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低磷血症与横纹肌溶解症。

Hypophosphatemia and rhabdomyolysis.

作者信息

Knochel J P, Barcenas C, Cotton J R, Fuller T J, Haller R, Carter N W

出版信息

J Clin Invest. 1978 Dec;62(6):1240-6. doi: 10.1172/JCI109244.

Abstract

Clinical observations suggest that overt rhabdomyolysis may occur if severe hypophosphatemia is superimposed upon a pre-existing subclinical myopathy. To examine this possibility, a subclinical muscle cell injury was induced in 23 dogs by feeding them a phosphorus- and calorie-deficient diet until they lost 30% of their original weight. To induce acute, severe hypophosphatemia in the animals after partial starvation, 17 of the dogs were given large quantities of the same phosphorus-deficient diet in conjunction with an oral carbohydrate supplement, which together provided 140 kcal/kg per day. After phosphorus and caloric deprivation, serum phosphorus and creatine phosphokinase (CPK) activity were normal. Total muscle phosphorus content fell from 28.0+/-1.3 to 26.1+/-2.5 mmol/dg fat-free dry solids. Sodium, chloride, and water contents rose. These changes resembled those observed in patients with subclinical alcoholic myopathy. When studied after 3 days of hyperalimentation, the animals not receiving phosphorus showed weakness, tremulousness, and in some cases, seizures. Serum phosphorus fell, the average lowest value was 0.8 mg/dl (P <0.001). CPK activity rose from 66+/-357 to 695+/-1,288 IU/liter (P <0.001). Muscle phosphorus content fell further to 21.1+/-7.7 mmol/dg fat-free dry solids (P <0.001). Muscle Na and Cl contents became higher (P <0.01). Sections of gracilis muscle showed frank rhabdomyolysis.6 of the 23 phosphorus- and calorie-deprived dogs were also given 140 kal/kg per day but in addition, each received 147 mmol of elemental phosphorus. These dogs consumed their diet avidly and displayed no symptoms. They did not become hypophosphatemic, their CPK remained normal, and derangements of cellular Na, Cl, and H(2)O were rapidly corrected. The gracilis muscle appeared normal histologically in these animals. These data suggest that a subclinical myopathy may set the stage for rhabdomyolysis if acute, severe hypophosphatemia is superimposed. Neither acute hypophosphatemia nor rhabdomyolysis occur if abundant phosphorus is provided during hyperalimentation.

摘要

临床观察表明,如果严重低磷血症叠加在已存在的亚临床肌病之上,可能会发生明显的横纹肌溶解。为了检验这种可能性,对23只狗喂食低磷和低热量饮食,直至体重减轻30%,从而诱导亚临床肌肉细胞损伤。为了在部分饥饿后使动物发生急性、严重低磷血症,给其中17只狗喂食大量相同的低磷饮食,并口服碳水化合物补充剂,两者共同提供每天140千卡/千克的热量。在磷和热量缺乏后,血清磷和肌酸磷酸激酶(CPK)活性正常。肌肉总磷含量从28.0±1.3降至26.1±2.5毫摩尔/克无脂干固体。钠、氯和水含量升高。这些变化与亚临床酒精性肌病患者中观察到的变化相似。在进行3天的肠外营养后进行研究时,未补充磷的动物出现虚弱、震颤,在某些情况下还出现癫痫发作。血清磷下降,平均最低值为0.8毫克/分升(P<0.001)。CPK活性从66±357升至695±1288国际单位/升(P<0.001)。肌肉磷含量进一步降至21.1±7.7毫摩尔/克无脂干固体(P<0.001)。肌肉钠和氯含量升高(P<0.01)。股薄肌切片显示明显的横纹肌溶解。23只接受磷和热量剥夺的狗中有6只也给予每天140千卡/千克,但此外,每只狗还接受147毫摩尔元素磷。这些狗积极进食且未出现症状。它们没有发生低磷血症,CPK保持正常,细胞钠、氯和水的紊乱迅速得到纠正。这些动物的股薄肌在组织学上看起来正常。这些数据表明,如果叠加急性、严重低磷血症,亚临床肌病可能为横纹肌溶解创造条件。如果在肠外营养期间提供充足的磷,则既不会发生急性低磷血症也不会发生横纹肌溶解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8083/371889/404a1189cb83/jcinvest00672-0132-a.jpg

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