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肥胖和糖尿病患者的血小板聚集:与瘦素水平的关联。

Platelet aggregation in obese and diabetic subjects: association with leptin level.

作者信息

Sugiyama Chiyo, Ishizawa Masayoshi, Kajita Kazuo, Morita Hiroyuki, Uno Yoshihiro, Matsubara Kenji, Matsumoto Masami, Ikeda Takahide, Ishizuka Tatsuo

机构信息

Departments of General Internal Medicine, Gifu University Graduate School of Medicine, Yanagido 1-1, Gifu 501-1194, Japan.

出版信息

Platelets. 2007 Mar;18(2):128-34. doi: 10.1080/09537100600819115.

Abstract

To clarify the relationship between serum leptin concentration and platelet aggregation mechanism, we investigated serum leptin concentration and agonist-induced platelet aggregation in eight obese subjects and eight non-obese and non-diabetic controls. In addition we also measured them in 15 type 2 diabetic subjects and 17 control subjects. Maximum platelets aggregation rate (MPAR) in control and diabetic subjects by adenosine diphosphate (ADP), collagen and thrombin were measured by aggregometer after pretreatment with 100 ng/ml leptin for 60 min. The MPAR by 0.15 U/ml thrombin stimulation in leptin-treated platelet in the controls was significantly increased compared with that in non-treated platelets, but not by ADP and collagen stimulation. Despite a significantly higher concentration of leptin in obese subjects, agonist-induced platelet aggregation in obese subjects was not different from that in controls. There were no significant differences in serum leptin concentration and MPAR by various agonists between diabetic and control subjects. When MPAR by ADP in the diabetic subjects was divided into two groups (high group: >50%, low group: <50%), the serum leptin concentration in the high group was significantly increased, compared with that in the low group. These results suggest that ADP-induced platelet aggregation may be associated with serum leptin concentration in diabetic subjects, and that leptin-associated platelet aggregation may affect the development of cardiovascular complications in obese and diabetic subjects.

摘要

为阐明血清瘦素浓度与血小板聚集机制之间的关系,我们对8名肥胖受试者以及8名非肥胖且非糖尿病的对照者,研究了血清瘦素浓度和激动剂诱导的血小板聚集情况。此外,我们还对15名2型糖尿病受试者和17名对照者进行了检测。在用100 ng/ml瘦素预处理60分钟后,通过凝集仪测量对照者和糖尿病受试者中由二磷酸腺苷(ADP)、胶原蛋白和凝血酶诱导的最大血小板聚集率(MPAR)。与未处理的血小板相比,对照者中经瘦素处理的血小板在0.15 U/ml凝血酶刺激下的MPAR显著升高,但在ADP和胶原蛋白刺激下未升高。尽管肥胖受试者的瘦素浓度显著更高,但肥胖受试者中激动剂诱导的血小板聚集与对照者并无差异。糖尿病受试者和对照者之间,血清瘦素浓度以及各种激动剂诱导的MPAR均无显著差异。当将糖尿病受试者中ADP诱导的MPAR分为两组(高组:>50%,低组:<50%)时,高组的血清瘦素浓度相较于低组显著升高。这些结果表明,在糖尿病受试者中,ADP诱导的血小板聚集可能与血清瘦素浓度有关,并且瘦素相关的血小板聚集可能会影响肥胖和糖尿病受试者心血管并发症的发生发展。

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