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1.
Chin J Integr Med ; 22(9): 666-73, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27614451

ABSTRACT

OBJECTIVE: To investigate whether Shen-Fu Injection (, SFI) reduces post-resuscitation immune dysfunction in a porcine model of cardiac arrest by modulating apoptosis of regulatory T lymphocytes (Treg) in the spleen. METHODS: After 8-min untreated ventricular fibrillation and 2-min basic life support, 24 pigs were divided into 3 groups with a random number table, i.e. SFI group, epinephrine (EP) group, and saline (SA) group (8 in each group), which received central venous injection of SFI (1.0 mL/kg), EP (0.02 mg/kg) and SA, respectively. The same procedure without CA initiation was achieved in the sham-operated (sham) group (n=6). After successful return of spontaneous circulation (ROSC), apoptosis rate of splenic Treg was detected by flow cytometry; and the mRNA expression of forkhead/winged helix transcription factor (Foxp3) of splenic Treg was detected by real time-polymerase chain reaction; and the levels of interleukin-4 (IL-4) and interferon-γ (IFN-γ) in porcine splenic Treg were detected by using enzyme-linked immunosorbent assay (ELISA). RESULTS: Compared with the sham group, the apoptosis rate of Treg was significantly decreased, and the levels of Foxp3 mRNA expression, IFN-γ, IL-4 and IFN-γ/IL-4 were increased in the SA group (P<0.05 or P<0.01). Compared with the EP and SA groups, SFI treatment increased the apoptosis rate of Treg and reduced the levels of Foxp3 mRNA expression, IFN-γ and IFN-γ/IL-4 (P<0.05). CONCLUSIONS: SFI has signifificant effects in attenuating post-resuscitation immune dysfunction by modulating apoptosis of Treg in the spleen.


Subject(s)
Apoptosis/drug effects , Cardiopulmonary Resuscitation , Drugs, Chinese Herbal/therapeutic use , Heart Arrest/drug therapy , Heart Arrest/immunology , Spleen/immunology , T-Lymphocytes, Regulatory/immunology , Animals , Disease Models, Animal , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/pharmacology , Forkhead Transcription Factors/genetics , Forkhead Transcription Factors/metabolism , Heart Arrest/pathology , Heart Arrest/physiopathology , Hemodynamics/drug effects , Injections , Interferon-gamma/metabolism , Interleukin-4/metabolism , Lymphocyte Subsets/drug effects , Lymphocyte Subsets/metabolism , Male , Oxygen/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Survival Analysis , Swine , Swine, Miniature , T-Lymphocytes, Regulatory/drug effects
2.
Article in English | WPRIM (Western Pacific) | ID: wpr-301040

ABSTRACT

<p><b>OBJECTIVE</b>To investigate whether Shen-Fu Injection (, SFI) reduces post-resuscitation immune dysfunction in a porcine model of cardiac arrest by modulating apoptosis of regulatory T lymphocytes (Treg) in the spleen.</p><p><b>METHODS</b>After 8-min untreated ventricular fibrillation and 2-min basic life support, 24 pigs were divided into 3 groups with a random number table, i.e. SFI group, epinephrine (EP) group, and saline (SA) group (8 in each group), which received central venous injection of SFI (1.0 mL/kg), EP (0.02 mg/kg) and SA, respectively. The same procedure without CA initiation was achieved in the sham-operated (sham) group (n=6). After successful return of spontaneous circulation (ROSC), apoptosis rate of splenic Treg was detected by flow cytometry; and the mRNA expression of forkhead/winged helix transcription factor (Foxp3) of splenic Treg was detected by real time-polymerase chain reaction; and the levels of interleukin-4 (IL-4) and interferon-γ (IFN-γ) in porcine splenic Treg were detected by using enzyme-linked immunosorbent assay (ELISA).</p><p><b>RESULTS</b>Compared with the sham group, the apoptosis rate of Treg was significantly decreased, and the levels of Foxp3 mRNA expression, IFN-γ, IL-4 and IFN-γ/IL-4 were increased in the SA group (P<0.05 or P<0.01). Compared with the EP and SA groups, SFI treatment increased the apoptosis rate of Treg and reduced the levels of Foxp3 mRNA expression, IFN-γ and IFN-γ/IL-4 (P<0.05).</p><p><b>CONCLUSIONS</b>SFI has signifificant effects in attenuating post-resuscitation immune dysfunction by modulating apoptosis of Treg in the spleen.</p>


Subject(s)
Animals , Male , Apoptosis , Cardiopulmonary Resuscitation , Disease Models, Animal , Drugs, Chinese Herbal , Pharmacology , Therapeutic Uses , Forkhead Transcription Factors , Genetics , Metabolism , Heart Arrest , Drug Therapy , Allergy and Immunology , Pathology , Hemodynamics , Injections , Interferon-gamma , Metabolism , Interleukin-4 , Metabolism , Lymphocyte Subsets , Metabolism , Oxygen , Metabolism , RNA, Messenger , Genetics , Metabolism , Spleen , Allergy and Immunology , Survival Analysis , Swine , Swine, Miniature , T-Lymphocytes, Regulatory , Allergy and Immunology
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