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2
A multiplexed immunocapture liquid chromatography tandem mass spectrometry assay for the simultaneous measurement of myostatin and GDF-11 in rat serum using an automated sample preparation platform.一种使用自动化样本制备平台同时测量大鼠血清中肌肉生长抑制素和 GDF-11 的多重免疫捕获液相色谱串联质谱检测法。
Anal Chim Acta. 2017 Aug 1;979:36-44. doi: 10.1016/j.aca.2017.04.028. Epub 2017 Apr 26.
3
Supraphysiological levels of GDF11 induce striated muscle atrophy.
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EMBO Mol Med. 2017 Apr;9(4):531-544. doi: 10.15252/emmm.201607231.
4
Structural basis for potency differences between GDF8 and GDF11.生长分化因子8(GDF8)和生长分化因子11(GDF11)效力差异的结构基础。
BMC Biol. 2017 Mar 3;15(1):19. doi: 10.1186/s12915-017-0350-1.
5
Targeted myocardial delivery of GDF11 gene rejuvenates the aged mouse heart and enhances myocardial regeneration after ischemia-reperfusion injury.GDF11基因靶向心肌递送可使衰老小鼠心脏恢复活力,并增强缺血再灌注损伤后的心肌再生能力。
Basic Res Cardiol. 2017 Jan;112(1):7. doi: 10.1007/s00395-016-0593-y. Epub 2016 Dec 21.
6
Serum myostatin levels are independently associated with skeletal muscle wasting in patients with heart failure.血清肌抑素水平与心力衰竭患者的骨骼肌萎缩独立相关。
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7
Quantification of GDF11 and Myostatin in Human Aging and Cardiovascular Disease.人类衰老和心血管疾病中生长分化因子11(GDF11)和肌肉生长抑制素的定量分析。
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8
Biochemistry and Biology of GDF11 and Myostatin: Similarities, Differences, and Questions for Future Investigation.生长分化因子11和肌肉生长抑制素的生物化学与生物学:异同点及未来研究问题
Circ Res. 2016 Apr 1;118(7):1125-41; discussion 1142. doi: 10.1161/CIRCRESAHA.116.308391.
9
Questions and Answers About Myostatin, GDF11, and the Aging Heart.关于肌肉生长抑制素、生长分化因子11与衰老心脏的问答
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10
Hypertrophic cardiomyopathy in man and cats.人类和猫的肥厚型心肌病。
J Vet Cardiol. 2015 Dec;17 Suppl 1:S6-9. doi: 10.1016/j.jvc.2015.03.007.

肥厚型心肌病继发充血性心力衰竭猫的血浆生长分化因子8和11水平

Plasma growth differentiation factors 8 and 11 levels in cats with congestive heart failure secondary to hypertrophic cardiomyopathy.

作者信息

Yang V K, Rush J E, Bhasin S, Wagers A J, Lee R T

机构信息

Department of Clinical Sciences, Cummings School of Veterinary Medicine at Tufts University, 200 Westboro Rd, North Grafton, MA, 01536, USA.

Department of Clinical Sciences, Cummings School of Veterinary Medicine at Tufts University, 200 Westboro Rd, North Grafton, MA, 01536, USA.

出版信息

J Vet Cardiol. 2019 Oct;25:41-51. doi: 10.1016/j.jvc.2019.08.002. Epub 2019 Sep 1.

DOI:10.1016/j.jvc.2019.08.002
PMID:31568985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7703810/
Abstract

OBJECTIVES

Growth differentiation factor (GDF) 11 has been shown to reduce cardiac hypertrophy in mice. Low levels of GDF-11 are associated with cardiac hypertrophy in humans. The authors hypothesized that plasma GDF-11 level is decreased in cats with hypertrophic cardiomyopathy (HCM). Given the close homology between GDF-11 and myostatin/GDF-8, GDF-8 levels were also assessed.

ANIMALS

Thirty-seven client-owned cats were enrolled, including cats with normal cardiac structure (n = 16), cats with HCM or hypertrophic obstructive cardiomyopathy (HOCM; n = 14), and cats with HCM and congestive heart failure (CHF; n = 7).

METHODS

Plasma samples were analyzed for GDF-8 and GDF-11 using liquid chromatography tandem-mass spectrometry. Levels of GDF-8 and GDF-11 were compared between cats with normal cardiac structure, HCM or HOCM, and CHF.

RESULTS

No differences in GDF-11 concentrations were found between cats with normal cardiac structure and cats with HCM/HOCM, with or without history of CHF. Decreased GDF-8 concentrations were detected in cats with CHF compared to cats with HCM/HOCM without history of CHF (p=0.031) and cats with normal cardiac structure (p=0.027). Growth differentiation factor 8 was higher in cats with HOCM compared to those with CHF (p=0.002). No statistical difference was noted in GDF-8 level as a function of age, weight, or body condition score.

CONCLUSIONS

Plasma GDF-11 was not different between cats with HCM/HOCM and cats with normal cardiac structure regardless of age. Plasma GDF-8 was decreased in cats with CHF compared to cats with normal cardiac structure and cats with asymptomatic HCM/HOCM, suggesting a possible role in CHF development.

摘要

目的

生长分化因子(GDF)11已被证明可减轻小鼠的心脏肥大。人类中GDF-11水平较低与心脏肥大有关。作者推测肥厚型心肌病(HCM)猫的血浆GDF-11水平会降低。鉴于GDF-11与肌肉生长抑制素/GDF-8之间的密切同源性,还评估了GDF-8水平。

动物

纳入37只客户拥有的猫,包括心脏结构正常的猫(n = 16)、患有HCM或肥厚性梗阻性心肌病(HOCM;n = 14)的猫以及患有HCM和充血性心力衰竭(CHF;n = 7)的猫。

方法

使用液相色谱串联质谱法分析血浆样本中的GDF-8和GDF-11。比较心脏结构正常的猫、患有HCM或HOCM的猫以及患有CHF的猫之间GDF-8和GDF-11的水平。

结果

心脏结构正常的猫与患有HCM/HOCM的猫(无论有无CHF病史)之间,GDF-11浓度没有差异。与无CHF病史的HCM/HOCM猫(p = 0.031)和心脏结构正常的猫(p = 0.027)相比,CHF猫的GDF-8浓度降低。与CHF猫相比,HOCM猫的生长分化因子8更高(p = 0.002)。未发现GDF-8水平随年龄、体重或身体状况评分有统计学差异。

结论

无论年龄如何,HCM/HOCM猫与心脏结构正常的猫之间血浆GDF-11没有差异。与心脏结构正常的猫和无症状HCM/HOCM猫相比,CHF猫的血浆GDF-8降低,提示其在CHF发展中可能起作用。