A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction.
A novel soluble epoxide hydrolase vaccine protects murine cardiac muscle against myocardial infarction.
复制标题
一种新型的可溶性环氧化物水解酶疫苗可保护鼠心肌免受心肌梗塞。
DOI:
10.1038/s41598-022-10641-x
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发表时间:
2022-04-28
影响因子:
4.6
通讯作者:
Node, Koichi
中科院分区:
文献类型:
--
作者:
Kitsuka, Takahiro;Shiraki, Aya;Oyama, Jun-ichi;Nakagami, Hironori;Tanaka, Atsushi;Node, Koichi
Myocardial infarction is still a life-threatening disease, even though its prognosis has been improved through the development of percutaneous coronary intervention and pharmacotherapy. In addition, heart failure due to remodeling after myocardial infarction requires lifelong management. The aim of this study was to develop a novel treatment suppressing the myocardial damage done by myocardial infarction. We focused on inhibition of soluble epoxide hydrolase to prolong the activation of epoxyeicosatrienoic acids, which have vasodilatory and anti-inflammatory properties. We successfully made a new vaccine to inactivate soluble epoxide hydrolase, and we have evaluated the effect of the vaccine in a rat myocardial infarction model. In the vaccinated group, the ischemic area was significantly reduced, and cardiac function was significantly preserved. Vaccine treatment clearly increased microvessels in the border area and suppressed fibrosis secondary to myocardial infarction. This soluble epoxide hydrolase vaccine is a novel treatment for improving cardiac function following myocardial infarction.
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DOI:
10.1136/heartjnl-2016-309983
发表时间:
2016-12-15
期刊:
Heart (British Cardiac Society)
影响因子:
--
作者:
MacIntyre CR;Mahimbo A;Moa AM;Barnes M
通讯作者:
Barnes M
影响因子:
168.9
作者:
Lozano, Rafael;Naghavi, Mohsen;Murray, Christopher J. L.
通讯作者:
Murray, Christopher J. L.
DOI:
10.1152/ajpheart.00186.2008
发表时间:
2008-06-01
影响因子:
4.8
作者:
Gross, Garrett J.;Gauthier, Kathryn M.;Nithipatikom, Kasem
通讯作者:
Nithipatikom, Kasem
影响因子:
3.7
作者:
COOPER, CJ;PFEFFER, JM;PFEFFER, MA
通讯作者:
PFEFFER, MA
影响因子:
5.3
作者:
Guo Y;Luo F;Zhang X;Chen J;Shen L;Zhu Y;Xu D
通讯作者:
Xu D