Proarrhythmic risk and determinants of cardiac autonomic dysfunction in collagen-induced arthritis rats.
Proarrhythmic risk and determinants of cardiac autonomic dysfunction in collagen-induced arthritis rats.
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胶原诱导的关节炎大鼠的致心律失常风险和心脏自主神经功能障碍的决定因素
DOI:
10.1186/s12891-016-1347-6
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发表时间:
2016-11-29
影响因子:
2.3
通讯作者:
Lin SF
中科院分区:
文献类型:
--
作者:
Lin TT;Sung YL;Wu CE;Zhang H;Liu YB;Lin SF
Patients with rheumatoid arthritis (RA) have increased risk of sudden cardiac death (SCD), which is two-fold higher than general population. The driving cause of SCD was considered due to lift-threatening arrhythmia where systemic inflammation acts as the pathophysiological basis linking RA to autonomicdysfunction. To assess the sympathetic over-activity of “inflammatory reflex”, we measured heart rate variability (HRV) in a rat collagen-induced arthritis (CIA) model, whose arthritis is induced in Lewis rats by intradermal injection of emulsion of type II collagen. Single-lead electrocardiogram (ECG) was recorded for 30 min every two days. Time and frequency-domain parameters, detrended fluctuation analysis (DFA), deceleration (DC) and acceleration capacity (AC) were analyzed. Compared with 9 control rats, many of HRV parameters of 9 CIA rats revealed significant different. At the beginning of arthritis, LF/HF was significant higher than controls (1st week: 2.41 ± 0.7 vs. 1.76 ± 0.6, p < 0.05; 2nd week: 2.24 ± 0.5 vs. 1.58 ± 0.5, p < 0.05) indicating intensive inflammatory reflex at the initial phase of inflammation but no significant difference was observed in the following recover phase. The similar trend of DFA parameters was noted. However, the DC appeared progressive lower despite of no significant increase of the LF/HF compared with controls since 4th week. We observed sympathetic over-activation of inflammatory reflex during early stage of arthritis in CIA rats. The ongoing decline of DC indicated advanced cardiac autonomic dysfunction regardless of remission of acute arthritis. The online version of this article (doi:10.1186/s12891-016-1347-6) contains supplementary material, which is available to authorized users.
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影响因子:
13.6
作者:
Stojanovich, Ljudmila
通讯作者:
Stojanovich, Ljudmila
DOI:
10.1007/978-1-60761-058-8_11
发表时间:
2010-01-01
期刊:
MOUSE MODELS FOR DRUG DISCOVERY: METHODS AND PROTOCOLS
影响因子:
--
作者:
Bevaart, Lisette;Vervoordeldonk, Margriet J.;Tak, Paul P.
通讯作者:
Tak, Paul P.
影响因子:
168.9
作者:
Bauer, Axel;Kantelhardt, Jan W.;Schmidt, Georg
通讯作者:
Schmidt, Georg
影响因子:
2.6
作者:
Aydemir, M.;Yazisiz, V.;Terzioglu, E.
通讯作者:
Terzioglu, E.
影响因子:
10.8
作者:
LI, YH;ROZANSKI, GJ
通讯作者:
ROZANSKI, GJ