Buffer glucose adjustment affects myocardial function after ischemia-reperfusion in long-term diabetic rat isolated hearts.


Journal

Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800

Informations de publication

Date de publication:
11 2022
Historique:
revised: 22 06 2022
received: 27 03 2022
accepted: 24 06 2022
entrez: 3 11 2022
pubmed: 4 11 2022
medline: 5 11 2022
Statut: ppublish

Résumé

Due to its comorbidities type 2 diabetes mellitus (T2DM) and hypertension, the Zucker Spontaneous Hypertensive Fatty (ZSF1) rat is a clinically relevant animal model when assessing ischemia-reperfusion (IR) injury. Most IR studies in hearts isolated from diabetic animals have been conducted at normal glucose concentrations, providing a different environment compared to in-vivo. We hypothesized IR injury to be attenuated in isolated hearts of diabetic ZSF1 rats when adjusting the Krebs-buffer (KB) to their in-vivo, i.e., elevated blood glucose (BG) levels. Diabetic and non-diabetic ZSF1 rats were anesthetized, hearts isolated and Langendorff-prepared. While standard KB was used for the non-diabetic and diabetic unadjusted groups, KB with glucose levels increased to each rat's prior BG level was used for the adjusted diabetic group. All hearts underwent 30 min ischemia and 120 min reperfusion. Diastolic contracture during ischemia and early reperfusion was delayed and temporarily attenuated in the adjusted compared to the unadjusted diabetic and the non-diabetic groups. The decrease in coronary flow on reperfusion was attenuated in diabetic animals. Left ventricular developed pressure and contractility were not different among the three groups. Infarct size was significantly lower in non-diabetic animals; buffer adjustment made no difference in diabetic animals. In our study, T2DM did not worsen myocardial function in ZSF1 rat isolated hearts. Since our results reveal that hearts with an adjusted glucose level exhibit an at least temporary improvement of function following IR, further studies should consider adapting glucose levels to create more realistic conditions in isolated, perfused hearts.

Identifiants

pubmed: 36324287
doi: 10.14814/phy2.15387
pmc: PMC9630758
doi:

Substances chimiques

Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15387

Subventions

Organisme : BLRD VA
ID : I01 BX003482
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL123227
Pays : United States
Organisme : NIH HHS
ID : 5R01 HL123227
Pays : United States

Informations de copyright

© 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Claudius Balzer (C)

Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Anesthesiology, University Medicine Greifswald, Greifswald, Germany.

William J Cleveland (WJ)

Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Zhu Li (Z)

Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Matthias L Riess (ML)

Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Anesthesiology, TVHS VA Medical Center, Nashville, Tennessee, USA.
Department of Pharmacology, Vanderbilt University, Nashville, Tennessee, USA.

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