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11.
Parimal C. Sen Zhou Meng Ai Tushar K. Ray 《Archives of biochemistry and biophysics》1980,205(2):340-351
The transversal distribution of the free NH2 groups associated with phosphatidyl ethanolamine and the intrinsic membrane proteins of the purified pig gastric microsomes was quantitated and their relations to the function of the gastric K+-stimulated ATPase was investigated. Three different chemical probes such as 2,4,6-trinitrobenzene sulfonic acid (TNBS), 1-fluoro-2,4-dinitrobenzene (FDNB), and 2-methoxy-2,4-diphenyl-3(2H)-furanone (MDPF) were used for the study. The structure-function relationship of the membrane NH2 groups was studied after modification with the probes under various conditions and relating the inhibition of the K+-stimulated ATPase to the ATPase-dependent H+ accumulation by the gastric microsomal vesicles. TNBS (2 mm) inhibits nearly completely the K+-stimulated ATPase and the vesicular dye accumulation, both in presence and absence of valinomycin plus K+. Both the K+-ATPase and dye uptake were largely (about 50%) protected against TNBS inhibition if the treatment with TNBS was carried out in presence of 2 mm ATP. TNBS and FDNB labeled 70% of the total microsomal PE; the intra- and extravesicular orientation being 48 and 22%, respectively. The presence or absence of ATP did not have any effect on the TNBS labeling of microsomal PE. ATP, however, significantly (P < 0.05) reduced the labeling of protein-bound NH2 groups of gastric microsomes by TNBS. The intra- and extravesicular orientation of the protein NH2 groups were 60 and 40%, respectively. Eighteen percent of the total protein-NH2 appeared to be associated with the K+-stimulated ATPase; the rest being associated with non-ATPase proteins of the microsomes. About half (50%) of the total free NH2 groups of the K+-stimulated ATPase were exposed to the vesicle exterior and were found to play critical roles in gastric ATPase function. The generation of florescence after MDPF conjugation of gastric microsomes was largely (50%) inhibited by ATP. ATP also protected completely the MDPF inhibition of gastric K+-stimulated ATPase and dye uptake. 相似文献
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Kalthoum Tizaoui Jae Won Yang Keum Hwa Lee Ji Hong Kim Minseok Kim Sojung Yoon Yeonwoo Jung Joon Beom Park Kitae An Hyeok Choi Donggyu Song HyunTaek Jung Seongmin Ahn Taeho Yuh Hee Min Choi Jae Ha Ahn Younjuong Kim Sanghyun Jee Hyeongsun Lee Soohwa Jin Jun-Gu Kang Bohyun Koo Joo Yeop Lee Kyoung Min Min Wonseok Yoo Hyeong Jun Rhyu Yeonjung Yoon Min Ho Lee Sung Eun Kim Jimin Hwang Ai Koyanagi Louis Jacob Seoyeon Park Jae Il Shin Lee Smith 《International journal of biological sciences》2022,18(9):3731
YKL-40, a chitinase-3-like protein 1 (CHI3L1) or human cartilage glycoprotein 39 (HC gp-39), is expressed and secreted by various cell-types including macrophages, chondrocytes, fibroblast-like synovial cells and vascular smooth muscle cells. Its biological function is not well elucidated, but it is speculated to have some connection with inflammatory reactions and autoimmune diseases. Although having important biological roles in autoimmunity, there were only attempts to elucidate relationships of YKL-40 with a single or couple of diseases in the literature. Therefore, in order to analyze the relationship between YKL-40 and the overall diseases, we reviewed 51 articles that discussed the association of YKL-40 with rheumatoid arthritis, psoriasis, systemic lupus erythematosus, Behçet disease and inflammatory bowel disease. Several studies showed that YKL-40 could be assumed as a marker for disease diagnosis, prognosis, disease activity and severity. It is also shown to be involved in response to disease treatment. However, other studies showed controversial results particularly in the case of Behçet disease activity. Therefore, further studies are needed to elucidate the exact role of YKL-40 in autoimmunity and to investigate its potential in therapeutics. 相似文献
14.
本文在培养的大鼠三叉神经节(trigeminal ganglion,TG)神经元上采用全细胞膜片钳技术,探讨大麻素对大鼠TG神经元ATP激活电流(ATP-activated currents,IATP)的影响.结果显示(1)胞外给予ATP,大部分受检细胞(67/75,89.33%)可记录到一个内向电流,且具有剂量依赖性.该电流可被P2X嘌呤受体特异性拮抗剂PPADS所阻断.(2)预加WIN55212-2[大麻素受体1(cannabinoid receptor 1,CB1受体)激动剂]可对IATP产生抑制作用,此作用呈剂量依赖性,并可被CB1受体特异性拮抗剂AM281阻断.预加不同浓度的WIN55212-2(1x10-13、1x10-12、1x10-11、1x10-10、1x10-9和1x10-8mol/L)对IATP(1x10-4mol/L ATP)的抑制作用分别为(8.14±3.14)%、(20.11±2.72)%、(46.62±3.51)%、(72.16±5.64)%、(80.21±2.80)%和(80.59±3.55)%.(3)预加WIN55212-2后IATP的浓度-反应曲线明显下移;最大反应浓度时的IATP幅值减小了(58.02±4.21)%,而阈值基本不变;预加WIN55212.2前后曲线的EC50值非常接近(1.15x10-4mol/L vs 1.27x10-4 mol/L).(4)预加forskolin[腺苷酸环化酶(adenylyl cyclase,AC)激动剂]或8-Br-cAMP可以逆转WIN55212-2对IATP的抑制作用.以上结果表明,大麻素可能作用于CB1受体,通过抑制AC-cAMP-PKA途径发挥对IATP的抑制作用. 相似文献
15.
同型半胱氨酸对大鼠血管平滑肌细胞增殖的作用 总被引:11,自引:0,他引:11
血中同型半胱氨酸(homocysteine,HCY)浓度的升高已成为动脉粥样硬化发生的一个独立危险因子.为进一步阐明HCY促进血管平滑肌细胞(vascularsmoothmusclecels,VSMCs)增殖,从而引起动脉粥样硬化发生的机理.本实验采用细胞计数、3H-TdR参入、细胞周期分析、Northern杂交方法证明,一定剂量的HCY可促进离体培养的WKY大鼠血管平滑肌细胞增殖,使其DNA合成增加,细胞周期中S期细胞所占比例增加43%,并促进c-myc与c-fos原癌基因mRNA表达增加.提示HCY可能通过促进VSMCs增殖而诱发动脉粥样硬化 相似文献
16.
流行性出血热地鼠肾细胞灭活疫苗人体试用细胞免疫反应观察 总被引:2,自引:0,他引:2
观察了20位志愿者在接种试验性流行性出血热(EHF)地鼠肾细胞(GHKC)双价灭活疫苗后的细胞免疫反应,并以其体液免疫反应作对照观察。用淋巴细胞转化试验测定细胞免疫水平。结果首针疫苗接种后42天和56天,特异性刺激指数(SSI)和非特异性刺激指数(NSI)均较免疫前显著增高(P_(SSI)<0.001;P_(NSI)<0.02),免疫后SSI累计阳转率为100%,NSI累计阳转率为60%,免疫后6个月二者均降低至正常水平。免疫后56天测定抗体,荧光抗体阳转率为100%;微量感染性中和试验表明,针对家鼠型病毒L99株中和抗体阳转率为95%,而针对野鼠型病毒JR株阳转率为65%。 相似文献
18.
窝雏数处理对两种雀形目幼鸟生长的影响 总被引:6,自引:0,他引:6
基于 1 997~ 1 999年野外实验 ,对高寒草甸小云雀和黄嘴朱顶雀两种雀形目鸟的窝雏数进行增减处理。结果表明 ,对照组的幼鸟生长率和离巢体重都大于增加组 ,说明窝雏数增加后 ,幼鸟质量下降。随着窝雏数增加 ,这两种幼鸟生长率显著下降 (小云雀 :r =-0 965 ,P =0 0 3 5 <0 0 5 ;朱顶雀 :r =-0 82 8,P =0 0 2 2 <0 0 5 )。窝雏数改变对小云雀幼鸟出飞重影响不显著 (r =-0 41 8,P =0 5 2 8>0 0 5 ) ,而对黄嘴朱顶雀有显著的影响 (r=-0 90 1 ,P =0 0 1 4<0 0 5 )。 相似文献
19.
目的:观察肺纤维化初期肺动脉高压大鼠肺动脉血管反应性的变化。方法:66只雄性SD大鼠,随机分为博莱霉素(BLM)组和手术对照(Sham)组。BLM组为气管内一次性滴注BLM(5 mg/kg);Sham组为气管内滴注等容量的生理盐水(NS)。应用离体血管张力检测技术测定大鼠肺动脉血管反应性变化;用HE显示肺动脉壁病理形态学变化;Masson染色检测肺纤维化程度;右心漂浮导管技术测定大鼠平均肺动脉压。结果:①BLM组大鼠的肺动脉血管(保留内皮和去内皮)对苯肾上腺素(PE)的收缩反应均弱于Sham组(P均〈0.05)。②BLM组大鼠肺动脉血管(保留内皮)对氯化乙酰胆碱(Ach)的舒张反应明显弱于Sham组(P〈0.01)。③Sham组有内皮的肺动脉血管对L-NAME和PE联合作用的收缩反应明显强于PE单独作用(P〈0.01),而BLM组有内皮肺动脉血管对L-NAME和PE联合作用的收缩反应与对PE单独作用比,其差异无统计学意义(P〉0.05)。④BLM组肺动脉内皮细胞脱落。⑤BLM组大鼠肺组织呈现纤维增生初期的病理特征,且大鼠的平均肺动脉压明显高于Sham组(P〈0.05)。结论:肺纤维化形成初期肺动脉高压大鼠肺动脉血管反应性出现异常。 相似文献
20.
Inhibition of mitochondrial complex I improves glucose metabolism independently of AMPK activation
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Wo‐Lin Hou Jun Yin Miriayi Alimujiang Xue‐Ying Yu Li‐Gen Ai Yu‐qian Bao Fang Liu Wei‐Ping Jia 《Journal of cellular and molecular medicine》2018,22(2):1316-1328
Accumulating evidences showed metformin and berberine, well‐known glucose‐lowering agents, were able to inhibit mitochondrial electron transport chain at complex I. In this study, we aimed to explore the antihyperglycaemic effect of complex I inhibition. Rotenone, amobarbital and gene silence of NDUFA13 were used to inhibit complex I. Intraperitoneal glucose tolerance test and insulin tolerance test were performed in db/db mice. Lactate release and glucose consumption were measured to investigate glucose metabolism in HepG2 hepatocytes and C2C12 myotubes. Glucose output was measured in primary hepatocytes. Compound C and adenoviruses expressing dominant negative AMP‐activated protein kinase (AMPK) α1/2 were exploited to inactivate AMPK pathway. Cellular NAD+/NADH ratio was assayed to evaluate energy transforming and redox state. Rotenone ameliorated hyperglycaemia and insulin resistance in db/db mice. It induced glucose consumption and glycolysis and reduced hepatic glucose output. Rotenone also activated AMPK. Furthermore, it remained effective with AMPK inactivation. The enhanced glycolysis and repressed gluconeogenesis correlated with a reduction in cellular NAD+/NADH ratio, which resulted from complex I suppression. Amobarbital, another representative complex I inhibitor, stimulated glucose consumption and decreased hepatic glucose output in vitro, too. Similar changes were observed while expression of NDUFA13, a subunit of complex I, was knocked down with gene silencing. These findings reveal mitochondrial complex I emerges as a key drug target for diabetes treatment. Inhibition of complex I improves glucose homoeostasis via non‐AMPK pathway, which may relate to the suppression of the cellular NAD+/NADH ratio. 相似文献