Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits

Objective To investigate whether ischemic preconditioning (IP) attenuates endothelial injury induced by arterial puncture. Methods Rabbits were divided into control group, ischemic preconditioning group (IP group), femoral artery puncture group (P group) and ischemic preconditioning+femoral artery...

Full description

Bibliographic Details
Main Author: LIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao
Format: Article
Language:zho
Published: Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2022-12-01
Series:Jichu yixue yu linchuang
Subjects:
Online Access:http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-12-1817.pdf
_version_ 1797365872135766016
author LIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao
author_facet LIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao
author_sort LIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao
collection DOAJ
description Objective To investigate whether ischemic preconditioning (IP) attenuates endothelial injury induced by arterial puncture. Methods Rabbits were divided into control group, ischemic preconditioning group (IP group), femoral artery puncture group (P group) and ischemic preconditioning+femoral artery puncture group (IP-P group). The expression of PI3K, AKT and eNOS in endothelial tissue was determined by immuno-histochemistry. p-AKT and p-eNOS were detected by Western blot. eNOS was detected by RT-qPCR. Plasma NO was detected by enzyme-linked immunosorbent assay(ELISA). Results The expression of PI3K, AKT and eNOS in the vascular endothelium of IP-P group was higher than that from P group and lower than that from IP group(P<0.05). The expression of p-AKT and p-eNOS in IP-P group was higher than that from P group(P<0.05). The expression of eNOS in IP-P group was higher than that from P group and lower than that from IP group(P<0.05). Plasma NO level in IP-P group was higher than that in P group and lower than that in IP group (P<0.05). Conclusions IP promotes eNOS phos-phorylation and NO synthesis in rabbit vascular endothelium, which may be one of the potential mechanisms by which IP reduces endothelial injury before arterial puncture.
first_indexed 2024-03-08T16:55:08Z
format Article
id doaj.art-9e306f7200be4d9f9c6a2b35d829527a
institution Directory Open Access Journal
issn 1001-6325
language zho
last_indexed 2024-03-08T16:55:08Z
publishDate 2022-12-01
publisher Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.
record_format Article
series Jichu yixue yu linchuang
spelling doaj.art-9e306f7200be4d9f9c6a2b35d829527a2024-01-05T02:36:47ZzhoInstitute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.Jichu yixue yu linchuang1001-63252022-12-0142121817182210.16352/j.issn.1001-6325.2022.12.1817Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbitsLIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao01. Department of Cardiovascular Medicine, Affiliated Central Hospital of Shandong First Medical University, Jinan 250000; ;2. Shandong Clinical Center of Public Health, Jinan 250000, ChinaObjective To investigate whether ischemic preconditioning (IP) attenuates endothelial injury induced by arterial puncture. Methods Rabbits were divided into control group, ischemic preconditioning group (IP group), femoral artery puncture group (P group) and ischemic preconditioning+femoral artery puncture group (IP-P group). The expression of PI3K, AKT and eNOS in endothelial tissue was determined by immuno-histochemistry. p-AKT and p-eNOS were detected by Western blot. eNOS was detected by RT-qPCR. Plasma NO was detected by enzyme-linked immunosorbent assay(ELISA). Results The expression of PI3K, AKT and eNOS in the vascular endothelium of IP-P group was higher than that from P group and lower than that from IP group(P<0.05). The expression of p-AKT and p-eNOS in IP-P group was higher than that from P group(P<0.05). The expression of eNOS in IP-P group was higher than that from P group and lower than that from IP group(P<0.05). Plasma NO level in IP-P group was higher than that in P group and lower than that in IP group (P<0.05). Conclusions IP promotes eNOS phos-phorylation and NO synthesis in rabbit vascular endothelium, which may be one of the potential mechanisms by which IP reduces endothelial injury before arterial puncture.http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-12-1817.pdfischemic preconditioning|femoral artery puncture|pi3k/akt|enos
spellingShingle LIU Peng, LI Kai-yuan, YANG Yang, MAN Yi-long, DU Feng-li, LIU Miao
Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
Jichu yixue yu linchuang
ischemic preconditioning|femoral artery puncture|pi3k/akt|enos
title Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
title_full Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
title_fullStr Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
title_full_unstemmed Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
title_short Ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
title_sort ischemic preconditioning attenuates endothelial injury induced by femoral artery puncture in rabbits
topic ischemic preconditioning|femoral artery puncture|pi3k/akt|enos
url http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/1001-6325-2022-42-12-1817.pdf
work_keys_str_mv AT liupenglikaiyuanyangyangmanyilongdufengliliumiao ischemicpreconditioningattenuatesendothelialinjuryinducedbyfemoralarterypunctureinrabbits