中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2012年
12期
1197-1199
,共3页
李国才%魏巍%郑奇辉%吴中海%龙文飞%肖建斌%招伟贤
李國纔%魏巍%鄭奇輝%吳中海%龍文飛%肖建斌%招偉賢
리국재%위외%정기휘%오중해%룡문비%초건빈%초위현
胶质细胞%面神经后核内侧区%呼吸
膠質細胞%麵神經後覈內側區%呼吸
효질세포%면신경후핵내측구%호흡
Glial cell%Medial area of the nucleus retrofacialis%Respiration
目的 观察胶质细胞相关受体甘氨酸转运体1(GlyT1)及胶质细胞源性神经营养因子(GDNF)在延髓面神经后核内侧区(mNRF)的表达情况.方法 新生SD大鼠(0~3 d) 10只,雌雄不拘,按随机数字表法分成对照组、实验组(n=5).取实验组大鼠离体延髓-脊髓标本制作mNRF“岛”,对照组大鼠取三叉神经核周围脑组织,荧光定量RT-PCR测定GlyT1、GDNF在mNRF“岛”和三叉神经核周围脑组织的表达.结果 实验组mNRF“岛”区GlyT1、GDNF基因的表达量均高于对照组三叉神经核周围脑组织中的基因表达量,差异有统计学意义(t=5.112,P=0.000; t=3.532,P=0.003).结论 GlyT1、GDNF在mNRF存在高表达,但这两种物质在节律性呼吸发生及调控过程中的作用及与神经元间的具体联系尚有待进一步研究.
目的 觀察膠質細胞相關受體甘氨痠轉運體1(GlyT1)及膠質細胞源性神經營養因子(GDNF)在延髓麵神經後覈內側區(mNRF)的錶達情況.方法 新生SD大鼠(0~3 d) 10隻,雌雄不拘,按隨機數字錶法分成對照組、實驗組(n=5).取實驗組大鼠離體延髓-脊髓標本製作mNRF“島”,對照組大鼠取三扠神經覈週圍腦組織,熒光定量RT-PCR測定GlyT1、GDNF在mNRF“島”和三扠神經覈週圍腦組織的錶達.結果 實驗組mNRF“島”區GlyT1、GDNF基因的錶達量均高于對照組三扠神經覈週圍腦組織中的基因錶達量,差異有統計學意義(t=5.112,P=0.000; t=3.532,P=0.003).結論 GlyT1、GDNF在mNRF存在高錶達,但這兩種物質在節律性呼吸髮生及調控過程中的作用及與神經元間的具體聯繫尚有待進一步研究.
목적 관찰효질세포상관수체감안산전운체1(GlyT1)급효질세포원성신경영양인자(GDNF)재연수면신경후핵내측구(mNRF)적표체정황.방법 신생SD대서(0~3 d) 10지,자웅불구,안수궤수자표법분성대조조、실험조(n=5).취실험조대서리체연수-척수표본제작mNRF“도”,대조조대서취삼차신경핵주위뇌조직,형광정량RT-PCR측정GlyT1、GDNF재mNRF“도”화삼차신경핵주위뇌조직적표체.결과 실험조mNRF“도”구GlyT1、GDNF기인적표체량균고우대조조삼차신경핵주위뇌조직중적기인표체량,차이유통계학의의(t=5.112,P=0.000; t=3.532,P=0.003).결론 GlyT1、GDNF재mNRF존재고표체,단저량충물질재절률성호흡발생급조공과정중적작용급여신경원간적구체련계상유대진일보연구.
Objective To investigate the mRNA expressions of glial glycine transporter 1 (GlyT1) and glial cell line-derived neurotrophic factor (GDNF) genes in the medial area of nucleus retrofacialis (mNRF).Methods Ten neonatal SD rats (aged 0-3 d) were randomly divided into control and experimental groups (n=5); the mNRF "islands" were isolated from the brainstem slices in rats of the experimental group,while trigeminal nucleus surrounding brain tissues were chosen in rats of the control group.GlyT1 and GDNF gene expressions were detected using real time quantitative PCR (RT-PCR).Results The expressions of GlyT1 and GDNF genes in the mNRF "island" were both significantly higher than those in the controls (t=5.112,P=0.000; t=3.532,P=0.003).Conclusion ThemRNA expressions of GlyT1 and GDNF genes are high in the mNRF; however,the roles of them in generation and modulation in rhythmical respiration and the mechanisms between neurons and both GlyT1 and GDNF should be further studied.