Correlation between Akp2 and myocardial fibrosis post myocardial infarction
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Correlation between Akp2 and myocardial fibrosis post myocardial infarction
Journal of Third Military Medical UniversityPages: 1-7(2022)
作者机构:
1.实验研究中心2
2.Chongqing 400016
作者简介:
基金信息:
the General Program of National Natural Science Foundation of China(31800976;81970203);ACCESS Fund of China Heart House - China Cardiovascular Association(2018-CCA-AF-034;ky-2017-07-08)
Correlation between Akp2 and myocardial fibrosis post myocardial infarction. [J/OL]. Journal of Third Military Medical University 1-7(2022)
DOI:
Correlation between Akp2 and myocardial fibrosis post myocardial infarction. [J/OL]. Journal of Third Military Medical University 1-7(2022) DOI: 10.16016/j.1000-5404.1.
Correlation between Akp2 and myocardial fibrosis post myocardial infarction
目的 探讨组织非特异性碱性磷酸酶(alkaline phosphatase,Akp2)与心肌梗死(myocardial infraction,MI)后心肌纤维化的关系。方法 收集2019年3—11月本院收治的46例急性心肌梗死患者为MI患者组,同期41例冠脉造影检查阴性患者为对照组,Akp2试剂盒测定血清Akp2活性,酶联免疫法测定血清Ⅰ型前胶原羧基端肽(procollagen type I C-peptide,PICP) 和Ⅲ型前胶原氨基端肽(procollagen III N-terminal peptide,PIIINP)的含量。收集5例陈旧性心肌梗死患者的心肌样本,天狼星红染色检测心脏纤维化水平,免疫组化方法检测Akp2表达情况。10只8周龄C57BL/6J雄性小鼠随机分为假手术组和心肌梗死组,每组5只,心梗术后2周取心脏标本,Masson染色检测其胶原面积,免疫组化方法检测Akp2表达情况。结果 与对照组比较,MI患者组血清Akp2活性[ (8.49±3.30)金氏单位/100 mL]显著增加(
To investigate the relationship between alkaline phosphatase (Akp2) and myocardial fibrosis post myocardial infarction(MI).
Methods
2
Forty-six patients with acute MI were enrolled as the study group and forty-one patients with negative findings in coronary angiograms during the same period were collected as the control group. The serum Akp2 activity was detected by alkaline phosphatase kit. The concentration of PICP and PIIINP were detected by enzyme-linked immunosorbent assay. Myocardial tissues were collected from five patients who died of myocardial infarction. Collagen fiber area of heart was detected by Sirius red staining and the expression of Akp2 was detected by immunohistochemistry. Ten 8-week-old male C57BL/6J mice were randomly divided into sham group and MI group with five mice in each group. Mice were sacrificed two weeks post MI,Collagen fiber area of heart was detected by Masson staining and the expression of Akp2 was detected by immunohistochemistry.
Results
2
Compared with the control group, the serum Akp2 activity was increased in patients with myocardial infarction (
P<0.01
), the concentration of serum PICP and PIIINP in patients with myocardial infarction increased significantly (
P<0.01, P<0.01
). Moreover, the serum Akp2 activity was significantly correlated with the concentration of serum PICP and PIIINP(r=0.38,
P<0.01
,r=0.40,
P<0.01
).There was more collagen deposition in the infarct border area of remote myocardial infarction than in the distal infarct (
P<0.01
)
.
The expression of Akp2 was increased in patients with myocardial infarction (
P<0.01
). Compared with the sham group, the expression of Akp2 and Collagen fiber area in MI group increased significantly (
P<0.01, P<0.01
). The expression of Akp2 was consistent with the distribution of fibroscar in MI group.
Conclusion
2
Akp2 is related to the pathophysiological process of myocardial fibrosis after myocardial infarction.
关键词
组织非特异性碱性磷酸酶心肌梗死Ⅰ型前胶原羧基端肽Ⅲ型前胶原氨基端肽
Keywords
Akp2myocardial infarctionprocollagen type I C-peptideprocollagen III N-terminal peptide
references
WRITING GROUP MEMBERS, MOZAFFARIAN D, BENJAMIN E J, et al. Heart disease and stroke statistics-2016 update: a report from the American heart association[J]. Circulation, 2016, 133(4): e38-e360. DOI:10.1161/CIR.0000000000000350http://dx.doi.org/10.1161/CIR.0000000000000350.
Li X, Zhu L, Wang B, et al. Drugs and Targets in Fibrosis[J]. Front Pharmacol, 2017, 8(11): 855. DOI: 10.3389/fphar.2017.00855http://dx.doi.org/10.3389/fphar.2017.00855.
RICHARDS A M. Circulating biomarkers of cardiac fibrosis: do we have any and what use are they?[J]. Circ Heart Fail, 2017, 10(3): e003936. DOI:10.1161/CIRCHEARTFAILURE.117.003936http://dx.doi.org/10.1161/CIRCHEARTFAILURE.117.003936.
LÓPEZ B, GONZÁLEZ A, RAVASSA S, et al. Circulating biomarkers of myocardial fibrosis[J]. J Am Coll Cardiol, 2015, 65(22): 2449-2456. DOI:10.1016/j.jacc.2015.04.026http://dx.doi.org/10.1016/j.jacc.2015.04.026.
SHARMA U, PAL D, PRASAD R. Alkaline phosphatase: an overview[J]. Indian J Clin Biochem, 2014, 29(3): 269-278. DOI:10.1007/s12291-013-0408-yhttp://dx.doi.org/10.1007/s12291-013-0408-y.
MILLÁN J L. The role of phosphatases in the initiation of skeletal mineralization[J]. Calcif Tissue Int, 2013, 93(4): 299-306. DOI:10.1007/s00223-012-9672-8http://dx.doi.org/10.1007/s00223-012-9672-8.
SHEEN C R, KUSS P, NARISAWA S, et al. Pathophysiological role of vascular smooth muscle alkaline phosphatase in medial artery calcification[J]. J Bone Miner Res, 2015, 30(5): 824-836. DOI:10.1002/jbmr.2420http://dx.doi.org/10.1002/jbmr.2420.
HERNÁNDEZ-MOSQUEIRA C, VELEZ-DELVALLE C, KURI-HARCUCH W. Tissue alkaline phosphatase is involved in lipid metabolism and gene expression and secretion of adipokines in adipocytes[J]. Biochim Biophys Acta, 2015, 1850(12): 2485-2496. DOI:10.1016/j.bbagen.2015.09.014http://dx.doi.org/10.1016/j.bbagen.2015.09.014.
ARUN P, OGUNTAYO S, ALBERT S V, et al. Acute decrease in alkaline phosphatase after brain injury: a potential mechanism for tauopathy[J]. Neurosci Lett, 2015, 609: 152-158. DOI:10.1016/j.neulet.2015.10.036http://dx.doi.org/10.1016/j.neulet.2015.10.036.
FAKHRY M, ROSZKOWSKA M, BRIOLAY A, et al. TNAP stimulates vascular smooth muscle cell trans-differentiation into chondrocytes through calcium deposition and BMP-2 activation: Possible implication in atherosclerotic plaque stability[J]. Biochim Biophys Acta Mol Basis Dis, 2017, 1863(3): 643-653. DOI:10.1016/j.bbadis.2016.12.003http://dx.doi.org/10.1016/j.bbadis.2016.12.003.
OH P C, LEE K, KIM T H, et al. Prognostic impact of alkaline phosphatase measured at time of presentation in patients undergoing primary percutaneous coronary intervention for ST-segment elevation myocardial infarction[J]. PLoS One, 2017, 12(2): e0171914. DOI:10.1371/journal.pone.0171914http://dx.doi.org/10.1371/journal.pone.0171914.
HAARHAUS M, BRANDENBURG V, KALANTAR-ZADEH K, et al. Alkaline phosphatase: a novel treatment target for cardiovascular disease in CKD[J]. Nat Rev Nephrol, 2017, 13(7): 429-442. DOI:10.1038/nrneph.2017.60http://dx.doi.org/10.1038/nrneph.2017.60.
UNSÖLD B, KAUL A, SBROGGIÒ M, et al. Melusin protects from cardiac rupture and improves functional remodelling after myocardial infarction[J]. Cardiovasc Res, 2014, 101(1): 97-107. DOI:10.1093/cvr/cvt235http://dx.doi.org/10.1093/cvr/cvt235.
CAO Y, WANG L L. Effects of vascular endothelial growth factor combined with basic fibroblast growth factor on periodontal ligament fibroblast proliferation and alkaline phosphatase activity in rats[J]. Chin J Tissue Eng Res, 2017, 21(4): 580-585. DOI:10.3969/j.issn.2095-4344.2017.04.015http://dx.doi.org/10.3969/j.issn.2095-4344.2017.04.015.[万方]
RODIONOV R N, BEGMATOV H, JARZEBSKA N, et al. Homoarginine supplementation prevents left ventricular dilatation and preserves systolic function in a model of coronary artery disease[J]. J Am Heart Assoc, 2019, 8(14): e012486. DOI:10.1161/JAHA.119.012486http://dx.doi.org/10.1161/JAHA.119.012486.
YU T T, JIAO Y D, SONG J, et al. Prognostic impact of alkaline phosphatase for in-hospital mortality in patients with acute coronary syndrome: a prospective cohort study in China[J]. BMJ Open, 2019, 9(8): e025648. DOI:10.1136/bmjopen-2018-025648http://dx.doi.org/10.1136/bmjopen-2018-025648.
GYÖNGYÖSI M, WINKLER J, RAMOS I, et al. Myocardial fibrosis: biomedical research from bench to bedside[J]. Eur J Heart Fail, 2017, 19(2): 177-191. DOI:10.1002/ejhf.696http://dx.doi.org/10.1002/ejhf.696.
BHATT A S, AMBROSY A P, VELAZQUEZ E J. Adverse remodeling and reverse remodeling after myocardial infarction[J]. Curr Cardiol Rep, 2017, 19(8): 71. DOI:10.1007/s11886-017-0876-4http://dx.doi.org/10.1007/s11886-017-0876-4.
WANG F F, CHEN B X, YU H Y, et al. Correlation between growth differentiation factor-15 and collagen metabolism indicators in patients with myocardial infarction and heart failure[J]. J Geriatr Cardiol, 2016, 13(1): 88-93. DOI:10.11909/j.issn.1671-5411.2016.01.002http://dx.doi.org/10.11909/j.issn.1671-5411.2016.01.002.
RADOVAN J, VACLAV P, PETR W, et al. Changes of collagen metabolism predict the left ventricular remodeling after myocardial infarction[J]. Mol Cell Biochem, 2006, 293(1/2): 71-78. DOI:10.1007/s11010-006-2955-5http://dx.doi.org/10.1007/s11010-006-2955-5.
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