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Adrenal gland‐released vasostatin‐I is a myocardial depressant factor

机译:肾上腺释放的vasostatin-i是一种心肌抑郁症因子

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摘要

Pheochromocytoma crisis is an exceptional consequence of the release of storage vesicles of the adrenal medulla. It is complicated by fulminant adrenergic myocarditis. It offers a unique opportunity to detect inotropic negative factors from neuroendocrine origin. Our objectives were (a) to describe a pheochromocytoma crisis, (b) to investigate in vivo myocardial depressant activities for the N‐terminal 1‐76 Chromogranin A‐derived peptide, vasostatin‐I (VS‐I). A patient with a pheochromocytoma crisis was treated, including extracorporeal membrane oxygenation, until mass resection. Plasma concentrations of VS‐I were time‐dependently assessed with a specific immunoassay; correlations with invasive cardiovascular parameters were investigated. Increased VS‐I concentrations were observed over 7 days until tumour resection. VS‐I concentrations correlated positively with Chromogranin A levels, negatively with cardiac output and left ventricular stroke work index, but not with heart rate. This case illustrates the pharmacokinetics of VS‐I in a pheochromocytoma crisis. It highlights myocardial depressant activity for this peptide at high concentrations.
机译:Pheochromocytoma危机是肾上腺髓质储存囊泡释放的特殊后果。令人兴奋的肾上腺素能心肌炎是复杂的。它提供了检测神经内分泌起源的各渗透性负面因素的独特机会。我们的目标是(a)描述嗜铬细胞瘤危机,(b)在N-末端1-76 Chromogranin A衍生的肽,Vasostatin-I(Vs-I)中调查体内心肌抑制活性。处理具有噬菌体细胞瘤危机的患者,包括体外膜氧合,直至大规模切除。用特定的免疫测定依赖性评估VS-1的血浆浓度;研究了与侵袭性心血管参数的相关性。在7天内观察到增加VS-I浓度直至肿瘤切除。 VS-I浓度与Chormogranin A水平正相关,对心输出和左心室中风工作指数负面相关,但不是心率。这种情况说明了VS-I中的药代动力学在嗜铬细胞瘤危机中。它突出了高浓度的这种肽的心肌抑制活性。

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