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1 followed by 15 min of reflow before harvest (ischemic preconditioning).
2 r, could suffice to mediate local and remote ischemic preconditioning.
3 tion and showed no protection in response to ischemic preconditioning.
4 PKMzeta levels were elevated 3 days after ischemic preconditioning.
5 cate key roles of PKMzeta and Na/K ATPase in ischemic preconditioning.
6 compounds blocked neuroprotection following ischemic preconditioning.
7 tion comparable to wild-type mice exposed to ischemic preconditioning.
8 lation of Src and Cav-1 after isoflurane and ischemic preconditioning.
9 idative injury and abolish the late phase of ischemic preconditioning.
10 infarction by a mechanism similar to that of ischemic preconditioning.
11 e hypothesis that cardiac nerves may mediate ischemic preconditioning.
12 onged ischemic insult, a phenomenon known as ischemic preconditioning.
13 arct size observed in WT after a protocol of ischemic preconditioning.
14 protective effect that normally occurs after ischemic preconditioning.
15 by very short periods of ischemia, so-called ischemic preconditioning.
16 7 is upregulated in the retina after retinal ischemic preconditioning.
17 to learning and memory, drug tolerance, and ischemic preconditioning.
18 ntributes to the early protective effects of ischemic preconditioning.
19 rdiac myocytes during ischemia is delayed by ischemic preconditioning.
20 teatosis were also particularly protected by ischemic preconditioning.
21 lethal ischemic insult, in a process termed ischemic preconditioning.
22 factors affecting the protective effects of ischemic preconditioning.
23 spase cleavage of PARP-1 could contribute to ischemic preconditioning.
24 the kidney protection afforded by 30 min of ischemic preconditioning.
25 ion injury, and epsilon-PKC activator mimics ischemic preconditioning.
26 naling pathway may play an important role in ischemic preconditioning.
27 ficantly reduced in mice treated with remote ischemic preconditioning.
28 role in protecting the heart from injury in ischemic preconditioning.
29 se channels as key players in the process of ischemic preconditioning.
30 as triggers and end effectors in myocardial ischemic preconditioning.
31 sinusoidal endothelial cell protection after ischemic preconditioning.
32 receptor blockade did not prevent protective ischemic preconditioning.
33 may be the final mediator of protection for ischemic preconditioning.
34 No adverse events were reported with remote ischemic preconditioning.
35 y component of signaling cascades leading to ischemic preconditioning.
36 nd reperfusion, a phenomenon known as remote ischemic preconditioning.
37 -reperfusion injury, and cardioprotection by ischemic preconditioning.
38 ene transcription and is required for remote ischemic preconditioning.
39 rts where the expected loss was prevented by ischemic preconditioning.
40 nd loss of the cardioprotection conferred by ischemic preconditioning.
41 major adverse events were related to remote ischemic preconditioning.
42 f metalloproteinases 2 after surgery (remote ischemic preconditioning, 0.36 vs control, 0.97 ng/mL2/1
43 nts [27.7%], respectively; hazard ratio with ischemic preconditioning, 0.95; 95% confidence interval,
45 tion comparable to that of the late phase of ischemic preconditioning (29+/-3%, P<0.01 group II versu
47 injury was significantly reduced with remote ischemic preconditioning (45 of 120 patients [37.5%]) co
48 R-21 in the infarcted areas was inhibited by ischemic preconditioning, a known cardiac protective met
49 channels in the heart is believed to mediate ischemic preconditioning, a phenomenon whereby brief per
52 whether the cardioprotective intervention of ischemic preconditioning affected mitochondrial protein
58 erved for comparisons involving xanthine and ischemic preconditioning, although the impact of NAC and
59 jury (IRI) and may signal the development of ischemic preconditioning, an adaptive state that is prot
60 ilon gene blocked cardioprotection caused by ischemic preconditioning and alpha(1)-adrenergic recepto
61 out the role of bone marrow-derived cells in ischemic preconditioning and also reveal that distinct m
62 tivate signaling pathways that contribute to ischemic preconditioning and cardioprotection, high leve
63 e to hypoxic stress with involvement in both ischemic preconditioning and delayed neuroprotection.
66 s have been reported to mediate both cardiac ischemic preconditioning and ischemia/reperfusion injury
67 erase-5 inhibitors and beneficial actions of ischemic preconditioning and ischemic postconditioning b
68 heart against ischemia-reperfusion injury by ischemic preconditioning and K(ATP) channel openers is k
70 over, ethanol abolished protection from both ischemic preconditioning and mitochondrial KATP channel
72 l ischemia of internal organs induces local (ischemic preconditioning) and systemic (RIPC) resistance
74 ts of ischemic preconditioning (IPC), remote ischemic preconditioning, and ischemic postconditioning
76 Although xanthine, NAC, NaHCO3, NAC+NaHCO3, ischemic preconditioning, and natriuretic peptide may ha
78 n of the cGMP-degrading phosphodiesterase-5, ischemic preconditioning, and postconditioning regimens.
79 c mitoK(ATP) channels play a pivotal role in ischemic preconditioning, and thus represent interesting
81 to evaluate the clinical evidence for remote ischemic preconditioning as a potential strategy to prot
85 that is at least as powerful as traditional ischemic preconditioning but is mediated through radical
87 an important role in cardiac development and ischemic preconditioning, but the mechanism underlying t
88 an obligatory mediator of the late phase of ischemic preconditioning, but the mechanisms of its card
89 reconcile the controversy over the basis of ischemic preconditioning by demonstrating that SDH is a
90 ain how mitoK(ATP) channel activation mimics ischemic preconditioning by protecting mitochondria as t
93 patients undergoing cardiac surgery, remote ischemic preconditioning compared with no ischemic preco
95 fter induction of anesthesia) or sham remote ischemic preconditioning (control), both via blood press
97 to the temporally distinct acute and delayed ischemic preconditioning cytoprotective phenotypes, we r
99 e hypothesized that RIC before shock (remote ischemic preconditioning), during shock (remote ischemic
100 ic transgenic activation of PKCepsilon or by ischemic preconditioning enhances the formation of PKCep
101 e propose that, at 48 h of reperfusion after ischemic preconditioning, epsilonPKC is poised at synapt
102 cted to sublethal transient global ischemia (ischemic preconditioning) exhibit neuroprotection agains
104 n, patients were randomly assigned to remote ischemic preconditioning (four 5-minute inflations and d
105 rate at 6 years remained lower in the remote ischemic preconditioning group (hazard ratio, 0.58; 95%
106 the control group and 6 (12%) in the remote ischemic preconditioning group (odds ratio, 0.21; 95% co
107 12 months between the patients in the remote ischemic preconditioning group and those in the control
108 is early benefit in MACCE rate in the remote ischemic preconditioning group was sustained long-term.
109 parable in the intermittent clamping and the ischemic preconditioning group, whereas intermittent cla
110 nts (811 in the control group and 801 in the ischemic-preconditioning group) at 30 cardiac surgery ce
112 synthase kinase (GSK) inhibition produced by ischemic preconditioning has been previously shown to be
118 c postconditioning and all studies on remote ischemic preconditioning in patients with AMI reported r
123 ve shown tissue-protective effects of remote ischemic preconditioning in various target organs, inclu
124 ethanol exposure has been reported to mimic ischemic preconditioning in vitro, but it failed to prot
126 e of the species-related differences seen in ischemic preconditioning in which one redundant pathway
127 ATP content in liver tissue was preserved by ischemic preconditioning in young but not older patients
128 te analysis revealed an increased benefit of ischemic preconditioning in younger patients, in patient
129 In this study, we demonstrate that remote ischemic preconditioning increases plasma IL-10 levels a
131 -10) levels play an important role in remote ischemic preconditioning induced by clamping the femoral
132 ippocampal neurons, the protective effect of ischemic preconditioning induced by oxygen-glucose depri
133 genomic profile of cardioprotection between ischemic preconditioning induced by RCS and that induced
134 ar mechanisms differ markedly when mediating ischemic preconditioning induced by repetitive episodes
138 hort- and long-term clinical consequences of ischemic preconditioning (IP) during percutaneous corona
145 ib) abolishes the cardioprotective effect of ischemic preconditioning (IP), presumably by inhibiting
147 /L) abolished the protection associated with ischemic preconditioning (IPC) (20.2+/-3.6% versus 45.9+
150 silon activation is necessary for myocardial ischemic preconditioning (IPC) and PKC activators increa
151 ecently, it was demonstrated that both renal ischemic preconditioning (IPC) and systemic adenosine pr
152 vascular bundle was compared against direct ischemic preconditioning (IPC) and the standard of care
153 disease, this study compares the effects of ischemic preconditioning (IPC) and therapies targeting v
159 2-LO) has been shown to be a factor in acute ischemic preconditioning (IPC) in the isolated rat heart
166 ma-based AAR (% of left ventricle) following ischemic preconditioning (IPC) or cyclosporin-A (CsA) tr
170 ction against cerebral ischemia conferred by ischemic preconditioning (IPC) requires translocation of
172 This study assessed the ability of remote ischemic preconditioning (IPC) to attenuate cardiac trop
173 up of isolated rabbit hearts were exposed to ischemic preconditioning (IPC) via 2 episodes of flow in
176 27 is specifically upregulated after retinal ischemic preconditioning (IPC), and this upregulation ac
177 K(ATP)) is implicated in cardioprotection by ischemic preconditioning (IPC), but the molecular identi
179 schemic injury in a natural process known as ischemic preconditioning (IPC), induced a rapid release
180 l infarct size and the protective effects of ischemic preconditioning (IPC), remote ischemic precondi
181 obal ischemia and the tolerance conferred by ischemic preconditioning (IPC), would reveal new neuropr
188 nomenon whereby a sublethal ischemic insult [ischemic preconditioning (IPC)] provides robust protecti
189 5+/-4.1% (P<0.01), an effect comparable with ischemic preconditioning (IPC; 27.5+/-2.3%; P<0.01).
190 e short episodes of forearm ischemia (remote ischemic preconditioning [IPC]) reduce exercise-induced
196 Understanding the mechanisms responsible for ischemic preconditioning is important for formulating th
197 sp70.3 gene in the myocardium in response to ischemic preconditioning is NF-kappaB-dependent and nece
201 t, which abrogates the protective effects of ischemic preconditioning, is not associated with ischemi
202 is area, the appropriate intensity of remote ischemic preconditioning, its mechanisms of action, and
203 infarct-sparing effect of the late phase of ischemic preconditioning (late PC) lasts for 72 hours.
208 atio to standard care with (n=50) or without ischemic preconditioning (n=50; intermittent arm ischemi
209 ice was similar to wild-type mice undergoing ischemic preconditioning; no increased protection was ob
213 e secondary to recruitment of collaterals or ischemic preconditioning of the myocardium, and they app
216 led trial was to assess the impact of remote ischemic preconditioning on contrast medium-induced acut
217 There was no significant effect of remote ischemic preconditioning on myocardial infarction, strok
223 of coronary occlusion/reperfusion preceding (ischemic preconditioning) or following (ischemic postcon
224 short period of ischemia before transection (ischemic preconditioning), or pharmacological preconditi
226 ic acid (aspirin) (ASA) on the late phase of ischemic preconditioning (PC) against myocardial stunnin
227 endothelial nitric oxide synthase (eNOS) in ischemic preconditioning (PC) and cardioprotection is po
228 ecent studies suggest that the late phase of ischemic preconditioning (PC) can be mimicked by pretrea
229 ardioprotective effects of the late phase of ischemic preconditioning (PC) can be mimicked pharmacolo
231 ed the hypothesis that cardioprotection with ischemic preconditioning (PC) is lost in the aging, or s
232 To investigate its role in the late phase of ischemic preconditioning (PC), conscious rabbits underwe
233 rigger and the mediator of the late phase of ischemic preconditioning (PC), it is unknown whether NO
238 ardioprotective effects of the late phase of ischemic preconditioning (PC); however, the signaling pa
239 neurons overexpressing NCX1 and subjected to ischemic preconditioning (PC+OGD/RX), the neurotoxic eff
245 surgery to either receive or not receive an ischemic preconditioning protocol (10 minutes of ischemi
247 ; 95% CI, 2.25%-17.75%; P = .01), and remote ischemic preconditioning reduced intensive care unit sta
248 (CRISP Stent) study demonstrated that remote ischemic preconditioning reduced procedural symptoms, EC
258 y assess the renoprotective effect of remote ischemic preconditioning (RIPC) in patients undergoing a
262 time course and neuronal mechanism of remote ischemic preconditioning (RIPC) of the vasculature in hu
264 f this study was to determine whether remote ischemic preconditioning (RIPC) protects aged liver agai
268 duction of myocardial infarct size by remote ischemic preconditioning (RIPC), that is, cycles of isch
274 r results between centers and confirmed that ischemic preconditioning significantly reduced infarct s
275 te ischemic preconditioning compared with no ischemic preconditioning significantly reduced the rate
276 ked the protection afforded by both NMDA and ischemic preconditioning significantly, suggesting a sig
278 ium channel function plays a central role in ischemic preconditioning, stunned myocardium, and in ane
280 on angina may act as a clinical surrogate of ischemic preconditioning that may reduce infarct size an
281 on was markedly reduced in a model of kidney ischemic preconditioning that was established in the mou
283 enation-dependent Nrf-2 activity facilitates ischemic preconditioning through the induction of antiox
285 To validate CAESAR, we tested the ability of ischemic preconditioning to reduce infarct size in 3 spe
292 een caspase activation, PARP-1 cleavage, and ischemic preconditioning was supported by studies using
293 naling molecules and have been implicated in ischemic preconditioning, we examined diazoxide-induced
296 tors of JNK and p38, was markedly reduced by ischemic preconditioning, whereas the post-ischemic phos
298 long term protection afforded the kidney by ischemic preconditioning, which results in persistent re
300 sham laparotomy (n = 10, 2) I/R (n = 25), 3) ischemic preconditioning with 5 min of ischemia and 10 m
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