Abstract

The infarct size-limiting effect elicited by cold acclimation (CA) is accompanied by increased mitochondrial resistance and unaltered β1-adrenergic receptor (AR) signaling persisting for 2 wk at room temperature. As the mechanism of CA-elicited cardioprotection is not fully understood, we examined the role of the salvage β2-AR/Gi/Akt pathway. Male Wistar rats were exposed to CA (8°C, 5 wk), whereas the recovery group (CAR) was kept at 24°C for additional 2 wk. We show that the total number of myocardial β-ARs in the left ventricular myocardium did not change after CA but decreased after CAR. We confirmed the infarct size-limiting effect in both CA and CAR groups. Acute administration of β2-AR inhibitor ICI-118551 abolished the protective effect in the CAR group but had no effect in the control and CA groups. The inhibitory Giα1/2 and Giα3 proteins increased in the membrane fraction of the CAR group, and the phospho-Akt (Ser473)-to-Akt ratio also increased. Expression, phosphorylation, and mitochondrial location of the Akt target glycogen synthase kinase (GSK-3β) were affected neither by CA nor by CAR. However, GSK-3β translocated from the Z-disk to the H-zone after CA, and acquired its original location after CAR. Our data indicate that the cardioprotection observed after CAR is mediated by the β2-AR/Gi pathway and Akt activation. Further studies are needed to unravel downstream targets of the central regulators of the CA process and the downstream targets of the Akt protein after CAR.NEW & NOTEWORTHY Cardioprotective effect of cold acclimation and that persisting for 2 wk after recovery engage in different mechanisms. The β2-adrenoceptor/Gi pathway and Akt are involved only in the mechanism of infarct size-limiting effect occurring during the recovery phase. GSK-3β translocated from the Z-line to the H-zone of sarcomeres by cold acclimation returns back to the original position after the recovery phase. The results provide new insights potentially useful for the development of cardiac therapies.

Highlights

  • Despite intensive research, acute myocardial infarction remains a leading cause of death and disability

  • Proper acclimation to low temperature was confirmed by significantly increased weight of brown adipose tissue (BAT) after cold acclimation (CA)

  • A competitive receptor-binding assay demonstrated increased proportion of b2-adrenergic receptor (AR) within total b-AR in crude myocardial membrane fraction after CAR but not after CA. This effect was confirmed by acute administration of the specific b2-AR inhibitor ICI-118551, which abolished the infarct size-lowering effect persisting after CAR, but not that elicited by CA

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Summary

Introduction

Acute myocardial infarction remains a leading cause of death and disability. It was reported that cold acclimation (CA) possesses an infarct size-limiting effect [1, 2]. We have documented that exposure of rats to 5 wk of gradual mild cold acclimation (CA), followed by 2 wk of recovery resulted in reduction of myocardial infarct size without apparent side effects such as hypertension or hypertrophy. Our recent study showed that cold-induced cardioprotection implies an unaltered b1-AR/adenylyl cyclase/cAMP pathway, including stable levels of phosphorylated PKA and Gs. We confirmed the finding by acute administration of b1-AR antagonist (metoprolol), which did not affect the CA-elicited cardioprotection. Increased b2-AR translocation to the COLD ACCLIMATION PERSISTING CARDIOPROTECTION BY b2-AR/Gi/Akt membrane fraction was observed after CA, and it remained upregulated for 2 wk of recovery at 24C following CA [1]

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