Kahles H, Schäfer W, Lick T, Junggeburth J, Kochsiek K
Basic Res Cardiol. 1986 May-Jun;81(3):258-66. doi: 10.1007/BF01907408.
In 15 mongrel open chest dogs oxidative myocardial carbohydrate utilization was stimulated by activation of pyruvatedehydrogenase with S-(4)-hydroxyphenylglycine (HPG) or by inhibition of lipolysis with N(6)-allyl-N(6)-cyclohexyladenosine (PAA). HPG and PAA shifted cardiac respiratory quotients (RQ) from 0.83 to 0.89 and 0.99, respectively. Oxygen extraction ratio of lactate was significantly increased by both interventions. Arterial nonesterified fatty acids (NEFA) concentration decreased significantly only by PAA. The oxygen saving potency of both interventions was quantified over a wide hemodynamic range by comparing the directly measured myocardial oxygen consumption (MVO2) with the myocardial energy requirements calculated from its hemodynamic determinants according to the Bretschneider formula during base conditions and beta-stimulation. Inhibition of peripheral lipolysis with PAA reduced MVO2 by 14%, enzyme activation with HPG by 8%. The results show that the efficiency of the myocardial energy supply can be influenced by manipulation of the oxidative substrate metabolism.
在15只杂种犬开胸实验中,通过用S-(4)-羟基苯甘氨酸(HPG)激活丙酮酸脱氢酶或用N(6)-烯丙基-N(6)-环己基腺苷(PAA)抑制脂肪分解来刺激心肌碳水化合物的氧化利用。HPG和PAA分别使心脏呼吸商(RQ)从0.83变为0.89和0.99。两种干预措施均显著提高了乳酸的氧摄取率。仅PAA使动脉非酯化脂肪酸(NEFA)浓度显著降低。通过比较基础状态和β刺激时直接测量的心肌耗氧量(MVO2)与根据布雷tschneider公式由其血流动力学决定因素计算出的心肌能量需求,在较宽的血流动力学范围内对两种干预措施的氧节省能力进行了量化。用PAA抑制外周脂肪分解使MVO2降低了14%,用HPG激活酶使MVO2降低了8%。结果表明,通过操纵氧化底物代谢可以影响心肌能量供应的效率。