Research Article
Effects of Cardiac Hypertrophy, Diabetes, Aging, and
Pregnancy on the Cardioprotective Effects of
Postconditioning in Male and Female Rats
Fawzi Babiker ,
1
Aishah Al-Jarallah ,
2
and Mariam Al-Awadi
1
1
Department of Physiology, Faculty of Medicine, Health Science Center, Kuwait University, Jabriya, Kuwait
2
Biochemistry, Faculty of Medicine, Health Science Center, Kuwait University, Jabriya, Kuwait
Correspondence should be addressed to Fawzi Babiker; fawzi.b@hsc.edu.kw
Received 15 October 2018; Revised 12 February 2019; Accepted 25 March 2019; Published 6 May 2019
Academic Editor: Vincenzo Russo
Copyright © 2019 Fawzi Babiker et al. is is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Aging, left ventricular hypertrophy (LVH), diabetes mellitus, and pregnancy are well-recognized risk factors that
increase the prevalence of cardio-ischemic events and are linked to poor clinical recovery following acute myocardial infarction. e
coexistence of these risk factors with ischemic heart disease (IHD) deteriorates disease prognosis and could potentially lead to fatal
arrhythmias and heart failure. e objective of this study was to investigate the vulnerability of hearts with aging, LVH, diabetes, and
pregnancy to ischemic insult and their response to pacing postconditioning- (PPC-) induced heart protection. Methods. Hearts
isolated from aged, spontaneously hypertensive and diabetic male and female rats and hearts from pregnant female rats (n � 8 per
group) were subjected to coronary occlusion followed by reperfusion using a modified Langendorff system. Hemodynamics data
were computed digitally, and cardiac damage was accessed by measurements of infarct size and cardiac enzyme release. Results. ere
were no significant differences in the vulnerability of all hearts to ischemic insult compared to their respective controls. PPC
improved cardiac hemodynamics and reduced infarct size and cardiac enzyme release in hearts isolated from aged and spontaneously
hypertensive female rats and female rats with hypertrophied hearts subjected to PPC (P < 0.001). Aged or hypertrophied male hearts
were not protected by PPC maneuver. Moreover, the protective effects of PPC were lost in diabetic male and female hearts although
retained in hearts from pregnant rats. Conclusions. We demonstrate that aging, LVH, diabetes mellitus, and pregnancy do not affect
cardiac vulnerability to ischemic insult. Moreover, PPC mediates cardioprotection in a gender-specific manner in aged and
spontaneously hypertensive rats. Diabetes mellitus provokes the protective effects of PPC on both genders equally. Finally, we
demonstrate that PPC is a new cardioprotective maneuver in hearts from pregnant female rats.
1.Background
Ischemic heart disease (IHD) remains a global health
concern, and acute myocardial infarction continues to be a
leading cause of death [1]. Restriction of coronary blood
supply leads to myocardial infarction which is the primary
determinant of disease prognosis [1]. e infarct size and
disease outcome can remarkably be improved by restoration
of blood flow by reperfusion [2]. However, reperfusion itself
can be devastating resulting in significant damage within the
ischemia-affected area [2]. Several cardioprotective strate-
gies have been developed to limit the destructive effects of
ischemia/reperfusion (I/R) injury on the myocardium. ese
include, but are not limited to, the application of brief
sublethal ischemic episodes at the beginning of reperfu-
sion on-site or a distant vascular bed (ischemic post-
conditioning and remote ischemic postconditioning,
respectively) [3, 4]. More recently, a modification of the
remote postconditioning maneuver has been introduced
which involves changing myocardial stretch pattern via
remote electrical stimulation of the heart chambers (pacing
postconditioning (PPC)) [5]. We have reported that PPC
is an effective protective postconditioning maneuver
against I/R injury in experimental animals [5–7]. We have
further investigated the molecular mechanisms involved in
PPC-induced cardiac protection [8–10]. e first clinical
Hindawi
Cardiology Research and Practice
Volume 2019, Article ID 3403959, 12 pages
https://doi.org/10.1155/2019/3403959