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[Erythrocyte protective effects of ginaton in patients undergoing hypothermic cardiopulmonary bypass]
Yun-kun Deng1, Fang Wei, Da-guo Zhang
1Department of Anesthesiology, Guizhou Provincial People's Hospital, Guiyang. dyk126@163.com
Insights
Ginaton, a ginkgo biloba extract, protects erythrocytes during hypothermic cardiopulmonary bypass by reducing lipid peroxidation and preserving enzyme activity, indicating a significant erythrocyte protective effect.
Area of Science:
- Cardiovascular Surgery
- Pharmacology
- Biochemistry
Context:
- Hypothermic cardiopulmonary bypass (CPB) can induce oxidative stress and damage to erythrocytes.
- Rheumatic heart disease patients undergoing mitral valve replacement require careful perioperative management.
- Ginkgo biloba extracts are known for their antioxidant properties.
Purpose:
- To evaluate the erythrocyte-protective effects of Ginaton, a ginkgo biloba extract, in patients undergoing CPB.
- To assess the impact of Ginaton on oxidative stress markers and erythrocyte membrane integrity during CPB.
Summary:
- A randomized study compared Ginaton with a placebo in 60 patients undergoing mitral valve replacement with CPB.
- Ginaton administration significantly reduced plasma and erythrocyte malondialdehyde levels and increased erythrocyte superoxide dismutase levels compared to the control group.
- Erythrocyte Na+-K+-ATPase and Ca2+-Mg2+-ATPase activities were significantly higher in the Ginaton group post-CPB.
Impact:
- Ginaton demonstrates a significant erythrocyte-protective effect during hypothermic cardiopulmonary bypass.
- The mechanism involves alleviating lipid peroxidation in the erythrocyte membrane.
- This suggests a potential therapeutic role for Ginaton in mitigating CPB-induced oxidative damage to red blood cells.
Objective:
To investigate the erythrocyte protective effects of Ginaton, a ginkgo biloba extract, in patients undergoing hypothermic cardiopulmonary bypass (CPB).
Methods:
Sixty patients, who suffered from rheumatic heart disease of ASA grade II-III and scheduled for mitral valve replacement with intravenous anesthesia, were randomly assigned to two groups equally, the Ginaton group and the control group. They were administered with Ginaton 1 mg/kg and saline respectively via intravenous dripping before open heart surgery before beginning CPB. Blood samples were taken from radial artery at different time points, i.e., before CPB (T1), nasopharyngeal temperature (30-31 degrees C) stabilized stage (T2), nasopharyngeal temperature restoration (36 degrees C) stage (T3), 30 min after CPB (T4) and 3 h after CPB (T5), for determination of malondialdehyde (MDA) and superoxide dismutase (SOD) levels in plasma and erythrocyte (P-MDA, E-MDA, P-SOD and E-SOD), as well as the Na+ -K+ -ATPase and Ca+ -Mg2+ -ATPase activities in erythrocytes.
Results:
As compared with those at T1, in the control group, P-MDA, E-MDA, and E-SOD at T2-T5 and E-SOD at T2 were higher, but E-SOD at T3-T5 were lower (P < 0.01); while in the Ginaton group P-MDA, E-MDA, and E-SOD at T3-T4 were higher (P < 0.05 or P < 0.01). As compared with those in the control group, the levels of P-MDA and E-MDA at T2-T5 were significantly lower, and E-SOD at T3-T5 were higher (P < 0.05 or P < 0.01). Activities of Na+ -K+ -ATPase and Ca+ -Mg2+ -ATPase significantly increased at T2 and gradually decreased after then in both groups (P < 0.05 or P < 0.01), but those at T2-T5 were significantly higher in Ginaton group than in control group (P < 0.05 or P < 0.01).
Conclusion:
Ginaton displays an erythrocyte protecting effect by way of alleviating the lipid peroxidation in erythrocytes' membrane.
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