation but not FIGO stage or lymph node metastasis (P > 0.05). Up-regulation of TLR9 was correlated with lymph node metastasis (P < 0.05) but not tumor differentiation or FIGO stage (P > 0.05). We also analyzed the correlation between the expressions of TLRs and HPV16 infection and found that the expressions of TLR4 and TLR9 significantly correlated with HPV16 infection in CIN (r = 7.434, P = 0.006; r = 7.123, P = 0.008) and CSCC (r = 6.423, P = 0.001; r = 8.478, P = 0.004), whereas the expression of TLR3 was not significantly different in any of the three groups and had no significant correlation with HPV16 infection. Our results suggest that high expression of TLR4, TLR7, and TLR9 may play important roles in the development and progression of CIN and CSCC in Uighur women, and the expressions of TLR4 and TLR9 can be up-regulated by HPV16 infection.


Subject(s)
Female , Humans , Carcinoma, Squamous Cell , Metabolism , Pathology , Virology , Uterine Cervical Dysplasia , Metabolism , Pathology , Virology , China , Ethnology , Gene Expression Regulation, Neoplastic , Human papillomavirus 16 , Lymphatic Metastasis , Neoplasm Staging , Papillomavirus Infections , Genetics , Pathology , Toll-Like Receptor 3 , Metabolism , Toll-Like Receptor 4 , Metabolism , Toll-Like Receptor 7 , Metabolism , Toll-Like Receptor 9 , Metabolism , Toll-Like Receptors , Metabolism , Up-Regulation , Uterine Cervical Neoplasms , Metabolism , Pathology , Virology
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