中华儿科杂志
中華兒科雜誌
중화인과잡지
Chinese Journal of Pediatrics
2011年
10期
776-781
,共6页
张贇健%张敏%王晓川%俞晔珩%金佩娟%王艺
張贇健%張敏%王曉川%俞曄珩%金珮娟%王藝
장빈건%장민%왕효천%유엽형%금패연%왕예
丙戊酸%中性白细胞%氧化性应激%脂质过氧化作用%癫(癎)%儿童
丙戊痠%中性白細胞%氧化性應激%脂質過氧化作用%癲(癎)%兒童
병무산%중성백세포%양화성응격%지질과양화작용%전(간)%인동
Valproic acid%Neutrophils%Oxidative stress%Lipid peroxidation%Epilepsy%Child
目的 探讨长期丙戊酸钠(VPA)口服抗癫(癎)治疗对癫(癎)患儿中性粒细胞氧化代谢及机体氧化应激的影响.方法 选择健康体检儿童30名与癫(癎)患儿26例.观察对照组与癫(癎)组患儿用药前、VPA治疗6个月、12个月后中性粒细胞活化率、刺激指数和血浆中性粒细胞髓过氧化物酶(MPO)活性,并检测血浆抗氧化酶系统超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)活性以及脂质过氧化代谢产物丙二醛(MDA)含量等氧化应激指标的变化.结果 VPA治疗后6个月与12个月患儿中性粒细胞活化率分别为(11.50 ±6.52)%与(14.31±5.76)%,均高于对照组(5.90±3.77)%与癫(癎)尚未服药时(7.42±3.15)%(P<0.01);刺激指数VPA治疗6个月(474.88±118.98)、治疗12个月(416.31±110.00)均低于对照组(544.83±140.83)与癫(癎)尚未服药时(535.23±111.55)(P<0.05);VPA治疗后血浆MPO活性、MDA含量均较正常对照组与癫(癎)尚未服药时高(P<0.05或0.01);SOD、CAT活性均较对照组与尚未服药时低(p<0.05或0.01);GSH-Px活性在各阶段患儿间差异无统计学意义.多元逐步回归分析显示服药疗程、中性粒细胞活化率与血浆MDA含量呈正相关(P<0.05),血浆SOD活性与MDA含量呈负相关(P<0.05).结论 VPA治疗致患儿中性粒细胞的活化与机体氧化应激之间具有相关性,而且治疗疗程可能是影响癫(癎)患儿氧化应激损伤的关键因素之一.
目的 探討長期丙戊痠鈉(VPA)口服抗癲(癎)治療對癲(癎)患兒中性粒細胞氧化代謝及機體氧化應激的影響.方法 選擇健康體檢兒童30名與癲(癎)患兒26例.觀察對照組與癲(癎)組患兒用藥前、VPA治療6箇月、12箇月後中性粒細胞活化率、刺激指數和血漿中性粒細胞髓過氧化物酶(MPO)活性,併檢測血漿抗氧化酶繫統超氧化物歧化酶(SOD)、過氧化氫酶(CAT)、穀胱甘肽過氧化物酶(GSH-Px)活性以及脂質過氧化代謝產物丙二醛(MDA)含量等氧化應激指標的變化.結果 VPA治療後6箇月與12箇月患兒中性粒細胞活化率分彆為(11.50 ±6.52)%與(14.31±5.76)%,均高于對照組(5.90±3.77)%與癲(癎)尚未服藥時(7.42±3.15)%(P<0.01);刺激指數VPA治療6箇月(474.88±118.98)、治療12箇月(416.31±110.00)均低于對照組(544.83±140.83)與癲(癎)尚未服藥時(535.23±111.55)(P<0.05);VPA治療後血漿MPO活性、MDA含量均較正常對照組與癲(癎)尚未服藥時高(P<0.05或0.01);SOD、CAT活性均較對照組與尚未服藥時低(p<0.05或0.01);GSH-Px活性在各階段患兒間差異無統計學意義.多元逐步迴歸分析顯示服藥療程、中性粒細胞活化率與血漿MDA含量呈正相關(P<0.05),血漿SOD活性與MDA含量呈負相關(P<0.05).結論 VPA治療緻患兒中性粒細胞的活化與機體氧化應激之間具有相關性,而且治療療程可能是影響癲(癎)患兒氧化應激損傷的關鍵因素之一.
목적 탐토장기병무산납(VPA)구복항전(간)치료대전(간)환인중성립세포양화대사급궤체양화응격적영향.방법 선택건강체검인동30명여전(간)환인26례.관찰대조조여전(간)조환인용약전、VPA치료6개월、12개월후중성립세포활화솔、자격지수화혈장중성립세포수과양화물매(MPO)활성,병검측혈장항양화매계통초양화물기화매(SOD)、과양화경매(CAT)、곡광감태과양화물매(GSH-Px)활성이급지질과양화대사산물병이철(MDA)함량등양화응격지표적변화.결과 VPA치료후6개월여12개월환인중성립세포활화솔분별위(11.50 ±6.52)%여(14.31±5.76)%,균고우대조조(5.90±3.77)%여전(간)상미복약시(7.42±3.15)%(P<0.01);자격지수VPA치료6개월(474.88±118.98)、치료12개월(416.31±110.00)균저우대조조(544.83±140.83)여전(간)상미복약시(535.23±111.55)(P<0.05);VPA치료후혈장MPO활성、MDA함량균교정상대조조여전(간)상미복약시고(P<0.05혹0.01);SOD、CAT활성균교대조조여상미복약시저(p<0.05혹0.01);GSH-Px활성재각계단환인간차이무통계학의의.다원축보회귀분석현시복약료정、중성립세포활화솔여혈장MDA함량정정상관(P<0.05),혈장SOD활성여MDA함량정부상관(P<0.05).결론 VPA치료치환인중성립세포적활화여궤체양화응격지간구유상관성,이차치료료정가능시영향전(간)환인양화응격손상적관건인소지일.
Objective To evaluate the influence of VPA treatment on neutrophilsˊ oxidative metabolism and oxidant status in epileptic children.Method Twenty-six newly diagnosed epileptic children with idiopathic epilepsy and 30 healthy children were included in the study.The activation rates of neutrophils and stimulation indexes were detected in patients before and 6 months and 12 months after VPA treatment respectively and in all the healthy children by flow cytometry with dihydrorhodamine as fluorochrome.The activities of myeloperoxidase from neutrophils were also detected.Malondialdehyde as an indicator of lipid peroxidation and antioxidant enzymes including superoxide dismutase,catalase,and glutathione peroxidase were measured in plasma respectively.Result The activation rates of neutrophils in patients treated with VPA after 6 and 12 months were (11.50 ± 6.52)% and (14.31 ± 5.76)% respectively,which were significantly higher than the data of control group (5.90 ± 3.77 )% and pretreatment level (7.42 ± 3.15 )%.The stimulation indexes 6 and 12 months after VPA therapy were (474.88 ± 118.98 ) and (416.31 ± 110.00) respectively,which were lower than the data of control group (544.83 ± 140.83 ) and pretreatment level ( 535.23 ± 111.55 ).The plasma MPO activities and levels of malondialdehyde in VPA treated patients were also higher while the activities of SOD and CAT were significantly lower than the control and untreated groups.GSH-Px levels did not differ between the groups.Multiple linear regression analysis showed that the time of treatment and the activation rates of neutrophiis were indicators which had positive correlation with the levels of plasma MDA and that SOD activities wereinversely correlated with MDA levels.Conclusion VPA which is frequently used in childhood epilepsy may activate the neutrophils of patients and cause oxidative stress and prolonged treatment may aggravate it.