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哪种心脏利钠肽对治疗充血性心力衰竭、肾衰竭和癌症最有效?

Which of the cardiac natriuretic peptides is most effective for the treatment of congestive heart failure, renal failure and cancer?

作者信息

Vesely David L

机构信息

University of South Florida Cardiac Hormone Center and James A Haley Veteran's Medical Center, Tampa, Florida, USA.

出版信息

Clin Exp Pharmacol Physiol. 2006 Mar;33(3):169-76. doi: 10.1111/j.1440-1681.2006.04344.x.

Abstract

Cardiac natriuretic peptides consist of a family of six peptide hormones that are synthesised by three separate genes and then stored as three separate prohormones (i.e. 126 amino acid atrial natriuretic peptide (ANP), 108 amino acid B-type natriuretic peptide (BNP) and 103 amino acid C-type natriuretic peptide (CNP) prohormones). The ANP prohormone contains four peptide hormones: long-acting natriuretic peptide (LANP), vessel dilator, kaliuretic peptide and ANP. 2. Currently, the only natriuretic peptide available commercially to treat congestive heart failure (CHF) is BNP (Nesiritide/Natrecor; SCIOS, Sunnyvale, CA, USA), which causes a small increase in the urine volume of 90 38 mL/h compared with 67 27 mL/h and no significant natriuresis, but has beneficial haemodynamic effects in acute CHF individuals. These haemodynamic effects probably contribute to the side-effects of BNP in patients with acute CHF with a 27% incidence of hypotension and possibly to 22% worsening of renal function, defined as an increase in serum creatinine of 0.5 mg/dL, associated with a worse prognosis. A review of clinical trials suggests a twofold increased risk of death at 30 days post-nesiritide treatment, a finding that needs further investigation. 3. The best of the natriuretic peptides for treating chronic CHF is the vessel dilator, which increases urinary flow up to 13-fold and sodium excretion up to fourfold, without the previously mentioned side-effects. The natriuretic and diuretic effects of vessel dilators last 6 h, which would allow them to be used on a four times per day basis in treating chronic CHF. 4. Atrial natriuretic peptide does not cause significant improvement in acute renal failure (ARF) in humans. The only natriuretic peptide that significantly improves ARF is the vessel dilator. Even when ARF has been established for 2 days before treatment in an ischaemic ARF animal model, vessel dilator decreases serum creatinine from 8.2 0.5 to 0.98 0.12 mg/dL in 6 days. At day 6 of ARF, mortality decreases to 14% (from 88%) without the vessel dilator. After 6 days of treatment with the vessel dilator, the proximal and distal tubules regenerate. 5. In cancer, vessel dilator, LANP, kaliuretic peptide and ANP at 1 mmol/L, decrease up to 97% of human breast, pancreatic and prostate adenocarcinoma cells, as well as small cell and squamous cell lung cancer cells within 24 h. In vivo, vessel dilator, LANP and kaliuretic peptide completely stop the growth of human pancreatic adenocarcinomas in athymic mice and decrease their tumour volume by 49, 28 and 11%, respectively in 1 week.

摘要

心脏利钠肽由六种肽类激素组成的一个家族,它们由三个不同的基因合成,然后作为三种不同的前激素储存(即126个氨基酸的心房利钠肽(ANP)、108个氨基酸的B型利钠肽(BNP)和103个氨基酸的C型利钠肽(CNP)前激素)。ANP前激素包含四种肽类激素:长效利钠肽(LANP)、血管扩张肽、利钾肽和ANP。2. 目前,唯一可用于商业治疗充血性心力衰竭(CHF)的利钠肽是BNP(奈西立肽/心钠素;SCIOS,美国加利福尼亚州桑尼维尔),与67±27 mL/h相比,它使尿量小幅增加至90±38 mL/h,且无明显利钠作用,但对急性CHF患者有有益的血流动力学效应。这些血流动力学效应可能导致急性CHF患者使用BNP出现副作用,低血压发生率为27%,肾功能可能恶化22%,定义为血清肌酐升高0.5 mg/dL,且预后较差。对临床试验的综述表明,奈西立肽治疗后30天死亡风险增加两倍这一发现需要进一步研究。3. 治疗慢性CHF的最佳利钠肽是血管扩张肽,它可使尿流量增加至13倍,钠排泄增加至4倍,且无上述副作用。血管扩张肽的利钠和利尿作用持续6小时,这使其可用于每日四次治疗慢性CHF。4. 心房利钠肽对人类急性肾衰竭(ARF)无显著改善作用。唯一能显著改善ARF的利钠肽是血管扩张肽。即使在缺血性ARF动物模型中治疗前ARF已确立2天,血管扩张肽仍可在6天内使血清肌酐从8.2±0.5降至0.98±0.12 mg/dL。在ARF第6天,未使用血管扩张肽时死亡率降至14%(之前为88%)。用血管扩张肽治疗6天后,近端和远端肾小管再生。5. 在癌症中,1 mmol/L的血管扩张肽、LANP、利钾肽和ANP可在24小时内使人类乳腺癌、胰腺癌和前列腺癌细胞以及小细胞和鳞状细胞肺癌细胞减少多达97%。在体内,血管扩张肽、LANP和利钾肽可完全阻止无胸腺小鼠体内人类胰腺腺癌的生长,并在1周内分别使肿瘤体积减少49%、28%和11%。

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