Triggle C R, Grant W F, Triggle D J
J Pharmacol Exp Ther. 1975 Jul;194(1):182-90.
Pretreatment of the guinea-pig ileal longitudinal muscle preparation with cadmium (Cd++) in the concentration range 5 to 1000 muM resulted in an inhibition of the phasic and tonic contractions induced by both high potassium and the muscarinic agonist, cis-2-methyl-4-dimethylaminomethyl-1,3-dioxolane methiodide. The K+ contracture was significantly more sensitive to the inhibitory action of Cd++ in the concentration range 5 to 100 muM, but not at concentrations of Cd++ above 100 muM. Low concentrations of Cd++, 0.1 to 0.01 muM, were found to increase by an atropine-sensitive mechanism, the spontaneous activity of approximately 50% of the preparations tested. It was also shown that the ionophore A23187 produced a concentration-dependent contraction in the guinea-pig ileal longitudinal muscle that was dependent upon the presence of extracellular calcium. When 1.8 mM Cd++ was added to a tissue that had been incubated in Ca++-free media for 60 minutes and pretreated with 5 muM A23187 for 15 minutes, a slow contractile response was recorded. Similar, but significantly smaller, contractions were also recorded when 1.8 mM Ca++, Mn++, Sr++, Pb++ and Ba++, but not when Co++, Ni++, Hg++, UO2++, and Tm++ and Th++++ were administered. It was concluded that the contractile action of these cations was dependent on ionic radius, hydration energy, valency and, perhaps, coordination number, and was due to the intracellular entry of the cation where it resulted in the release of bound Ca++ and/or directly activated the smooth muscle troponin system.
用浓度范围为5至1000μM的镉(Cd++)预处理豚鼠回肠纵肌标本,可抑制高钾和毒蕈碱激动剂顺-2-甲基-4-二甲基氨基甲基-1,3-二氧戊环甲碘化物诱导的相性和强直性收缩。在5至100μM浓度范围内,K+挛缩对Cd++的抑制作用明显更敏感,但在Cd++浓度高于100μM时则不然。发现低浓度的Cd++(0.1至0.01μM)通过阿托品敏感机制增加了约50%受试标本的自发活动。还表明,离子载体A23187在豚鼠回肠纵肌中产生浓度依赖性收缩,该收缩依赖于细胞外钙的存在。当将1.8 mM Cd++添加到在无钙培养基中孵育了60分钟并预先用5μM A23187处理了15分钟的组织中时,记录到缓慢的收缩反应。当给予1.8 mM Ca++、Mn++、Sr++、Pb++和Ba++时也记录到类似但明显较小的收缩,而给予Co++、Ni++、Hg++、UO2++、Tm++和Th++++时则未记录到收缩。得出的结论是,这些阳离子的收缩作用取决于离子半径、水化能、化合价以及可能的配位数,并且是由于阳离子进入细胞内,在那里导致结合的Ca++释放和/或直接激活平滑肌肌钙蛋白系统。