首页> 外文期刊>The Japanese journal of physiology >Increased cardiovascular and metabolic tolerance to acute hypoxia in the rat with increased hemoglobin-O(2) affinity induced by Na-cyanate treatment.
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Increased cardiovascular and metabolic tolerance to acute hypoxia in the rat with increased hemoglobin-O(2) affinity induced by Na-cyanate treatment.

机译:对大鼠急性缺氧的心血管和代谢耐受性增加,血红蛋白-O(2)亲和力由氰酸钠引起。

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摘要

Cyanate derivatives such as NaOCN have been known to increase the hypoxia tolerance of animals by increasing the affinity of hemoglobin (Hb) to O(2). To clarify the mechanism of this increase in hypoxia tolerance, we examined changes in metabolic rate and cardiovascular parameters during a hypoxia test in halothane-anesthetized, NaOCN-treated and spontaneously breathing rats (50 mg/kg/d S.C., 10 d). Control animals received saline. The capillary density in the skeletal muscle (sternocleidomastoid muscle), cardiac papillary muscle and medulla oblongata was also examined histologically. The Hb-O(2) affinity index, P(50), decreased from 38 (control rat) to 24 mmHg in NaOCN-treated rats. During hyperoxic gas breathing, the rat treated with NaOCN showed a significantly lower metabolic rate (V(.)O(2), V(.)CO(2)), higher cardiac stroke volume, slower heart rate, lower PvO(2), and lower O(2) extraction ratio than those in control rats. The NaOCN-treated rats exhibited well-maintained arterial blood pressure and a larger cardiac output response to reduction in FIO(2) to 0.10-0.08. The increase in O(2) extraction ratio with reduction in FIO(2) was larger in NaOCN-treated than in control rats. The circulatory and metabolic depressions at FIO(2) 0.05 were effectively attenuated in NaOCN-treated rats. The capillary density of the cardiac muscle and medulla oblongata but not the skeletal muscle was significantly higher in NaOCN-treated rats than in control rats. The greater hypoxia tolerance in NaOCN-treated rats is ascribed to the combined effects of left shift of Hb-O(2) dissociation curve, lower basal V(. )O(2), higher capillary density in the heart, and brain, and other adaptive mechanisms induced probably by prolonged tissue hypoxia.
机译:已知诸如NaOCN之类的氰酸盐衍生物可通过增加血红蛋白(Hb)对O(2)的亲和力来提高动物的耐缺氧性。为了阐明这种耐缺氧性增加的机制,我们在氟烷麻醉,NaOCN处理和自发呼吸的大鼠(50 mg / kg / d S.C.,10 d)进行的缺氧测试中检查了代谢率和心血管参数的变化。对照动物接受盐水。还通过组织学检查了骨骼肌(胸锁乳突肌),心脏乳头肌和延髓中的毛细血管密度。在NaOCN处理的大鼠中,Hb-O(2)亲和力指数P(50)从38(对照大鼠)降至24 mmHg。在高氧气体呼吸期间,用NaOCN治疗的大鼠表现出明显更低的代谢率(V(.O)(2),V(。)CO(2)),较高的心搏量,较慢的心率,较低的PvO(2) ,并且O(2)的提取率低于对照组。 NaOCN治疗的大鼠表现出良好的动脉血压和较大的心输出量,对FIO(2)降低至0.10-0.08。 NaOCN处理的O(2)提取率的增加与FIO(2)的减少相比,在对照组中更大。在NaOCN治疗的大鼠中,FIO(2)0.05处的循环和代谢抑制有效降低。 NaOCN处理的大鼠的心肌和延髓的毛细血管密度,而非骨骼肌的毛细血管密度显着高于对照组。 NaOCN处理的大鼠耐缺氧性更高是由于Hb-O(2)解离曲线左移,基础V(。)O(2)较低,心脏和大脑中较高的毛细血管密度和其他适应性机制可能是由于组织缺氧时间延长所致。

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