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排序方式: 共有8175条查询结果,搜索用时 359 毫秒
51.
Ulf Malmqvist Anders Arner Bengt Uvelius 《Pflügers Archiv : European journal of physiology》1991,419(3-4):230-234
The lactate dehydrogenase (LDH) activity and isoform distribution of LDH were investigated in tissue samples from the rat portal vein, aorta and urinary bladder. In addition, samples were obtained from hypertrophic urinary bladder. The total LDH activity per unit smooth muscle volume was higher in the urinary bladder compared to that in portal vein and aorta. Five LDH isoforms, reflecting different combinations of the two polypeptide chains denoted H and M, could be separated by agarose gel electrophoresis. The aorta contained more of the H form compared to the portal vein and urinary bladder. This difference suggests that the aorta, which is a slow smooth muscle, is more adapted for aerobic metabolism than the faster muscles of portal vein and urinary bladder. In the hypertrophic urinary bladder a shift in LDH isoform pattern towards less of the H form was found, which correlates with a better maintenance of contraction in anoxia in this type of hypertrophic smooth muscle. 相似文献
52.
在调查云南少数民族G6PD缺乏症时,采用G6PD硝基四氮唑蓝纸片法筛查,按WHO标准化方法进行生化变异型鉴定,再用错配碱基PCR引入酶切位点法进行DNA突变型研究,首次在傣族中发现G6PDcDNA突变型:1388G→A。 相似文献
53.
54.
萝摩甙抗自由基损伤作用的实验研究 总被引:1,自引:1,他引:1
目的:探讨萝摩甙对自由基所致脑损伤的神经元保护作用及机制。方法:复制脑缺血模型及H2O2诱导神经元损伤模型,分别测定大鼠脑组织、培养神经元中的丙二醛(MDA)含量以及培养神经元中的乳酸脱氢酶(LDH)漏出率、DNA断裂率和羟自由基清除率,观察萝摩甙对损伤神经元的保护作用。结果:萝摩甙可明显降低脑缺血造成的MDA的升高,亦可明显降低H2O2对神经元造成的LDH漏出率、DNA断裂率增加和丙二醛含量的升高,而且随着萝摩甙浓度的升高羟自由基清除率明显升高。结论:萝摩甙可通过清除自由基来保护神经元。 相似文献
55.
We previously demonstrated susceptibility of Leishmania sp. to glibenclamide, a K+-ATP transport blocker which interacts with members of the superfamily of adenosine 5′ triphosphate-binding cassette transporters.
In order to characterize the molecular differences between a sensitive Leishmania strain, NR(Gs), and an experimentally selected glibenclamide-resistant strain, NR(Gr), specific biochemical and functional
parameters have been evaluated both in the wild type and in the resistant strain. Most noteworthy, NR(Gr) exhibit an increased
expression of P-glycoprotein and a decreased activity of functional key enzymes such as acid phosphatase, a prominent virulent
factor of the parasite, and pyruvate kinase, a key control enzyme for both carbohydrate and protein metabolism. The specific
biochemical, metabolic and functional changes observed in the resistant strain correlated with a reduced infectivity of stationary
phase NR(Gr) in J774 macrophages and suggested a mechanism to overcome the effect of glibenclamide.
Received: 21 January 2000 / Accepted: 1 March 2000 相似文献
56.
Isolation and RNA-binding analysis of NAD+-isocitrate dehydrogenases from Kluyveromyces lactis and Schizosaccharomyces pombe 总被引:1,自引:0,他引:1
Krebs cycle NAD+-isocitrate dehydrogenase (Idh) binds to the 5-UTRs of all mitochondrial mRNAs in Saccharomyces cerevisiae. We hypothesize that this leader-binding activity plays a role in translational regulation, thereby linking mitochondrial
biogenesis to the need for respiratory function. Analysis of effects of leader binding on mitochondrial translation is complicated
by the involvement of the enzyme in mitochondrial metabolism. We have therefore searched for an Idh altered in RNA binding,
but retaining full enzyme activity. Idh from Kluyveromyces lactis and Schizosaccharomyces pombe was partially purified and examined for the ability to bind Cox2 mRNA. Sch. pombe Idh, like the S. cerevisiae enzyme, has high affinity for both its own, K. lactis and S. cerevisiaeCOX2 leaders. In contrast, Idh purified from K. lactis shows only low affinity for all mRNAs tested. To determine what distinguishes K. lactis Idh from S. cerevisiae Idh, genes encoding the two subunits of Idh in K. lactis were cloned and sequenced. Sequence comparison revealed high levels of similarity throughout the proteins, in particular
in regions involved in enzyme activity, co-factor and regulator binding. Non-conserved residues between the subunits from
the two yeasts are candidates for involvement in the interaction with RNA.
Received: 19 January 2000 / 24 March 2000 相似文献
57.
N. Zurgil R. Bakimer M. Kaplan P. Youinou Y. Shoenfeld 《Journal of clinical immunology》1991,11(5):239-245
Antimitochondrial antibodies (AMA) may be detected in 95% of patients with primary biliary cirrhosis (PBC). The target autoantigens for the AMA were recently identified as four closely related metabolic enzymes located in the mitochondria. We have purified the pyruvate dehydrogenase (PDH) enzyme from bovine heart, showing that all PBC sera reacted with a 74-kd band. PDH was utilized to establish an ELISA assay for detecting the relevant antibodies. One hundred twelve of 120 sera from patients with PBC (95%) reacted with the PDH but none of the 201 control sera, including normal subjects and a panel of sera from other patients with liver diseases, showed similar reactivity. In 77% of the PBC sera the anti-PDH antibody isotype was identified as a combination of IgG and IgM, while in 18% only IgM was detected. In 5% of the sera the isotype was confined to IgG. PBC sera specifically inhibited the PDH enzyme activity. The enzyme inhibition correlated with the anti-PDH antibody titers. Thus, PDH seems to be one of the major target epitopes for AMA observed in sera of patients with PBC. 相似文献
58.
L. B. Kim 《Bulletin of experimental biology and medicine》2008,146(6):680-681
We studied enzyme systems (lactate dehydrogenase) of mitochondria in cerebral nerve cells in experimental encephalopathy developing
after thermal injury. In animals receiving neuromedin at the early terms after injury, the ratio of forward to reverse lactate
dehydrogenase reactions significantly increased over the first day after injury and returned to normal on day 7.
__________
Translated from Byulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 145, No. 6, pp. 626–627, June, 2008 相似文献
59.
60.
Carlo Capelli Guglielmo Antonutto Paola Zamparo Massimo Girardis Pietro Enrico di Prampero 《European journal of applied physiology》1993,66(3):189-195
Summary The mechanical power (Wtot, W·kg–1) developed during ten revolutions of all-out periods of cycle ergometer exercise (4–9 s) was measured every 5–6 min in six subjects from rest or from a baseline of constant aerobic exercise [50%–80% of maximal oxygen uptake (VO2max)] of 20–40 min duration. The oxygen uptake [VO2 (W·kg–1, 1 ml O2 = 20.9 J)] and venous blood lactate concentration ([la]b, mM) were also measured every 15 s and 2 min, respectively. During the first all-out period, Wtot decreased linearly with the intensity of the priming exercise (Wtot = 11.9–0.25·VO2). After the first all-out period (i greater than 5–6 min), and if the exercise intensity was less than 60% VO2max, Wtot, VO2 and [la]b remained constant until the end of the exercise. For exercise intensities greater than 60% VO2max, VO2 and [la]b showed continuous upward drifts and Wtot continued decreasing. Under these conditions, the rate of decrease of Wtot was linearly related to the rate of increase of V [(d Wtot/dt) (W·kg–1·s–1) = 5.0·10–5 –0.20·(d VO2/dt) (W·kg–1·s–1)] and this was linearly related to the rate of increase of [la]b [(d VO2/dt) (W·kg–1·s–1) = 2.310–4 + 5.910–5·(d [la]b/dt) (mM·s–1)]. These findings would suggest that the decrease of Wtot during the first all-out period was due to the decay of phosphocreatine concentration in the exercising muscles occurring at the onset of exercise and the slow drifts of VO2 (upwards) and of Wtot (downwards) during intense exercise at constant Wtot could be attributed to the continuous accumulation of lactate in the blood (and in the working muscles). 相似文献