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四磺酸酞菁铝(A1PcS4)对平滑肌的光动力作用:硫醇和环鸟苷酸类似物的影响。

Photodynamic action of aluminium phthalocyanine tetrasulphonate (A1PcS4) on smooth muscle: effects of thiols and a cyclic GMP analogue.

作者信息

Matthews E K, Flaherty C, Smith W H

机构信息

Department of Pharmacology, University of Cambridge.

出版信息

Br J Pharmacol. 1993 Nov;110(3):1248-54. doi: 10.1111/j.1476-5381.1993.tb13949.x.

Abstract
  1. The smooth muscle system of the guinea-pig taenia caeci has been used in vitro to characterize the photodynamic action of aluminium phthalocyanine tetrasulphonate (A1PcS4) in the presence or absence of the thiol reductants L-cysteine (Cys), N-acetyl-L-cysteine (NAC), DL-dithiothreitol (DTT) or reduced glutathione (GSH). 2. In all photodynamic experiments the muscle was exposed to A1PcS4 (10(-5) M) for 30 min, followed by a 30 min washout period before photon irradiation at 32,000 lux (lambda > 570 nm) for 30 min. Photodynamic contractions were measured relative to the contractile response to carbachol (5 x 10(-5) M) and relaxation responses were determined in muscle precontracted with either carbachol 5 x 10(-5) M or KCl 23.5 mM. 3. Photon-activation of A1PcS4-sensitized smooth muscle evoked a triphasic response: an initial transient contraction and subsequent relaxation followed by a secondary sustained contraction. Cys 10 mM, NAC 10 mM and DTT 5 mM had no effect on the initial photodynamic contraction but significantly decreased the magnitude of the sustained contraction from mean values of 98% to 18%, 95% to 72% and 93% to 6% of the standard carbachol contraction (5 x 10(-5) M), respectively; GSH 10 mM was without significant effect on either the initial or sustained contraction. 4. In the absence of extracellular calcium the A1PcS4-sensitized smooth muscle did not respond to photon activation but re-introduction of calcium after cessation of illumination produced a sustained contraction which was markedly inhibited by Cys 10 mM. 5. In precontracted AlPcS4-treated muscle preparations photon activation produced a triphasic relaxation response, i.e. a rapid relaxation followed by a transient contraction and a secondary more sustained relaxation. The sustained phase of photodynamic relaxation was potentiated significantly by Cys 10 mM,NAC 10 mM, DTT 5 mM and GSH 10 mM, the relaxation being approximately doubled in magnitude from mean values of 34% to 68%, 30% to 73%, 34% to 68%, and 48% to 77%, respectively, relative to the standard carbachol (5 x l0-5 M) response.6. The cyclic GMP analogue, 8-(4-chlorophenylthio)-guanosine-3':5'-cyclic monophosphate (8-PCPTcGMP)(2 x 10-4 M) alone caused a triphasic relaxation response similar to that produced by photon activation of an AIPcS4-sensitized precontracted preparation in the presence of thiol reductants. The pattern of 8-PCPT-cGMP-induced relaxation was similar in muscle precontracted with carbachol 5 x 10-5M or KCI 23.5 mM.7. It is concluded that the rapid generation of reactive intermediates by photon-activation of boundAlPcS4 leads to membrane permeabilization, calcium entry and muscle contraction. These effects may be opposed by a direct stimulatory action of singlet oxygen on guanylate cyclase which is enhanced by the action of thiol reagents and mimicked by the cyclic GMP analogue, 8-PCPT-cGMP.
摘要
  1. 豚鼠盲肠带的平滑肌系统已被用于体外实验,以表征在存在或不存在硫醇还原剂L-半胱氨酸(Cys)、N-乙酰-L-半胱氨酸(NAC)、二硫苏糖醇(DTT)或还原型谷胱甘肽(GSH)的情况下,四磺基铝酞菁(A1PcS4)的光动力作用。2. 在所有光动力实验中,肌肉先暴露于A1PcS4(10⁻⁵ M)30分钟,随后经过30分钟的洗脱期,然后在32000勒克斯(λ>570 nm)的光照下照射30分钟。相对于对卡巴胆碱(5×10⁻⁵ M)的收缩反应测量光动力收缩,并在预先用5×10⁻⁵ M卡巴胆碱或23.5 mM氯化钾预收缩的肌肉中测定松弛反应。3. A1PcS4致敏的平滑肌的光子激活引发了三相反应:最初的短暂收缩,随后是松弛,接着是二次持续收缩。10 mM的Cys、10 mM的NAC和5 mM的DTT对最初的光动力收缩没有影响,但显著降低了持续收缩的幅度,相对于标准卡巴胆碱收缩(5×10⁻⁵ M)的平均值,分别从98%降至18%、95%降至72%和93%降至6%;10 mM的GSH对最初或持续收缩均无显著影响。4. 在没有细胞外钙的情况下,A1PcS4致敏的平滑肌对光子激活无反应,但在光照停止后重新引入钙会产生持续收缩,该收缩被10 mM的Cys显著抑制。5. 在预先收缩的经A1PcS4处理的肌肉制剂中,光子激活产生了三相松弛反应,即快速松弛,随后是短暂收缩和二次更持续的松弛。10 mM的Cys、10 mM的NAC、5 mM的DTT和10 mM的GSH显著增强了光动力松弛的持续阶段,相对于标准卡巴胆碱(5×10⁻⁵ M)反应,松弛幅度分别从平均值的34%增加到68%、30%增加到73%、34%增加到68%和48%增加到77%。6. 环鸟苷酸类似物8-(4-氯苯硫基)-鸟苷-3':5'-环一磷酸(8-PCPTcGMP)(2×10⁻⁴ M)单独引起的三相松弛反应类似于在存在硫醇还原剂的情况下,AIPcS4致敏的预先收缩制剂的光子激活所产生的反应。在预先用5×10⁻⁵ M卡巴胆碱或23.5 mM氯化钾预收缩的肌肉中,8-PCPT-cGMP诱导的松弛模式相似。7. 得出的结论是,结合的A1PcS4的光子激活快速产生活性中间体导致膜通透性增加、钙内流和肌肉收缩。这些作用可能被单线态氧对鸟苷酸环化酶的直接刺激作用所抵消,这种刺激作用通过硫醇试剂的作用增强,并被环鸟苷酸类似物8-PCPT-cGMP模拟。

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