首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Lack of effect of zaprinast on methacholine-induced contraction and inositol 145-trisphosphate accumulation in bovine tracheal smooth muscle.
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Lack of effect of zaprinast on methacholine-induced contraction and inositol 145-trisphosphate accumulation in bovine tracheal smooth muscle.

机译:扎普利斯特对牛气管平滑肌中乙酰甲胆碱引起的收缩和肌醇145-三磷酸积累缺乏影响。

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摘要

1. The effects of zaprinast (M&B 22948), a selective guanosine 3':5'-cyclic monophosphate (cyclic GMP) phosphodiesterase inhibitor, and sodium nitroprusside on cyclic GMP content, phosphoinositide hydrolysis and airway smooth muscle tone were examined in flurbiprofen pretreated bovine tracheal smooth muscle (BTSM). 2. Anion-exchange chromatography of the soluble fraction of BTSM homogenates resolved three peaks of Ca2+/calmodulin-independent phosphodiesterase (PDE) activity that corresponded to type Ia (cyclic GMP-specific, zaprinast-inhibitable), type II (cyclic GMP-stimulated) and type IV (Ro 20 1724-inhibitable) PDE isoenzymes. Zaprinast caused a selective inhibition of the type Ia PDE isoenzyme (IC50 0.94 microM) with respect to the type II and IV (IC50 s 93 microM and 197 microM respectively) isoenzymes. 3. Pretreatment of BTSM strips with zaprinast (10 microM) for 20 min affected neither the initial rate of force development, nor the resultant magnitude of contraction induced by methacholine (10 microM). In addition, zaprinast (10 microM; 20 min) did not affect the cumulative concentration-response relationship induced by methacholine. In contrast, sodium nitroprusside (300 microM) either alone, or in combination with zaprinast (10 microM), significantly attenuated tone induced by low, but not high concentrations of methacholine. This resulted in a non-parallel, rightwards shift of the methacholine concentration-response curves (nitroprusside: 4.0 fold; nitroprusside/zaprinast: 4.8 fold at the EC50 values), without a reduction in the maximum tone generated. 4. In BTSM slices, zaprinast (10 or 100 microM) did not influence basal or methacholine (10 microM)-stimulated cyclic GMP accumulation or inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) mass accumulation over a 60s incubation period, although it did significantly increase cyclic GMP content over longer (30 min) stimulation periods.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在氟比洛芬预处理的牛中检查了zaprinast(M&B 22948),一种选择性的鸟苷3':5'-环一磷酸(环GMP)磷酸二酯酶抑制剂和硝普钠对环GMP含量,磷酸肌醇水解和气道平滑肌张力的影响。气管平滑肌(BTSM)。 2. BTSM匀浆的可溶性级分的阴离子交换色谱法解析了Ca2 + /钙调蛋白非依赖性磷酸二酯酶(PDE)活性的三个峰,分别对应于Ia型(环状GMP特异性,扎巴司特抑制),II型(环状GMP刺激) )和IV型(Ro 20 1724抑制型)PDE同工酶。 Zaprinast相对于II型和IV型(IC50分别为93 microM和197 microM)同功酶对Ia PDE型同功酶(IC50为0.94 microM)产生选择性抑制。 3.用扎必利斯特(10 microM)预处理BTSM条带20分钟既不影响最初的力量发展速度,也不影响由乙酰甲胆碱(10 microM)引起的最终收缩幅度。此外,扎必利斯特(10 microM; 20分钟)不影响乙酰甲胆碱诱导的累积浓度-反应关系。相比之下,硝普钠(300 microM)单独使用或与扎普力纳(10 microM)联合使用,可显着减弱由低浓度但非高浓度的甲胆碱引起的音调。这导致乙酰甲胆碱浓度-响应曲线发生非平行,向右的移动(在EC50值下硝普钠:4.0倍;硝普钠/扎普那司:4.8倍),而不会降低最大产生的色调。 4.在BTSM切片中,扎普利斯特(10或100 microM)不会影响基础或乙酰甲胆碱(10 microM)刺激的循环GMP积累或肌醇1,4,5-三磷酸(Ins(1,4,5)P3)的质量积累在60 s的潜伏期中,尽管它在更长(30分钟)的刺激时间内确实显着增加了循环GMP含量。(摘要截断为250字)

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