Ostadal B, Ostadalova I, Dhalla N S
Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Physiol Rev. 1999 Jul;79(3):635-59. doi: 10.1152/physrev.1999.79.3.635.
Hypoxic states of the cardiovascular system are undoubtedly associated with the most frequent diseases of modern times. They originate as a result of disproportion between the amount of oxygen supplied to the cardiac cell and the amount actually required by the cell. The degree of hypoxic injury depends not only on the intensity and duration of the hypoxic stimulus, but also on the level of cardiac tolerance to oxygen deprivation. This variable changes significantly during phylogenetic and ontogenetic development. The heart of an adult poikilotherm is significantly more resistant as compared with that of the homeotherms. Similarly, the immature homeothermic heart is more resistant than the adult, possibly as a consequence of its greater capability for anaerobic glycolysis. Tolerance of the adult myocardium to oxygen deprivation may be increased by pharmacological intervention, adaptation to chronic hypoxia, or preconditioning. Because the immature heart is significantly more dependent on transsarcolemmal calcium entry to support contraction, the pharmacological protection achieved with drugs that interfere with calcium handling is markedly altered. Developing hearts demonstrated a greater sensitivity to calcium channel antagonists; a dose that induces only a small negative inotropic effect in adult rats stops the neonatal heart completely. Adaptation to chronic hypoxia results in similarly enhanced cardiac resistance in animals exposed to hypoxia either immediately after birth or in adulthood. Moreover, decreasing tolerance to ischemia during early postnatal life is counteracted by the development of endogenous protection; preconditioning failed to improve ischemic tolerance just after birth, but it developed during the early postnatal period. Basic knowledge of the possible improvements of immature heart tolerance to oxygen deprivation may contribute to the design of therapeutic strategies for both pediatric cardiology and cardiac surgery.
心血管系统的缺氧状态无疑与现代最常见的疾病相关。它们是由于供应给心肌细胞的氧气量与细胞实际所需氧气量之间的不均衡而产生的。缺氧损伤的程度不仅取决于缺氧刺激的强度和持续时间,还取决于心脏对缺氧的耐受水平。在系统发育和个体发育过程中,这个变量会发生显著变化。成年变温动物的心脏与恒温动物的心脏相比,具有更强的抵抗力。同样,未成熟的恒温动物心脏比成年心脏更具抵抗力,这可能是因为其无氧糖酵解能力更强。成年心肌对缺氧的耐受性可通过药物干预、适应慢性缺氧或预处理来提高。由于未成熟心脏对跨肌膜钙内流以支持收缩的依赖性更强,因此使用干扰钙处理的药物所实现的药理保护作用会明显改变。发育中的心脏对钙通道拮抗剂表现出更高的敏感性;在成年大鼠中仅引起轻微负性肌力作用的剂量会使新生心脏完全停搏。适应慢性缺氧会使在出生后立即或成年期暴露于缺氧环境的动物的心脏抵抗力同样增强。此外,出生后早期对缺血耐受性的降低会被内源性保护机制的发展所抵消;预处理在出生后即刻并不能提高缺血耐受性,但在出生后早期会逐渐发展。了解未成熟心脏对缺氧耐受性可能的改善的基本知识,可能有助于为小儿心脏病学和心脏外科设计治疗策略。