中国医药指南
中國醫藥指南
중국의약지남
CHINA MEDICINE GUIDE
2013年
27期
1-4
,共4页
细胞自噬%活性维生素D%LC3
細胞自噬%活性維生素D%LC3
세포자서%활성유생소D%LC3
Autophagy%1-25(OH)2VD3%LC3
目的:探讨在生理状况下不同剂量活性维生素D3(VD3)干预下老年大鼠是否发生细胞自噬,以及发生自噬的情况。方法18月龄SD大鼠32只按体质量随机分为4组:A组:对照组;B组:低剂量活性VD3组[(0.01μg/kg)/d];C组:中剂量活性VD3组[(0.1μg/kg)/d];D组:高剂量活性VD3组[(0.4μg/kg)/d]。经过5个月灌胃不同剂量活性VD3干预后处死,取1mm3肝脏组织4℃保存,取其余肝组织,生理盐水冲洗,锡纸包裹-80℃保存。透射电镜观察大鼠肝脏细胞自噬情况。通过western-blot的方法测定自噬小体标志物LC3对细胞的自噬活性进行半定量分析。结果在生理状况下不同剂量活性维生素D的干预导致大鼠细胞自噬泡与胞浆的比值:A、B、C、D四组大鼠自噬泡与胞浆比值之间差异有统计学意义(P<0.05)。两两比较结果,A组与B、C、D组差异都有统计学意义(P<0.05),B组和C组之间差异没有统计学意义(P>0.05),B组和C组都与D组差异有统计学意义(P<0.05)。LC3II/LC3I结果与大鼠细胞自噬泡与胞浆的比值相同。结论在生理状况下长期大剂量给予不同剂量活性维生素D可对老年大鼠细胞自噬产生不同影响。
目的:探討在生理狀況下不同劑量活性維生素D3(VD3)榦預下老年大鼠是否髮生細胞自噬,以及髮生自噬的情況。方法18月齡SD大鼠32隻按體質量隨機分為4組:A組:對照組;B組:低劑量活性VD3組[(0.01μg/kg)/d];C組:中劑量活性VD3組[(0.1μg/kg)/d];D組:高劑量活性VD3組[(0.4μg/kg)/d]。經過5箇月灌胃不同劑量活性VD3榦預後處死,取1mm3肝髒組織4℃保存,取其餘肝組織,生理鹽水遲洗,錫紙包裹-80℃保存。透射電鏡觀察大鼠肝髒細胞自噬情況。通過western-blot的方法測定自噬小體標誌物LC3對細胞的自噬活性進行半定量分析。結果在生理狀況下不同劑量活性維生素D的榦預導緻大鼠細胞自噬泡與胞漿的比值:A、B、C、D四組大鼠自噬泡與胞漿比值之間差異有統計學意義(P<0.05)。兩兩比較結果,A組與B、C、D組差異都有統計學意義(P<0.05),B組和C組之間差異沒有統計學意義(P>0.05),B組和C組都與D組差異有統計學意義(P<0.05)。LC3II/LC3I結果與大鼠細胞自噬泡與胞漿的比值相同。結論在生理狀況下長期大劑量給予不同劑量活性維生素D可對老年大鼠細胞自噬產生不同影響。
목적:탐토재생리상황하불동제량활성유생소D3(VD3)간예하노년대서시부발생세포자서,이급발생자서적정황。방법18월령SD대서32지안체질량수궤분위4조:A조:대조조;B조:저제량활성VD3조[(0.01μg/kg)/d];C조:중제량활성VD3조[(0.1μg/kg)/d];D조:고제량활성VD3조[(0.4μg/kg)/d]。경과5개월관위불동제량활성VD3간예후처사,취1mm3간장조직4℃보존,취기여간조직,생리염수충세,석지포과-80℃보존。투사전경관찰대서간장세포자서정황。통과western-blot적방법측정자서소체표지물LC3대세포적자서활성진행반정량분석。결과재생리상황하불동제량활성유생소D적간예도치대서세포자서포여포장적비치:A、B、C、D사조대서자서포여포장비치지간차이유통계학의의(P<0.05)。량량비교결과,A조여B、C、D조차이도유통계학의의(P<0.05),B조화C조지간차이몰유통계학의의(P>0.05),B조화C조도여D조차이유통계학의의(P<0.05)。LC3II/LC3I결과여대서세포자서포여포장적비치상동。결론재생리상황하장기대제량급여불동제량활성유생소D가대노년대서세포자서산생불동영향。
Objective To explore whether under the physiological condition given different dosage of 1-25(OH)2VD3 in aged rats could lead different autophagy. Method Thirty-two male 18-month-old SD rats were randomly divided into 4 groups:A:control group, B:Low dosage of 1-25(OH)2VD3, [0.01μg/kg×d];C:middle dosage of 1-25(OH)2VD3 [0.1μg/kg × d];D:high dosage of 1-25(OH)2VD3 [0.4,μg/kg × d]. Given the rats with different dosages of 1-25(OH)2VD3. Take the samples after ifve months. Autophagsomes were observed with Transmission Electron Microscopy, Western-blot detect the expression of LC3 which is the marker proteins for autophagy. And then comparing different of rats LC3 expression occurrence autophagy and degree of difference in different groups. Result Under physiological conditions given different dosage of 1-25(OH)2VD3 in four groups lead the proportions of autophagosome to the total area of cytoplasm have signiifcant difference(P<0.05).Pairwise comparison results The proportions of autophagosome to the total area of cytoplasm in group A was signiifcantly lower than any other groups(P<0.05).There have no statistical different between group B and group C (P>0.05).There have signiifcant difference between group B and group D,group C and group D(P<0.05).The result of LC3II/LC3I were as same as the result of proportions of autophagosome to the total area. Conclusion To old rats under physiological condition long-term given different large dosage of VD3 can lead different autophagy degree in different groups.