Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Sleep Breath. 2010 Dec;14(4):291-8. doi: 10.1007/s11325-010-0368-x. Epub 2010 Jul 14.
Cells sense oxygen availability using not only the absolute value for cellular oxygen in regard to its energetic and metabolic functions, but also the gradient from the cell surface to the lowest levels in the mitochondria. Signals are used for regulatory purposes locally as well as in the generation of cellular, tissue, and humoral remodeling. Lowered oxygen availability (hypoxia) is theoretically important in the consideration of pharmacology because (1) hypoxia can alter cellular function and thereby the therapeutic effectiveness of the agent, (2) therapeutic agents may potentiate or protect against hypoxia-induced pathology, (3) hypoxic conditions may potentiate or mitigate drug-induced toxicity, (4) hypoxia may alter drug metabolism and thereby therapeutic effectiveness, and (5) therapeutic agents might alter the relative coupling of blood flow and energy metabolism in an organ. The prototypic biochemical effect of hypoxia is related to its known role as a cofactor in a number of enzymatic reactions, e.g., oxidases and oxygenases, which are affected independently from the bioenergetic effect of low oxygen on energetic functions. The cytochrome P-450 family of enzymes is another example. Here, there is a direct effect of oxygen availability on the conformation of the enzyme, thereby altering the metabolism of drug substrates. Indirectly, the NADH/NAD+ ratio is increased with 10% inspired oxygen, leading not only to reduced oxidation of ethanol but also to reduction of azo- and nitro-compounds to amines and disulfides to sulfhydryls. With chronic hypoxia, many of these processes are reversed, suggesting that hypoxia induces the drug-metabolizing systems. Support for this comes from observations that hypoxia can induce the hypoxic inducible factors which in turn alters transcription and function of some but not all cytochrome P-450 isoforms. Hypoxia is identified as a cofactor in cancer expression and metastatic potential. Thus, the effects of hypoxia play an important role in pharmacology, and the signaling pathways that are affected by hypoxia could become new targets for novel therapy or avenues for prevention.
细胞不仅通过细胞内氧的绝对值来感知氧气供应情况,还通过细胞表面到线粒体最低水平的氧梯度来感知氧气供应情况,以满足其能量和代谢功能。信号用于局部的调节目的,以及细胞、组织和体液重塑的产生。氧气供应不足(缺氧)在药理学考虑中具有理论重要性,原因如下:(1)缺氧可以改变细胞功能,从而影响药物的治疗效果;(2)治疗药物可能增强或预防缺氧引起的病理变化;(3)缺氧条件可能增强或减轻药物引起的毒性;(4)缺氧可能改变药物代谢,从而影响治疗效果;(5)治疗药物可能改变器官中血流和能量代谢的相对耦合。缺氧的典型生化效应与其在许多酶反应中的已知作用有关,例如氧化酶和加氧酶,这些反应独立于低氧对能量功能的生物能量效应。细胞色素 P-450 酶家族就是另一个例子。在这里,氧气供应直接影响酶的构象,从而改变药物底物的代谢。间接的,10%吸入氧气会增加 NADH/NAD+的比例,不仅导致乙醇氧化减少,还导致偶氮和硝基化合物还原为胺,二硫化物还原为巯基。在慢性缺氧的情况下,许多这些过程会被逆转,这表明缺氧会诱导药物代谢系统。这一观点得到了观察结果的支持,即缺氧可以诱导缺氧诱导因子,进而改变一些但不是所有细胞色素 P-450 同工型的转录和功能。缺氧被确定为癌症表达和转移潜能的辅助因子。因此,缺氧的影响在药理学中起着重要作用,受缺氧影响的信号通路可能成为新的治疗靶点或预防途径。