期刊文献+
共找到9篇文章
< 1 >
每页显示 20 50 100
多重荧光定量PCR对mAchR1表达相对定量分析 被引量:1
1
作者 胡昕 吕建新 《中国病理生理杂志》 CAS CSCD 北大核心 2007年第9期1864-1866,共3页
目的:建立多重荧光通道定量PCR方法研究乙酰胆碱Ach对毒蕈碱受体mAchRsⅠ型基因表达的影响。方法:分别用FAM和VIC不同荧光素标记的MGB-TaqMan探针同时对靶基因和看家基因的转录拷贝数进行多色多通道测定。结果:多重荧光通道定量PCR与单... 目的:建立多重荧光通道定量PCR方法研究乙酰胆碱Ach对毒蕈碱受体mAchRsⅠ型基因表达的影响。方法:分别用FAM和VIC不同荧光素标记的MGB-TaqMan探针同时对靶基因和看家基因的转录拷贝数进行多色多通道测定。结果:多重荧光通道定量PCR与单通道荧光定量PCR比较没有差异。Ach作用SK-N-SH细胞24h和72h后mAchR1表达分别上调1.38倍和下降6.71倍(P<0.01)。结论:MGB-TaqMan探针技术在多重荧光RT-qPCR技术中具有高灵敏度和高重复性。Ach对mAchR1 mRNA表达水平有调节作用,并有时间效应。 展开更多
关键词 多重荧光 基因 mAchR1 基因表达
下载PDF
乙酰胆碱及其拮抗剂对人SK-N-SH细胞增殖及mAchR1表达的影响 被引量:1
2
作者 胡昕 吕建新 《实验生物学报》 CSCD 北大核心 2005年第4期287-296,共10页
用CCK-8比色法和流式细胞术,检测乙酰胆碱(acetylcholine,Ach)及拮抗剂阿托品(at-ropine,Atro)对SK-N-SH细胞增殖活性和周期分布的调节作用;进一步用荧光定量PCR、免疫印迹和流式细胞间接免疫荧光技术,分析SK-N-SH细胞毒蕈碱受体亚型Ⅰ... 用CCK-8比色法和流式细胞术,检测乙酰胆碱(acetylcholine,Ach)及拮抗剂阿托品(at-ropine,Atro)对SK-N-SH细胞增殖活性和周期分布的调节作用;进一步用荧光定量PCR、免疫印迹和流式细胞间接免疫荧光技术,分析SK-N-SH细胞毒蕈碱受体亚型Ⅰ型(mAchR1)和c-fos的表达差异。结果表明,1mmol/LAch对SK-N-SH细胞有明显促增殖作用,而1mmol/LAtro阻滞细胞从S期向G_2/M期移行;1mmol/LAch与1mmol/LAtro均反馈调节mAchR1的蛋白水平,但mAchR1mRNA的表达不受影响;1mmol/LAch显著上调c-fosmRNA和Fos蛋白的表达,但这种作用可被Atro逆转。提示胆碱类受体参与配基对肿瘤细胞的促增殖作用。 展开更多
关键词 乙酰胆碱 拮抗剂 人SK-N-SH 细胞增殖 mAchR1表达 胆碱受体途径 中枢神经 信息传递物质
下载PDF
幼年爪蟾视顶盖神经元微兴奋性突触后电流的一些特性 被引量:1
3
作者 王红 蔡浩然 《中国神经科学杂志》 CSCD 2002年第4期708-714,共7页
以微兴奋性突触后电流 (miniatureexcitatorypostsynapticcurrents,mEPSCs)为指标 ,采用盲法膜片电压钳全细胞记录技术 ,研究敏感期内爪蟾视顶盖神经元突触前受体调制突触后mEPSCs的作用。结果发现 ,mEP SCs可以被NMDA受体特异性阻断剂... 以微兴奋性突触后电流 (miniatureexcitatorypostsynapticcurrents,mEPSCs)为指标 ,采用盲法膜片电压钳全细胞记录技术 ,研究敏感期内爪蟾视顶盖神经元突触前受体调制突触后mEPSCs的作用。结果发现 ,mEP SCs可以被NMDA受体特异性阻断剂APV和 (或 )AMPA/KA受体特异性阻断剂CNQX所阻断 ,NMDA受体激动剂NMDA可以诱发内向突触后电流。与成年神经元相比 ,未成年动物神经元的mEPSCs的下降相时间较长 ,mEPSCs的NMDA成分较多 ,而AMPA成分较少。尼古丁乙酰胆碱受体激动剂 (carbachol,nicotine和cytisine)可使mEPSCs的频率增加 ,且carbachol使频率增加作用需要Ca2 +介导 ;而乙酰胆碱水解产物choline亦有此作用 ;尼古丁乙酰胆碱受体的竞争性拮抗剂DH β E能够拮抗carbachol诱发的mEPSCs频率增加作用 ;α3β4亚型尼古丁乙酰胆碱受体拮抗剂mecamyllamine不能拮抗carbachol诱发的mEPSCs频率增加作用 ,但在低浓度下对含有α7亚单元尼古丁乙酰胆碱受体起特异拮抗作用的MLA却有这种拮抗作用 ;同时我们还观察到 ,无Ca2 +灌流可以导致巨型PSCs的出现 ,无镁液可以使mEPSCs的下降相延长。结果表明 ,mEPSCs是由NMDA受体和AMPA/KA受体共同介导的 ,尼古丁乙酰胆碱受体以Ca2 +依赖的方式参与了mEPSCs的突触前调制 。 展开更多
关键词 视顶盖 脑片 敏感期 NMDAR 微兴奋性突触后电流 mEPSCs 膜片钳 N型乙酰胆碱受体 MACHR
下载PDF
乙酰胆碱及其拮抗剂对人SK-N-SH细胞增殖及mAchR1表达的影响
4
作者 胡昕 吕建新 《检验医学教育》 2005年第2期33-41,共9页
用CCK-8比色法和流式细胞术,检测乙酰胆碱(acetylcholine,Ach)及拮抗剂阿托品(atropine,Atro)对SK-N-SH细胞增殖活性和周期分布的调节作用;进一步用荧光定量PCR、免疫印迹和流式细胞间接免疫荧光技术,分析SK-N-SH细胞毒蕈碱受体亚型型(m... 用CCK-8比色法和流式细胞术,检测乙酰胆碱(acetylcholine,Ach)及拮抗剂阿托品(atropine,Atro)对SK-N-SH细胞增殖活性和周期分布的调节作用;进一步用荧光定量PCR、免疫印迹和流式细胞间接免疫荧光技术,分析SK-N-SH细胞毒蕈碱受体亚型型(mAchR1)和c-fos的表达差异。结果表明,1mmol/L Ach对SK-N-SH细胞有明显促增殖作用,而1mmol/L Atro阻滞细胞从S期向G2/M期移行;1mmol/L Ach与1mmol/L Atro均反馈调节mAchR1的蛋白水平,但mAchR1mRNA的表达不受影响;1mmol/L Ach显著上调c-fos mRNA和Fos蛋白的表达,但这种作用可被Atro逆转。提示胆碱类受体参与配基对肿瘤细胞的促增殖作用。 展开更多
关键词 乙酰胆碱 SK—N—SH mAchR1 增殖 SK-N-SH细胞 细胞增殖活性 拮抗剂 毒蕈碱受体亚型 mol/L 间接免疫荧光技术
下载PDF
Muscarinic acetylcholine receptor M3 in proliferation and perineural invasion of cholangiocarcinoma cells 被引量:4
5
作者 Yu-Jie Feng,Bing-Yuan Zhang,Ru-Yong Yao and Yun LuSecond Department of General Surgery and Central Laboratory of Molecular Biology,Affiliated Medical College Hospital,Qingdao University,Qingdao 266003,China 《Hepatobiliary & Pancreatic Diseases International》 SCIE CAS 2012年第4期418-423,共6页
BACKGROUND:Cholangiocarcinoma,a type of malignant tumor,originates from epithelial cells of the bile duct.Perineural invasion is common path for cholangiocarcinoma metastasis,and it is highly correlated with postopera... BACKGROUND:Cholangiocarcinoma,a type of malignant tumor,originates from epithelial cells of the bile duct.Perineural invasion is common path for cholangiocarcinoma metastasis,and it is highly correlated with postoperative recurrence and poor prognosis.It has been reported that muscarinic acetylcholine receptor M3(mAChR M3) is widely expressed in digestive tract cancer,and may play an important role in the proliferation,differentiation,transformation and carcinogenesis of tumors.This study was to explore the effect of mAChR M3 on the growth of cholangiocarcinoma cells in vitro and provide a new approach to the pathogenesis and treatment of cholangiocarcinoma.METHODS:Streptavidin-biotin complex immunohistochemistry was carried out to assess the expression of mAChR M3 in surgical specimens of cholangiocarcinomas(40 cases) and normal bile duct tissues(9),as well as to investigate nerve infiltration.The cholangiocarcinoma cells were treated with different concentrations of selective M-receptor agonist pilocarpine and M-receptor blocker atropine sulfate to induce changes in cell proliferation.The experimental data were analyzed by the Chi-square test.RESULTS:The strongly-positive expression rate of mAChR M3 was much higher in poorly-differentiated(69%,9/13) than in well-and moderately-differentiated cholangiocarcinomas(30%,8/27)(χ 2 =5.631,P<0.05).The strongly-positive mAChR M3 expression rate in hilar cholangiocarcinoma(50%,14/28) was higher than that in cholangiocarcinomas from the middle and lower common bile duct(25%,3/12)(χ 2 =2.148,P<0.05).Cholangiocarcinomas with distant metastasis had a stronglypositive expression rate(75%,9/12),which was much higher than those without distant metastasis(29%,8/28)(χ 2 =7.410,P<0.01).The absorbance value in the pilocarpine+atropine group was significantly higher than the corresponding value in the pilocarpine group.CONCLUSIONS:The expression of mAChR M3 is influenced by the extent of differentiation,distant metastasis and the site of cholangiocarcinoma.It also plays a key role in the proliferation and metastasis of cholangiocarcinoma. 展开更多
关键词 CHOLANGIOCARCINOMA mAChR M3 IMMUNOHISTOCHEMISTRY perineural invasion PROLIFERATION
下载PDF
Anti-M<sub>3</sub>Muscarinic Acetylcholine Receptor Antibodies in Systemic Lupus Erythematosus
6
作者 Silvia Reina Cecilia Pisoni +3 位作者 Alicia Eimon Carolina Carrizo Roberto Arana Enri Borda 《Pharmacology & Pharmacy》 2015年第1期25-33,共9页
Background: Evidences have shown that anti-M3 muscarinic acetylcholine receptor IgG (anti-M3 mAChR IgG) are clinically useful autoantibody that exert a cholinergic pharmacologic effect binding and interacting with M3 ... Background: Evidences have shown that anti-M3 muscarinic acetylcholine receptor IgG (anti-M3 mAChR IgG) are clinically useful autoantibody that exert a cholinergic pharmacologic effect binding and interacting with M3 mAChR at the level of exocrine gland (salivary and ocular). Aims: The aim of this study was to determine the associations between serum level of anti-M3 mAChR IgG in patients with systemic lupus erythematosus (SLE) and other autoantibodies, serum prostaglandin E2 (PGE2), and clinical manifestations. Methods: Serum autoantibodies against M3 mAChR synthetic peptide were measured by enzyme-linked immuno absorbent assay (ELISA) using, as an antigen, a 25-mer peptide K-R-T-V-P-D-N-Q-C-F-I-Q-F-L-S-N-P-A-V-T-F-G-T-A-I corresponding to the amino acid sequence of the second extracellular loop of the human M3 mAChR. Serum levels of antinuclear antibodies (ANA), anti-Smith (Sm) antibodies, anti-phospholipid (APL) antibodies, and PGE2 were determined by ELISA in patients with SLE. Results: We found significantly enhanced titers of anti-M3 mAChR IgG in sera from SLE patients compared with healthy individuals (control). In addition, serum levels of PGE2 were significantly higher in SLE patients than in control patients and were significantly higher in active than in non-active SLE. No correlation was found with other autoantibodies present in SLE. By contrast, a positive correlation was found between anti-M3 mAChR IgG and PGE2 serum levels in SLE. Conclusions: As anti-M3 mAChR antibodies present in the sera of SLE patients may be another factor in the pathogenesis of this disease, and the increment of PGE2 in the sera of SLE has a modulatory action on the inflammatory process, suggesting that the presence of these autoantibodies against M3 mAChR may contribute to sustained immune deregulation and the strong inflammatory component observed in SLE. 展开更多
关键词 Anti-M3 MACHR ANTIBODIES Systemic Lupus ERYTHEMATOSUS PROSTAGLANDIN E2
下载PDF
Role of M<sub>3</sub>Muscarinic Acethylcholine Receptor Antibodies as a New Marker in Primary Sjögren Syndrome
7
作者 Silvia Reina Cecilia Pisoni +2 位作者 Roberto Arana Sabrina Ganzinelli Enri Borda 《Pharmacology & Pharmacy》 2017年第7期242-252,共11页
Aims: This paper investigates the presence of M3 muscarinic acetylcholine receptor autoantibody present in the serum of patients with primary Sj?gren syndrome (pSS). Main methods: We detected the levels of M3mAChR pep... Aims: This paper investigates the presence of M3 muscarinic acetylcholine receptor autoantibody present in the serum of patients with primary Sj?gren syndrome (pSS). Main methods: We detected the levels of M3mAChR peptide IgG, PGE2, IL-1β in serum of SS patients using the enzyme-linked immune sorbent assay (ELISA). To measure the quantity of nitrite/nitrate, we used Griess reagent system. Key findings: Titres of M3mAChR antibody in sera from SS patients are significantly enhanced compared to healthy subjects (control). The enhancement of these autoantibodies is accompanied by the increase of the levels of PGE2, IL-1β and nitrite/nitrate in serum. Under in vitro conditions, the synthetic human M3 peptide impaires the increment of M3mAChR antibody but not that of nati-Ro/SSA antibody. In positive anti-Ro/SSA antibody patients, the increment of M3mAChR peptide IgG and the measured pro-inflammatory substances is related. Significance: On this basis, anti M3mAChR peptide IgG can be said to act as a modulator of the immune system and to play a role in the host-chronic increment of proinflammatory substances in SS patients with positive Ro/SSA antibody. This association between the antibody and the pathogenesis of SS disease may result in useful predicting SS. 展开更多
关键词 Anti-Ro/SSA Antibody ANTI M3mAChR Peptide IgG IL-1β PGE2 NITRIC Oxide
下载PDF
毒蕈碱样乙酰胆碱受体m1~m5亚基在大鼠前庭终器组织中的表达 被引量:1
8
作者 程华茂 孔维佳 姚琦 《临床耳鼻咽喉科杂志》 CSCD 北大核心 2006年第22期1027-1029,共3页
目的:检测大鼠前庭终器中毒蕈碱样乙酰胆碱受体(mAChRs)m1~m5哑基的表达。方法:根据GeneBank公布的大鼠mAChR m1~m5亚基的mRNA序列设计特异性引物,再运用RTPCR方法检测大鼠前庭终器中编码mAChR m1~m5亚基的mRNA的表达,之后行PC... 目的:检测大鼠前庭终器中毒蕈碱样乙酰胆碱受体(mAChRs)m1~m5哑基的表达。方法:根据GeneBank公布的大鼠mAChR m1~m5亚基的mRNA序列设计特异性引物,再运用RTPCR方法检测大鼠前庭终器中编码mAChR m1~m5亚基的mRNA的表达,之后行PCR产物直接测序。以大鼠脑千组织提取RNA为阳性对照,以解剖液为阴性对照。结果:扩增出标志mAChR m1~m5亚基表达的PCR产物,并经测序证实与预计扩增的cDNA片段序列一致。结论:在大鼠前庭终器组织中有mAChR m1~m5亚基的表达,为乙酰胆碱作为大鼠外周前庭系统冲经递质提供了最直接的证据。 展开更多
关键词 前庭 功能试验 MACHR RT—PCR
原文传递
Localization of muscarinic acetylcholine receptor in plant guard cells 被引量:2
9
作者 Fanxia Meng Xin Liu +1 位作者 Shuqiu Zhang Chenghou Lou 《Chinese Science Bulletin》 SCIE EI CAS 2001年第7期586-588,618,共4页
Acetylcholine (ACh), as an important neuro-transmitter in animals, also plays a significant role in various kinds of physiological functions in plants. But relatively little is known about its receptors in plants. A g... Acetylcholine (ACh), as an important neuro-transmitter in animals, also plays a significant role in various kinds of physiological functions in plants. But relatively little is known about its receptors in plants. A green fluorescence BODIPY FL-labeled ABT, which is a high affinity ligand of muscarinic acetylcholine receptor (mAChR), was used to localize mAChR in plant guard cells. In Vicia faba L. and Pisum sativum L., mAChR was found both on the plasma membrane of guard cells. mAChR may also be distributed on guard cell chloroplast membrane of Vicia faba L. The evidence that mAChR localizes in the guard cells provides a new possible signal transduction pathway in ACh mediated stomata movement. 展开更多
关键词 GUARD cell MACHR FLUORESCENT LOCALIZATION VICIA faba L. PISUM sativum L.
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部