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青少年特发性脊柱侧弯中的血小板功能

Platelet function in adolescent idiopathic scoliosis.

作者信息

Kahmann R D, Donohue J M, Bradford D S, White J G, Rao G H

机构信息

Department of Orthopaedic Surgery, University of Minnesota, Minneapolis.

出版信息

Spine (Phila Pa 1976). 1992 Feb;17(2):145-8. doi: 10.1097/00007632-199202000-00005.

Abstract

Recent studies have reported abnormal platelet morphology and function in patients with adolescent idiopathic scoliosis. These abnormalities include increased platelet size and dense body numbers, abnormal aggregation, thromboxane A2 synthesis, serotonin release to adenosine diphosphate and epinephrine stimulus, and decreased myosin-adenosine-triphosphatase-specific activity. It was postulated that a membrane-specific defect in calcium transport may be partially responsible for the abnormalities found. In response to a suggestion in the literature that platelet screening could be clinically useful in scoliosis evaluation as well as in basic research of its pathophysiology, a study was performed to evaluate platelet morphology, biochemistry, and function in patients with adolescent idiopathic scoliosis. Platelets from nine volunteers with adolescent idiopathic scoliosis were compared with cells from a control group of nine patients. No significant differences in measured platelet parameters were noted between adolescent idiopathic scoliosis patients and control groups. Platelets from both groups demonstrated normal aggregation and release patterns with all agents except for a mild decreased aggregation and secretion response to epinephrine. No significant differences were noted in serotonin or adenine nucleotide levels. No significant ultrastructural differences were noted. Earlier findings of an abnormal aggregation and secretion response to adenosine diphosphate, increased numbers of dense bodies, or increased intracellular calcium could not be confirmed. On the contrary, we found normal, if not slightly decreased, numbers of dense bodies per platelet and calcium levels that were not different from controls.

摘要

近期研究报道了青少年特发性脊柱侧凸患者血小板形态和功能异常。这些异常包括血小板体积增大、致密体数量增加、聚集异常、血栓素A2合成异常、对二磷酸腺苷和肾上腺素刺激的5-羟色胺释放异常以及肌球蛋白-三磷酸腺苷特异性活性降低。据推测,钙转运的膜特异性缺陷可能是所发现异常的部分原因。鉴于文献中提出血小板筛查在脊柱侧凸评估及其病理生理学基础研究中可能具有临床应用价值,因此开展了一项研究来评估青少年特发性脊柱侧凸患者的血小板形态、生物化学和功能。将9名青少年特发性脊柱侧凸志愿者的血小板与9名对照组患者的细胞进行比较。青少年特发性脊柱侧凸患者与对照组之间在测量的血小板参数方面未发现显著差异。两组的血小板对所有试剂均表现出正常的聚集和释放模式,只是对肾上腺素的聚集和分泌反应略有降低。5-羟色胺或腺嘌呤核苷酸水平未发现显著差异。超微结构也未发现显著差异。早期关于对二磷酸腺苷的聚集和分泌反应异常、致密体数量增加或细胞内钙增加的研究结果未能得到证实。相反,我们发现每个血小板的致密体数量正常,即便略有减少,且钙水平与对照组无差异。

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