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首页> 外文期刊>Autonomic neuroscience: basic & clinical >Effects of cooling and ARL 67156 on synaptic ecto-ATPase activity in guinea pig and mouse vas deferens.
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Effects of cooling and ARL 67156 on synaptic ecto-ATPase activity in guinea pig and mouse vas deferens.

机译:冷却和ARL 67156对豚鼠和小鼠输精管突触胞外ATPase活性的影响。

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We have studied the influence of temperature and ARL 67156 on ATP hydrolysis in mouse and guinea pig vas deferens in order to explore the properties of the enzymatic inactivation mechanism proposed to regulate purinergic neurotransmission at the sympathetic neuromuscular junction of smooth muscle. The ectonucleotidase activity was determined by using the malachite green method to measure the inorganic phosphate (Pi) liberated with ATP used as a substrate. ATP hydrolysis in both species was found to be insensitive to ouabain (100 渭M), sodium azide (1 mM), sodium vanadate (100 渭M) and beta-glycerophosphate (10 mM) and was also found to depend on Ca(2+) and Mg(2+). V(MAX) of the ectonucleotidase activity for guinea pig and mouse vas deferens was 958.4+/-66.3 and 79.7+/-8.5 pmol/min/mg, while K(M) was 625.1+/-45.2 and 406.0+/-29.0 渭M, respectively. Cooling the tissues from 35 to 25 degrees C reduced the enzyme activity significantly (P<0.01) by 52.7+/-9.2% in guinea pig vas deferens and 34.9+/-5.3% in mouse vas deferens. ARL 67156 (100 渭M), the specific ecto-ATPase inhibitor, caused a reduction in enzyme activity in guinea pig and mouse vas of 54.1+/-16.4% and 53.0+/-7.6%, respectively (P<0.01). The degree of inhibition of ATP hydrolysis by lowered temperature and 100 渭M ARL 67156 correlates well with the reported potentiation and prolongation of junction potentials under these conditions. It is concluded that ecto-ATPase or a closely related ectonucleotidase plays an important role in the physiological regulation of purinergic neurotransmission.
机译:我们研究了温度和ARL 67156对小鼠和豚鼠输精管ATP水解的影响,以探讨酶促失活机制的性质,该机制旨在调节平滑肌交感神经肌肉交界处的嘌呤能神经传递。通过使用孔雀绿方法测定以ATP为底物释放的无机磷酸盐(Pi)来测定胞外核苷酸酶活性。发现这两种物种中的ATP水解均对哇巴因(100μM),叠氮化钠(1 mM),钒酸钠(100μM)和β-甘油磷酸酯(10 mM)不敏感,并且还依赖于Ca(2 +)和Mg(2+)。豚鼠和输精管的外切核苷酸酶活性的V(MAX)为958.4 +/- 66.3和79.7 +/- 8.5 pmol / min / mg,而K(M)为625.1 +/- 45.2和406.0 +/- 29.0分别为μM。将组织从35摄氏度冷却到25摄氏度,豚鼠输精管的酶活性显着降低(P <0.01)52.7 +/- 9.2%,小鼠输精管的酶活性降低34.9 +/- 5.3%。特异性胞外ATPase抑制剂ARL 67156(100μM)导致豚鼠和小鼠血管中的酶活性分别降低了54.1 +/- 16.4%和53.0 +/- 7.6%(P <0.01)。降低的温度和100μMARL 67156对ATP水解的抑制程度与所报道的在这些条件下的连接电位增强和延长密切相关。结论是胞外ATP酶或密切相关的胞外核苷酸酶在嘌呤能神经传递的生理调节中起重要作用。

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