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脂联素在心力衰竭中是旁观者还是中介?这种好心的脂肪因子在衰老和心血管疾病中的复杂关系。

Is adiponectin a bystander or a mediator in heart failure? The tangled thread of a good-natured adipokine in aging and cardiovascular disease.

机构信息

Division of Geriatric Medicine, Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

Heart Fail Rev. 2010 Sep;15(5):457-66. doi: 10.1007/s10741-010-9159-5.

Abstract

Adiponectin is an adipose tissue-derived adipokine abundant in human plasma. Increasing evidence from experimental studies suggests that adiponectin plays a protective role in the cardiovascular system. However, epidemiological studies revealed that high levels of adiponectin were associated with increased mortality and severity of congestive heart failure. Furthermore, several prospective studies indicated that high levels of adiponectin were positively correlated with increased total and cardiovascular disease mortality in the elderly. These results are completely opposite to our expectation based on the beneficial effects of adiponectin. Clinical observations demonstrated that plasma adiponectin levels were positively associated with B-type natriuretic peptide levels. Clinical and experimental studies indicated that the administration of atrial natriuretic peptide enhanced adiponectin production. It is still controversial whether increased adiponectin production is a bystander or a key mediator in the development of heart failure. However, recent investigations strongly suggest that increased adiponectin production in patients with heart failure is a part of compensatory mechanisms against oxidative stress and inflammation. In addition, complicated "adiponectin resistance" will accelerate a counter-regulatory increase in adiponectin in patients with advanced heart failure, although direct evidence that patients with heart failure have "adiponectin resistance" is still lacking. Increased adiponectin production might contribute, at least in part, to the metabolic and structural remodeling of the failing heart via activation of AMP-activated protein kinase and induction of cyclooxygenase-2. Further investigation is needed to clarify the exact role of increased adiponectin production under pathophysiological conditions.

摘要

脂联素是一种丰富存在于人类血浆中的脂肪组织来源的脂肪因子。越来越多的实验研究证据表明,脂联素在心血管系统中发挥保护作用。然而,流行病学研究表明,高水平的脂联素与死亡率增加和充血性心力衰竭的严重程度相关。此外,几项前瞻性研究表明,高水平的脂联素与老年人总死亡率和心血管疾病死亡率的增加呈正相关。这些结果与我们基于脂联素有益作用的预期完全相反。临床观察表明,血浆脂联素水平与 B 型利钠肽水平呈正相关。临床和实验研究表明,心房利钠肽的给药增强了脂联素的产生。增加的脂联素产生是心力衰竭发展中的旁观者还是关键介质仍存在争议。然而,最近的研究强烈表明,心力衰竭患者中脂联素产生的增加是对抗氧化应激和炎症的代偿机制的一部分。此外,尽管仍缺乏心力衰竭患者存在“脂联素抵抗”的确凿证据,但复杂的“脂联素抵抗”会加速心力衰竭患者中脂联素的代偿性增加。增加的脂联素产生可能至少部分通过激活 AMP 激活的蛋白激酶和诱导环氧化酶-2,有助于衰竭心脏的代谢和结构重塑。需要进一步的研究来阐明在病理生理条件下增加的脂联素产生的确切作用。

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