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首页> 外文期刊>BioMed research international >Myeloperoxidase-Related Chlorination Activity Is Positively Associated with Circulating Ceruloplasmin in Chronic Heart Failure Patients: Relationship with Neurohormonal, Inflammatory, and Nutritional Parameters
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Myeloperoxidase-Related Chlorination Activity Is Positively Associated with Circulating Ceruloplasmin in Chronic Heart Failure Patients: Relationship with Neurohormonal, Inflammatory, and Nutritional Parameters

机译:慢性心力衰竭患者与髓过氧化物酶相关的氯化活性与循环铜蓝蛋白呈正相关:与神经激素,炎症和营养参数的关系

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摘要

Rationale. Heart failure (HF) is accompanied by the development of an imbalance between oxygen- and nitric oxide-derived free radical production leading to protein nitration. Both chlorinating and peroxidase cycle of Myeloperoxidase (MPO) contribute to oxidative and nitrosative stress and are involved in tyrosine nitration of protein. Ceruloplasmin (Cp) has antioxidant function through its ferroxidase I (FeOxI) activity and has recently been proposed as a physiological defense mechanism against MPO inappropriate actions.Objective. We investigated the relationship between plasma MPO-related chlorinating activity, Cp and FeOxI, and nitrosative stress, inflammatory, neurohormonal, and nutritional biomarkers in HF patients.Methods and Results. In chronic HF patients (n=81, 76±9 years, NYHA Class II (26); Class III (29); Class IV (26)) and age-matched controls (n=17, 75±11 years, CTR), plasma MPO chlorinating activity, Cp, FeOxI, nitrated protein, free Malondialdehyde, BNP, norepinephrine, hsCRP, albumin, and prealbumin were measured. Plasma MPO chlorinating activity, Cp, BNP, norepinephrine, and hsCRP were increased in HF versus CTR. FeOxI, albumin, and prealbumin were decreased in HF. MPO-related chlorinating activity was positively related to Cp (r= 0.363,P<0.001), nitrated protein, hsCRP, and BNP and inversely to albumin.Conclusions. Plasma MPO chlorinated activity is increased in elderly chronic HF patients and positively associated with Cp, inflammatory, neurohormonal, and nitrosative parameters suggesting a role in HF progression.
机译:基本原理。心力衰竭(HF)伴随着由氧和一氧化氮衍生的自由基产生之间的不平衡发展,导致蛋白质硝化。髓过氧化物酶(MPO)的氯化和过氧化物酶循环都有助于氧化和亚硝化应激,并参与蛋白质的酪氨酸硝化。铜蓝蛋白(Cp)通过其铁氧化物酶I(FeOxI)活性具有抗氧化功能,最近被提出作为针对MPO不适当作用的生理防御机制。我们调查了HF患者血浆MPO相关的氯化活性,Cp和FeOxI与亚硝化应激,炎症,神经激素和营养生物标志物之间的关系。方法和结果。在慢性HF患者(n = 81,76±9岁,NYHA II级(26); III级(29); IV级(26))和年龄匹配的对照组(n = 17,75±11岁,CTR)测定血浆MPO的氯化活性,Cp,FeOxI,硝化蛋白,游离丙二醛,BNP,去甲肾上腺素,hsCRP,白蛋白和前白蛋白。与CTR相比,HF的血浆MPO氯化活性,Cp,BNP,去甲肾上腺素和hsCRP升高。 HF中FeOxI,白蛋白和前白蛋白降低。 MPO相关的氯化活性与Cp(r = 0.363,P <0.001),硝化蛋白,hsCRP和BNP呈正相关,与白蛋白呈反相关。老年慢性HF患者血浆MPO的氯化活性增加,并与Cp,炎性,神经激素和亚硝化参数正相关,提示其在HF进展中起作用。

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