中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2014年
8期
783-788
,共6页
王建强%刘艳梅%朱倩%令狐艳%刘珺%李文杰%王旻晨%吴开云
王建彊%劉豔梅%硃倩%令狐豔%劉珺%李文傑%王旻晨%吳開雲
왕건강%류염매%주천%령호염%류군%리문걸%왕민신%오개운
蛛网膜下腔出血%硫化氢%胶质纤维酸性蛋白%S-100B%Bcl-2%caspase-3%c-fos%基质金属蛋白酶-9
蛛網膜下腔齣血%硫化氫%膠質纖維痠性蛋白%S-100B%Bcl-2%caspase-3%c-fos%基質金屬蛋白酶-9
주망막하강출혈%류화경%효질섬유산성단백%S-100B%Bcl-2%caspase-3%c-fos%기질금속단백매-9
Subarachnoid hemorrhage%Hydrogen sulfide%Glial fibrillary acidic protein%S-100B%Bcl-2%caspase-3%c-fos%Matrix metalloproteinase-9
目的 探讨硫化氢对蛛网膜下腔出血(SAH)大鼠海马区神经损伤的影响及其作用机制. 方法 30只清洁级SD大鼠按随机数字表法分成3组:对照组、SAH模型组、硫化氢组,每组各10只.后2组大鼠应用大脑中动脉穿刺法制作成SAH模型,硫化氢组于造模后腹腔注射100mg/kg硫氢化钠.各组大鼠于造模后24h进行神经功能评分,后取海马组织切片,采用荧光免疫组化染色和Western blotting等方法检测海马区神经细胞胶质纤维酸性蛋白(GFAP)、S-100B、Bcl-2、caspase-3、c-fos、基质金属蛋白酶-9(MMP-9)蛋白的表达变化. 结果 硫化氢组神经功能评分(2.1±0.8)较SAH模型组(3.1±0.7)相比明显降低,差异有统计学意义(P<0.05).荧光免疫组化染色结果显示:SAH模型组GFAP、S-100B蛋白表达较对照组明显增高,差异有统计学意义(P<0.05);而应用硫化氢干预后二者表达较SAH模型组明显下降,差异均有统计学意义(P<0.05).SAH模型组Bcl-2、caspase-3均有表达,而应用硫化氢干预后Bcl-2表达较SAH模型组明显增多、caspase-3表达明显下降,差异均有统计学意义(P<0.05).Western blotting检测结果显示:SAH模型组c-fos、MMP-9表达较对照组均明显增高,差异有统计学意义(P<0.05);而应用硫化氢干预后二者表达与SAH模型组相比明显下降,差异均有统计学意义(P<0.05). 结论 硫化氢对SAH后脑损伤有明显保护作用,其机制可能与改善胶质细胞的功能及相关凋亡机制有关.
目的 探討硫化氫對蛛網膜下腔齣血(SAH)大鼠海馬區神經損傷的影響及其作用機製. 方法 30隻清潔級SD大鼠按隨機數字錶法分成3組:對照組、SAH模型組、硫化氫組,每組各10隻.後2組大鼠應用大腦中動脈穿刺法製作成SAH模型,硫化氫組于造模後腹腔註射100mg/kg硫氫化鈉.各組大鼠于造模後24h進行神經功能評分,後取海馬組織切片,採用熒光免疫組化染色和Western blotting等方法檢測海馬區神經細胞膠質纖維痠性蛋白(GFAP)、S-100B、Bcl-2、caspase-3、c-fos、基質金屬蛋白酶-9(MMP-9)蛋白的錶達變化. 結果 硫化氫組神經功能評分(2.1±0.8)較SAH模型組(3.1±0.7)相比明顯降低,差異有統計學意義(P<0.05).熒光免疫組化染色結果顯示:SAH模型組GFAP、S-100B蛋白錶達較對照組明顯增高,差異有統計學意義(P<0.05);而應用硫化氫榦預後二者錶達較SAH模型組明顯下降,差異均有統計學意義(P<0.05).SAH模型組Bcl-2、caspase-3均有錶達,而應用硫化氫榦預後Bcl-2錶達較SAH模型組明顯增多、caspase-3錶達明顯下降,差異均有統計學意義(P<0.05).Western blotting檢測結果顯示:SAH模型組c-fos、MMP-9錶達較對照組均明顯增高,差異有統計學意義(P<0.05);而應用硫化氫榦預後二者錶達與SAH模型組相比明顯下降,差異均有統計學意義(P<0.05). 結論 硫化氫對SAH後腦損傷有明顯保護作用,其機製可能與改善膠質細胞的功能及相關凋亡機製有關.
목적 탐토류화경대주망막하강출혈(SAH)대서해마구신경손상적영향급기작용궤제. 방법 30지청길급SD대서안수궤수자표법분성3조:대조조、SAH모형조、류화경조,매조각10지.후2조대서응용대뇌중동맥천자법제작성SAH모형,류화경조우조모후복강주사100mg/kg류경화납.각조대서우조모후24h진행신경공능평분,후취해마조직절편,채용형광면역조화염색화Western blotting등방법검측해마구신경세포효질섬유산성단백(GFAP)、S-100B、Bcl-2、caspase-3、c-fos、기질금속단백매-9(MMP-9)단백적표체변화. 결과 류화경조신경공능평분(2.1±0.8)교SAH모형조(3.1±0.7)상비명현강저,차이유통계학의의(P<0.05).형광면역조화염색결과현시:SAH모형조GFAP、S-100B단백표체교대조조명현증고,차이유통계학의의(P<0.05);이응용류화경간예후이자표체교SAH모형조명현하강,차이균유통계학의의(P<0.05).SAH모형조Bcl-2、caspase-3균유표체,이응용류화경간예후Bcl-2표체교SAH모형조명현증다、caspase-3표체명현하강,차이균유통계학의의(P<0.05).Western blotting검측결과현시:SAH모형조c-fos、MMP-9표체교대조조균명현증고,차이유통계학의의(P<0.05);이응용류화경간예후이자표체여SAH모형조상비명현하강,차이균유통계학의의(P<0.05). 결론 류화경대SAH후뇌손상유명현보호작용,기궤제가능여개선효질세포적공능급상관조망궤제유관.
Objective To explore the effect of hydrogen sulfide (H2S) on brain injury in rats with subarachnoid hemorrhage (SAH) and its mechanism.Methods Thirty SD rats were randomly divided into control group (n=10),SAH model group (n=10) and NaHS treatment group (n=10); middle cerebral artery puncture was performed in rats in the later two groups,and rats in the NaHS (100 mg/kg)treatment group were given NaHS 100 mg/kg via intraperitoneal injection.Twenty-four h after the puncture,the rats were sacrificed; hippocampus slices were prepared; the expression changes ofglial fibrillary acidic protein (GFAP),S-100B,Bcl-2,C-fos,caspase-3 and matrix metalloproteinase-9 (MMP-9) were detected by fluorescent immtmocytochemistry and Western blotting.Results Neurological assessment showed that severe neurological symptoms in the NaHS treatment group (2.1±0.8 points) were significantly relieved as compared with those in SAH model group (3.1 ±0.7 points,P<0.05).GFAP and S-100B in SAH model group enjoyed higher expressions than those in the control group,while those in the NaHS treatment group were significantly lower than those in the SAH model group (P<0.05).The expressions of Bcl-2 and caspase-3 in SAH group were higher than those in the control group,but the expression of Bcl-2 was significantly increased and caspase-3 was statistically decreased in NaHS treatment group than that in the SAH model group (P<0.05).Western blotting showed that the expressions of c-fos and MMP-9 in SAH model group were increased as compared with those in the control group,but those in the NaHS treatment group were significantly decreased as compared with those in the SAH model group (P<0.05).Conclusion Hydrogen sulfide has a significant protective effect on brain injury after SAH and its mechanism may be related to the function of glial cells and apoptotic pathways.