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血小板活化因子对豚鼠离体心房收缩力和45Ca通量的影响。

Effects of platelet activating factor on contractile force and 45Ca fluxes in guinea-pig isolated atria.

作者信息

Diez J, Delpón E, Tamargo J

机构信息

Instituto de Farmacología y Toxicología, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

Br J Pharmacol. 1990 Jun;100(2):305-11. doi: 10.1111/j.1476-5381.1990.tb15800.x.

Abstract
  1. The effects of platelet activating factor (PAF) were studied on the electromechanical properties and 45Ca2+ fluxes of guinea-pig isolated atria. 2 Both in spontaneously beating and electrically driven atria, PAF (10(-12)-10(-7) M) increased atrial rate but produced a biphasic effect on contractile force. At low concentrations (up to 10(-10) M) it produced a positive inotropic effect, while at higher concentrations PAF exerted a negative inotropic effect. A similar biphasic effect was observed in the slow contractions elicited by isoprenaline in K(+)-depolarized atrial fibres. 3. The positive inotropic effect of PAF was prevented by verapamil, whereas pretreatment of atria with propranolol, phentolamine, indomethacin or atropine did not modify its positive and negative inotropic actions. BN 52021, a specific PAF antagonist, abolished both the positive and negative inotropic effects. 4. PAF had no effect on the characteristics of the action potentials recorded in either normally polarized or K(+)-depolarized (slow action potential) atrial fibres. 5. At concentrations at which it increased contractile force, PAF potentiated the contractile responses to Ca2+ (0.9-9 mM), whereas at negative inotropic concentrations it inhibited them. The negative inotropic effect of PAF was partially reversed in 70% Na+ medium. 6. At 10(-11) M, PAF increased 45Ca2+ uptake and reduced the rate coefficient (kcm) for the 45Ca2+ efflux. This increase in 45Ca2+ uptake was abolished in atria pretreated with verapamil or BN 52021. However, 10(-7) M PAF modified neither 45Ca2+ uptake nor efflux in atrial muscle. 7. These results suggest that in guinea-pig atria the biphasic inotropic effects of PAF cannot be explained through modifications in the slow inward Ca2+ current or in Na'-Ca2+ exchange, but may be related to changes in trans-sarcolemmal Ca2 + entry mediated by specific PAF receptors.
摘要
  1. 研究了血小板活化因子(PAF)对豚鼠离体心房机电特性和45Ca2+通量的影响。2. 在自发搏动和电驱动的心房中,PAF(10^(-12)-10^(-7) M)均能增加心房率,但对收缩力产生双相作用。在低浓度(高达10^(-10) M)时,它产生正性肌力作用,而在高浓度时PAF发挥负性肌力作用。在K(+)去极化心房纤维中由异丙肾上腺素引发的缓慢收缩中也观察到类似的双相作用。3. 维拉帕米可阻止PAF的正性肌力作用,而用普萘洛尔、酚妥拉明、吲哚美辛或阿托品预处理心房并未改变其正性和负性肌力作用。特异性PAF拮抗剂BN 52021消除了正性和负性肌力作用。4. PAF对正常极化或K(+)去极化(慢动作电位)心房纤维中记录的动作电位特征无影响。5. 在增加收缩力的浓度下,PAF增强了对Ca2+(0.9-9 mM)的收缩反应,而在负性肌力浓度时则抑制它们。PAF的负性肌力作用在70% Na+培养基中部分逆转。6. 在10^(-11) M时,PAF增加45Ca2+摄取并降低45Ca2+外流的速率系数(kcm)。在用维拉帕米或BN 52021预处理的心房中,这种45Ca2+摄取的增加被消除。然而,10^(-7) M PAF对心房肌中的45Ca2+摄取和外流均无影响。7. 这些结果表明,在豚鼠心房中,PAF的双相肌力作用不能通过慢内向Ca2+电流或Na+-Ca2+交换的改变来解释,而可能与由特异性PAF受体介导的跨肌膜Ca2+内流变化有关。

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