Penna Claudia, Pagliaro Pasquale, Rastaldo Raffaella, Di Pancrazio Francesca, Lippe Giovanna, Gattullo Donatella, Mancardi Daniele, Samaja Michele, Losano Gianni, Mavelli Irene
Sezione di Fisiologia, Dipartimento di Neuroscienze and Dipartimento di Scienze Cliniche e Biologiche, Università di Torino, 10100 Turin, Italy.
Am J Physiol Heart Circ Physiol. 2004 Nov;287(5):H2192-200. doi: 10.1152/ajpheart.00327.2004. Epub 2004 Jun 24.
The amplitude of coronary reactive hyperemia (CRH), elicited by 15 s of ischemia, is reduced in hearts subjected to 5 min of ischemic preconditioning (IP). F0F1 ATP synthase activity and ATP concentration are also altered by IP. We hypothesized that F0F1 ATP synthase is differently modulated by the inhibitor protein IF(1) during CRH elicited before (CRHnp) and after (CRHprec) IP. Hemodynamic parameters were recorded in 10 anesthetized goats. Myocardial biopsies were obtained before IP (Cnp), during CRHnp, 4 and 6 min after the onset of CRHnp, after IP (Cprec), during CRHprec, and 4 min after CRHprec. F0F1 ATP synthase activity, ATP concentration, and ATP-to-ADP ratio (ATP/ADP) were determined. Compared with CRHnp, IP blunted CRHprec. F0F1 ATP synthase activity transiently increased during CRHnp, decreased 4 min after CRHnp, and returned to control 2 min later; it was lower after IP (Cprec) and did not change during and after CRHprec. All these changes in activity were modulated by IF1. During CRHnp, ATP concentration and ATP/ADP were reduced compared with Cnp and began to rise 6 min thereafter. During Cprec, both parameters were transiently reduced but increased during and after CRHprec. Hence, during CRHnp, F0F1 ATP synthase activity transiently increases and then decreases significantly. The short-lasting inhibition of the enzyme may explain why a few seconds of occlusion do not induce IP. After IP, F0F1 ATP synthase activity is blunted, and it is not affected by a subsequent 15 s of occlusion, which induces a blunted CRHprec. These results suggest that postischemic long-lasting inhibition of F0F1 ATP synthase activity may be a feature of the preconditioned heart. The increase in ATP concentration after preconditioning is in agreement with previous reports of reduced ATP hydrolysis by cytoplasmic ATPases.
由15秒缺血引发的冠状动脉反应性充血(CRH)的幅度,在经历5分钟缺血预处理(IP)的心脏中降低。F0F1 ATP合酶活性和ATP浓度也因IP而改变。我们假设,在IP之前(CRHnp)和之后(CRHprec)引发的CRH期间,F0F1 ATP合酶受到抑制剂蛋白IF(1)的不同调节。记录了10只麻醉山羊的血流动力学参数。在IP之前(Cnp)、CRHnp期间、CRHnp开始后4分钟和6分钟、IP之后(Cprec)、CRHprec期间以及CRHprec后4分钟获取心肌活检样本。测定了F0F1 ATP合酶活性、ATP浓度以及ATP与ADP的比率(ATP/ADP)。与CRHnp相比,IP使CRHprec减弱。F0F1 ATP合酶活性在CRHnp期间短暂增加,在CRHnp后4分钟降低,并在2分钟后恢复至对照水平;在IP之后(Cprec)较低,并且在CRHprec期间及之后没有变化。所有这些活性变化均由IF1调节。在CRHnp期间,与Cnp相比,ATP浓度和ATP/ADP降低,并在6分钟后开始升高。在Cprec期间,这两个参数均短暂降低,但在CRHprec期间及之后升高。因此,在CRHnp期间,F0F1 ATP合酶活性短暂增加,然后显著降低。该酶的短暂抑制可能解释了为什么几秒钟的闭塞不会诱导IP。IP之后,F0F1 ATP合酶活性减弱,并且不受随后15秒闭塞的影响,后者诱导了减弱的CRHprec。这些结果表明,缺血后对F0F1 ATP合酶活性的长期抑制可能是预处理心脏的一个特征。预处理后ATP浓度的增加与先前关于细胞质ATP酶ATP水解减少的报道一致。