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在24小时胰岛素输注期间,血浆脂联素略有下降,但在使用阿西莫司抑制脂肪分解后,血浆脂联素并未下降。

Plasma adiponectin is modestly decreased during 24-hour insulin infusion but not after inhibition of lipolysis by Acipimox.

作者信息

Dullaart R P F, Riemens S C, Meinardi J R, Wolffenbuttel B H R, Sluiter W J

机构信息

Department of Endocrinology, Groningen University Medical Center, The Netherlands.

出版信息

Scand J Clin Lab Invest. 2005;65(6):523-31. doi: 10.1080/00365510500209090.

Abstract

OBJECTIVE

Plasma adiponectin is associated with insulin resistance and atherosclerosis. Adiponectin expression in adipose tissue is up-regulated by peroxisome proliferator-activated receptor (PPAR)-gamma agonist treatment and its plasma level may be affected by insulin. We tested the hypothesis that prolonged exogenous insulin infusion decreases plasma adiponectin, and examined whether a possible effect of insulin on plasma adiponectin is attributable to inhibition of lipolysis.

MATERIAL AND METHODS

The effect of insulin infusion on plasma adiponectin (Linco enzyme-linked immunosorbent assay) was evaluated during a 24-h moderately hyperinsulinemic clamp (8.3 microU kg(-1) s(-1)) in 8 male type 2 diabetic patients and in 8 healthy men. On a separate day, acipimox (250 mg/4 h for 24 h) was administered to inhibit lipolysis. Insulin and acipimox were administered in random order with 1 week between study days.

RESULTS

In type 2 diabetic patients, insulin infusion decreased plasma adiponectin from 7.74+/-2.53 mg/l to 6.76+/-2.41 mg/l after 24 h (p<0.05). In healthy subjects, the change in plasma adiponectin after 24 h of insulin was not significant (8.10+/-2.76 and 7.55+/-2.41 mg/l at baseline and after 24 h of insulin, respectively). The change in plasma adiponectin after 24 h insulin in healthy subjects was not different from the change in diabetic patients. Plasma adiponectin did not decrease after 24 h acipimox administration in either group (type 2 diabetic patients: 6.84+/-2.19 and 6.54+/-2.93 mg/l at baseline and after 24 h, respectively (NS); healthy subjects; 7.35+/-2.52 and 8.31+/-3.37 mg/l, at baseline and after 24 h, respectively (NS)). When the results from diabetic and healthy subjects were combined, the decrease in plasma adiponectin after 24 h of insulin infusion (-0.76+/-1.08 mg/l, equivalent to a -9% change from baseline, p<0.05) was different (p = 0.05) from the change after 24 h acipimox (+0.33+/-1.74 mg/l, equivalent to a +4% change from baseline). Plasma free fatty acids decreased during insulin infusion (p<0.01 for both groups after 24 h) as well as in response to acipimox (p<0.05 for healthy subjects; p<0.01 type 2 diabetic patients after 24 h). After administration of acipimox, plasma insulin did not change in either group.

CONCLUSIONS

Plasma adiponectin is modestly decreased during 24 h of insulin infusion. It is unlikely that this response to exogenous insulin is attributable to inhibition of lipolysis, since plasma adiponectin did not decrease after acipimox.

摘要

目的

血浆脂联素与胰岛素抵抗和动脉粥样硬化相关。过氧化物酶体增殖物激活受体(PPAR)-γ激动剂治疗可上调脂肪组织中脂联素的表达,其血浆水平可能受胰岛素影响。我们检验了长期外源性胰岛素输注会降低血浆脂联素这一假设,并研究了胰岛素对血浆脂联素的可能作用是否归因于对脂解的抑制。

材料与方法

在8名男性2型糖尿病患者和8名健康男性中,于24小时适度高胰岛素钳夹(8.3微单位·千克⁻¹·秒⁻¹)期间评估胰岛素输注对血浆脂联素(Linco酶联免疫吸附测定法)的影响。在另一天,给予阿昔莫司(250毫克/4小时,共24小时)以抑制脂解。胰岛素和阿昔莫司以随机顺序给药,研究日之间间隔1周。

结果

在2型糖尿病患者中,胰岛素输注24小时后血浆脂联素从7.74±2.53毫克/升降至6.76±2.41毫克/升(p<0.05)。在健康受试者中,胰岛素输注24小时后血浆脂联素的变化不显著(基线时和胰岛素输注24小时后分别为8.10±2.76毫克/升和7.55±2.41毫克/升)。健康受试者胰岛素输注24小时后血浆脂联素的变化与糖尿病患者的变化无差异。两组在给予阿昔莫司24小时后血浆脂联素均未降低(2型糖尿病患者:基线时和24小时后分别为6.84±2.19毫克/升和6.54±2.93毫克/升(无显著性差异);健康受试者:基线时和24小时后分别为7.35±2.52毫克/升和8.31±3.37毫克/升(无显著性差异))。当将糖尿病患者和健康受试者的结果合并时,胰岛素输注24小时后血浆脂联素的降低(-0.76±1.08毫克/升,相当于相对于基线变化-9%,p<0.05)与阿昔莫司给药24小时后的变化(+0.33±1.74毫克/升,相当于相对于基线变化+4%)不同(p = 0.05)。胰岛素输注期间血浆游离脂肪酸降低(两组24小时后均p<0.01),对阿昔莫司的反应也降低(健康受试者p<0.05;2型糖尿病患者24小时后p<0.01)。给予阿昔莫司后,两组血浆胰岛素均未改变。

结论

胰岛素输注24小时期间血浆脂联素略有降低。对外源性胰岛素的这种反应不太可能归因于对脂解的抑制,因为给予阿昔莫司后血浆脂联素并未降低。

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