Influence of ALDH2 Glu504Lys polymorphism on nitroglycerin response in chronic heart failure and involvement of Calcitonin Gene Related Peptide (CGRP)

被引:13
|
作者
Peng, Li-Ming [1 ]
Chen, Xiao-Ping [1 ]
Sun, Ji [1 ]
Guo, Yi-Jie [1 ]
Li, Ling [1 ]
Mo, Long
Xie, Wei
Li, Yuan-Jian [1 ]
Yang, Tian-Lun
Li, Chuan-Chang [2 ]
机构
[1] Cent S Univ, Dept Pharmacol, Sch Pharmaceut Sci, Changsha 410078, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Cardiol, Changsha 410078, Hunan, Peoples R China
基金
美国国家科学基金会;
关键词
nitroglycerin (GIN); mitochondrial aldehyde dehydrogenase (ALDH2); genetic polymorphism; calcitonin gene related peptide (CGRP); chronic heart failure (CHF); INDUCED MIGRAINE ATTACK; ALDEHYDE DEHYDROGENASE-2; NITRIC-OXIDE; XANTHINE OXIDOREDUCTASE; INTRAVENOUS NITROGLYCERIN; GLYCERYL TRINITRATE; NITRATE TOLERANCE; RELEASE; VASODILATOR; BIOTRANSFORMATION;
D O I
10.5414/CP201635
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The aim of this study was to investigate whether the neuropeptide calcitonin gene related peptide (CGRP) contributes to nitroglycerin (GTN) response in patients with chronic heart failure (CHF) and the association with the mitochondrial aldehyde dehydrogenase-2 (ALDH2) Glu504Lys (ALDH2*2) polymorphism. Methods: This is a 2-period, placebo-controlled clinical study. An intravenous infusion of saline followed by GIN (20 mu g/min), each for 2 hours, respectively, was given to 49 stable CHF patients. Blood pressure (BP), heart rate (HR) and respiratory rate (RR) were measured at baseline, at 10 min, 30 min, 1.0 h, 1.5 h, and 2.0 h after initiation of saline infusion and initiation of GTN therapy. Blood samples were drawn for the determination of plasma CGRP for 49 patients at baseline, and at 2.0 h after initiation of saline and GTN infusion, respectively. Global clinical status of the patients was evaluated. Left ventricular ejection (LVEF), left ventricular end-diastolic volume (LVEDV), stroke volume (SV) and cardiac output (CO) were measured with 2D echocardiography with Simpson's biplane method (Pillip HP sonos 5500) by the same investigator at baseline and at 2.0 h after initiation of saline and GTN infusion. Results: Systolic blood pressure (SBP), diastolic blood pressure (DBP), and left ventricular end-diastolic volume (LVEDV) were decreased, while left ventricular ejection fraction (LVEF) was increased at the end of GIN infusion (p < 0.001, respectively). Saline infusion showed no hemodynamic effects. At the end of GIN infusion, ALDH2*1/*1 homozygous patients showed higher degrees of both the absolute decrease in SBP (ASBP) (p < 0.001) and increase in LVEF (p < 0.001) than carriers of the ALDH2*2 allele. Mean plasma concentration of CGRP was increased after GIN infusion (p < 0.001), but not changed after saline infusion (p > 0.05). Changes in plasma concentration of CGRP correlated positively with the improvement in LVEF (r = 0.400, p = 0.004), while correlated negatively with changes in SBP (r 0.300, p = 0.036) and LVEDV (r = 0.290, p = 0.043). Conclusions: ALDH2*2 polymorphism is associated with contributions of CGRP to GTN response in CHF patients.
引用
收藏
页码:701 / 711
页数:11
相关论文
共 20 条
  • [1] Involvement of Anandamide Transporter in Calcitonin Gene-related Peptide Expression Stimulated by Nitroglycerin and Influence of ALDH2 Glu504Lys Polymorphism
    Peng, Li-Ming
    Chen, Xiao-Ping
    Shi, Rui-Zheng
    Chen, Lei
    Li, Yuan-Jian
    Yang, Tian-Lun
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2014, 64 (05) : 460 - 464
  • [2] Evidence for involvement of calcitonin gene-related peptide in nitroglycerin response and association with mitochondrial aldehyde dehydrogenase-2 (ALDH2) Glu504Lys polymorphism
    Guo, Ren
    Chen, Xiao-Ping
    Guo, Xin
    Chen, Lei
    Li, Dai
    Peng, Jun
    Li, Yuan-Jian
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 52 (11) : 953 - 960
  • [3] Mitochondrial aldehyde dehydrogenase (ALDH2) Glu504Lys polymorphism is responsible for variation in efficacy of sublingual nitroglycerin
    Jin, Li
    Li, Yifeng
    Zhang, Dandan
    Jin, Wei
    Yu, Jinde
    Nebert, Daniel W.
    Harrison, Donald C.
    Huang, Wei
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2006, 30 (09) : 92A - 92A
  • [4] Mitochondrial aldehyde dehydrogenase-2 (ALDH2) Glu504Lys polymorphism contributes to the variation in efficacy of sublingual nitroglycerin
    Li, YF
    Zhang, DD
    Jin, W
    Shao, CH
    Yan, PR
    Xu, CJ
    Sheng, HH
    Liu, Y
    Yu, JD
    Xie, YJ
    Zhao, YN
    Lu, DR
    Nebert, DW
    Harrison, DC
    Huang, W
    Jin, L
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (02): : 506 - 511
  • [5] Association between Glu504Lys Polymorphism of ALDH2 Gene and Cancer Risk: A Meta-Analysis
    Cai, Qiang
    Wu, Jian
    Cai, Qu
    Chen, Er-Zhen
    Jiang, Zhao-Yan
    [J]. PLOS ONE, 2015, 10 (02):
  • [6] ALDEHYDE DEHYDROGENASE-2 (ALDH2) GLU504LYS POLYMORPHISM AFFECTS STROKE IN A CHINESE POPULATION
    Liu, Xin
    Liu, Lisheng
    Wang, Xingyu
    [J]. JOURNAL OF HYPERTENSION, 2018, 36 : E72 - E72
  • [7] Association between ALDH2 Glu504Lys polymorphism and colorectal cancer risk: a meta-analysis
    Jiang Xinhua
    Zhao Yanfei
    [J]. AFRICAN HEALTH SCIENCES, 2017, 17 (01) : 108 - 115
  • [8] The aldehyde dehydrogenase 2 (ALDH2) Glu504Lys polymorphism interacts with alcohol drinking in the risk of stomach cancer
    Matsuo, Keitaro
    Oze, Isao
    Hosono, Satoyo
    Ito, Hidemi
    Watanabe, Miki
    Ishioka, Kuka
    Ito, Seiji
    Tajika, Masahiro
    Yatabe, Yasushi
    Niwa, Yasumasa
    Yamao, Kenji
    Nakamura, Shigeo
    Tajima, Kazuo
    Tanaka, Hideo
    [J]. CARCINOGENESIS, 2013, 34 (07) : 1510 - 1515
  • [9] Association of a Missense ALDH2 Single Nucleotide Polymorphism (Glu504Lys) With Benign Prostate Hyperplasia in a Korean Population
    Seok, Hosik
    Yoo, Koo Han
    Kim, Young Ock
    Chung, Joo-Ho
    [J]. INTERNATIONAL NEUROUROLOGY JOURNAL, 2013, 17 (04) : 168 - 173
  • [10] Aldehyde dehydrogenase 2 (ALDH2) Glu504Lys polymorphism is associated with hypertension risk in Asians: a meta-analysis
    Jia, Kui
    Wang, Honglei
    Dong, Pingshuan
    [J]. INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (07): : 10767 - 10772