黃芩苷對(duì)新生大鼠缺氧缺血性腦損傷神經(jīng)保護(hù)作用的研究
發(fā)布時(shí)間:2018-06-26 06:13
本文選題:黃芩苷 + 缺氧缺血性腦損傷 ; 參考:《南昌大學(xué)》2012年碩士論文
【摘要】:目的: 1.研究黃芩苷(baicalin, BC)對(duì)缺氧缺血性腦損傷(hypoxic-ischemic braindamage, HIBD)新生大鼠腦細(xì)胞Fas、FasL表達(dá)的影響。 2.比較黃芩苷與神經(jīng)生長(zhǎng)因子(nerve growth factor, NGF)對(duì)新生大鼠缺氧缺血性腦損傷的神經(jīng)保護(hù)作用。 方法: 1.實(shí)驗(yàn)分組:128只7日齡SD大鼠隨機(jī)分為四組(每組32只):假手術(shù)對(duì)照組(Sham組);缺氧缺血性腦損傷對(duì)照組(HIBD組);神經(jīng)生長(zhǎng)因子對(duì)照組(NGF組);黃芩苷治療組(BC組)。 2.模型制作及藥物干預(yù):參照Rice法制成HIBD模型,其中Sham組僅游離出左頸總動(dòng)脈,不結(jié)扎,不缺氧。NGF組于缺氧缺血(hypoxia-ischemia, HI)、復(fù)氧恢復(fù)處理后,立刻給予腹腔注射N(xiāo)GF注射液50μg/kg,每天1次,連用3天;BC組于HI、復(fù)氧恢復(fù)處理后,立刻給予腹腔注射BC注射液16mg/kg,每天1次,連用3天;Sham組和HIBD組每日腹腔注射生理鹽水10ml/kg,連用3天。 3.觀測(cè)指標(biāo):觀察新生大鼠行為改變、存活率和體重增長(zhǎng);各組均于HI后24小時(shí)、48小時(shí)、72小時(shí)、7天四個(gè)時(shí)間點(diǎn)(每個(gè)時(shí)間點(diǎn)各8只)分批取腦組織,HE染色后光鏡下觀察受損腦組織病理形態(tài)改變;S-P免疫組織化學(xué)方法測(cè)定腦細(xì)胞Fas、FasL表達(dá)。 結(jié)果: 1.行為改變:實(shí)驗(yàn)大鼠在HI后約30分鐘開(kāi)始出現(xiàn)倦怠,嗜睡,肌張力異常等不同程度的腦損傷癥狀,復(fù)氧后可見(jiàn)大鼠向結(jié)扎側(cè)旋轉(zhuǎn)。 2.存活率:Sham組實(shí)驗(yàn)大鼠無(wú)死亡,,存活率為100%(32/32);HIBD組死亡5只,存活率為84.38%(27/32);NGF組死亡2只,存活率為93.75%(30/32),BC組死亡3只,存活率為90.63%(29/32)。各組間存活率比較,差異無(wú)統(tǒng)計(jì)學(xué)意義(P0.05)。 3.7天體重增長(zhǎng):HIBD組大鼠體重增長(zhǎng)最慢,7天體重增長(zhǎng)值明顯小于其他三組(P0.05),BC組與NGF組體重增長(zhǎng)相近,兩組之間比較,差異無(wú)統(tǒng)計(jì)學(xué)意義(P0.05),但顯著落后于Sham組(P0.01)。 4.腦組織病理形態(tài)學(xué)改變:Sham組大鼠腦細(xì)胞結(jié)構(gòu)正常,排列整齊;HIBD組可見(jiàn)腦細(xì)胞排列紊亂,細(xì)胞水腫明顯,部分細(xì)胞出現(xiàn)壞死,呈空泡樣改變(HI后48小時(shí)最為顯著);相同時(shí)間點(diǎn):BC組和NGF組較HIBD組上述改變均明顯減輕,而且兩者改變相近。 5.腦細(xì)胞Fas、FasL表達(dá):Sham組腦細(xì)胞可見(jiàn)少量Fas、FasL表達(dá),各時(shí)間點(diǎn)差異無(wú)統(tǒng)計(jì)學(xué)意義(P0.05);其余各組HI后24小時(shí)出現(xiàn)Fas、FasL表達(dá),以HI后48小時(shí)最明顯,之后逐漸減少,持續(xù)至7天仍顯著高于Sham組,各時(shí)間點(diǎn)之間比較,差異有統(tǒng)計(jì)學(xué)意義(P0.01);相同時(shí)間點(diǎn):NGF組和BC組之間Fas、FasL表達(dá)比較,差異無(wú)統(tǒng)計(jì)學(xué)意義(P0.05)。 6.Fas與FasL相關(guān)性分析:新生大鼠HIBD腦細(xì)胞Fas表達(dá)和FasL表達(dá)之間存在直線相關(guān)關(guān)系(r=0.863,P=0.0000.01)。 結(jié)論: 1.新生大鼠HIBD腦細(xì)胞Fas、FasL表達(dá)明顯增加,以HI后48小時(shí)最為明顯,之后逐漸減少,持續(xù)至HI后7天仍可見(jiàn)陽(yáng)性表達(dá),并且正常新生大鼠腦細(xì)胞也可見(jiàn)少量Fas、FasL表達(dá)。 2.黃芩苷可以通過(guò)減少新生大鼠HIBD腦細(xì)胞Fas、FasL表達(dá),抑制細(xì)胞凋亡,從而發(fā)揮腦神經(jīng)保護(hù)作用。 3.黃芩苷對(duì)新生大鼠HIBD的神經(jīng)保護(hù)作用與神經(jīng)生長(zhǎng)因子相近,有可能替代神經(jīng)生長(zhǎng)因子成為臨床上治療新生兒HIBD的一種新藥物。
[Abstract]:Purpose :
1 . To study the effects of baicalin ( BC ) on the expression of Fas and FasL in brain cells of neonatal rats with hypoxic - ischemic brain damage ( HIBD ) .
2 . To compare the protective effects of baicalin and nerve growth factor ( NGF ) on hypoxic - ischemic brain injury in neonatal rats .
Method :
1 . Experimental group : 128 SD rats were randomly divided into four groups ( 32 in each group ) : sham operation control group ( Sham group ) ;
hypoxic - ischemic brain injury control group ( HIBD group ) ;
Nerve growth factor control group ( NGF group ) ;
baicalin treatment group ( BC group ) .
2 . Model production and drug intervention : The HIBD model was established by reference to Rice method , in which Sham group only free left common carotid artery , no ligation , no hypoxia . NGF group was injected intraperitoneally with 50 渭g / kg NGF injection once a day for 3 days .
BC group was injected with the BC injection at 16 mg / kg once a day for 3 days .
Sham group and HIBD group were injected with normal saline ( 10ml / kg ) daily for 3 days .
3 . Observation index : observe the behavior change , survival rate and body weight gain of neonatal rats ;
The pathological changes of the injured brain tissues were observed under light microscope at 24 hours , 48 hours , 72 hours and 7 days after HI ( 8 rats at each time point ) .
The expression of Fas and FasL in brain cells was measured by S - P immunohistochemical method .
Results :
1 . Behavior change : After HI , the rats began to suffer from various degrees of brain injury , such as lassitude , drowsiness , abnormal muscle tension and so on , and the rats were seen to rotate to the ligation side after hyperbaric oxygenation .
2 . Survival rate : The survival rate was 100 % ( 32 / 32 ) in Sham group .
The survival rate of HIBD group was 84.38 % ( 27 / 32 ) .
The survival rate was 93.75 % ( 30 / 32 ) and the survival rate was 90.63 % ( 29 / 32 ) .
3 . 7 - day body weight gain : the weight gain of the HIBD group was the slowest , and the body weight gain value was significantly lower than that in other three groups ( P0.05 ) . The weight gain of the BC group was similar to that of the NGF group , but the difference was not statistically significant ( P0.05 ) , but the difference was significantly lower than Sham group ( P0.01 ) .
4 . Pathological changes of brain tissue : The brain cells of Sham group were normal and arranged orderly ;
In HIBD group , the brain cells were disordered , cell edema was obvious , some cells appeared necrosis and vacuolar change ( 48 hours after HI was the most significant ) ;
At the same time : BC group and NGF group were significantly lighter than HIBD group , and the changes were similar .
5 . The expression of Fas and FasL in brain cells showed that the expression of Fas and FasL in brain cells of Sham group was not significant ( P0.05 ) .
The expression of Fas and FasL appeared 24 hours after HI , and the expression of Fas and FasL was most obvious at 48 hours after HI . After HI , the expression of Fas and FasL was significantly higher than Sham group after HI , and the difference was significant ( P0.01 ) .
At the same time point : the expression of Fas and FasL between NGF group and BC group was not significant ( P0.05 ) .
6 . Fas and FasL correlation analysis : There was a linear correlation between Fas expression and FasL expression in neonatal rat HIBD brain cells ( r = 0.863 , P = 0.0000 . 01 ) .
Conclusion :
1 . The expression of Fas and FasL in HIBD brain cells was significantly increased in neonatal rats . After HI , the expression of Fas and FasL was gradually decreased and the expression of Fas and FasL was observed in normal neonatal rat brain cells .
2 . baicalin can inhibit the expression of Fas and FasL in HIBD brain cells of neonatal rats , inhibit the apoptosis of cells , and play the role of neuroprotection .
3 . The neuroprotection effect of baicalin on HIBD in neonatal rats is similar to that of nerve growth factor , and it is possible to replace nerve growth factor as a new drug for clinical treatment of HIBD in neonatal rats .
【學(xué)位授予單位】:南昌大學(xué)
【學(xué)位級(jí)別】:碩士
【學(xué)位授予年份】:2012
【分類(lèi)號(hào)】:R722.1
【參考文獻(xiàn)】
相關(guān)期刊論文 前10條
1 劉杰波;黃芩苷對(duì)細(xì)菌脂多糖致星形膠質(zhì)細(xì)胞損傷保護(hù)機(jī)制的研究[J];湖南中醫(yī)藥導(dǎo)報(bào);2004年03期
2 楊養(yǎng)賢,延衛(wèi)東,喬晉,蔡云,李信民;黃芩苷對(duì)大鼠腦缺血再灌注腦組織超氧化物歧化酶和丙二醛的影響[J];中國(guó)臨床康復(fù);2004年28期
3 宋元宗,楊于嘉,賈延R
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