1. Preconditioning withPorphyromonas gingivalislipopolysaccharide may confer cardioprotection and improve recovery of the electrically induced intracellular calcium transient during ischemia and reperfusion
- Author
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S. Wu, K. L. Wong, M. H. M. Fan, Wai K. Leung, T. M. Wong, and Wing-Cheong Yam
- Subjects
Lipopolysaccharides ,Male ,Cardiotonic Agents ,Time Factors ,Heart Ventricles ,Myocardial Infarction ,Myocardial Ischemia ,Ischemia ,Action Potentials ,chemistry.chemical_element ,Myocardial Reperfusion Injury ,Stimulation ,Calcium ,Pharmacology ,Calcium in biology ,Rats, Sprague-Dawley ,Random Allocation ,Cytosol ,Sarcolemma ,medicine ,Animals ,Myocytes, Cardiac ,Calcium Signaling ,Cardioprotection ,business.industry ,Recovery of Function ,medicine.disease ,Myocardial Contraction ,Rats ,Sarcoplasmic Reticulum ,chemistry ,Anesthesia ,Ischemic Preconditioning, Myocardial ,TLR4 ,Periodontics ,Ischemic preconditioning ,Calcium Channels ,business ,Porphyromonas gingivalis ,Injections, Intraperitoneal ,Intracellular - Abstract
Fan MHM, Wong KL, Wu S, Leung WK, Yam WC, Wong TM. Preconditioning with Porphyromonas gingivalis lipopolysaccharide may confer cardioprotection and improve recovery of the electrically induced intracellular calcium transient during ischemia and reperfusion. J Periodont Res 2009; doi: 10.1111/j.1600-0765.2009.01206.x. © 2009 John Wiley & Sons A/S Background and Objective: Porphyromonas gingivalis lipopolysaccharide (LPS) is a ligand for cell surface toll-like receptors (TLR), TLR2 and TLR4 while stimulation of either leads to cardioprotection. We hypothesized that: (1) pretreatment with P. gingivalis LPS at appropriate concentrations would induce cardioprotection against injury induced by ischemia and reperfusion; and (2) P. gingivalis LPS pretreatment at cardioprotective concentrations may reduce Ca2+ overload, which is a precipitating cause of injury, and improve recovery of contractile function. Material and Methods: Male Sprague–Dawley rats were randomly selected to receive intraperitoneal saline or hot phenol–water-extracted P. gingivalis LPS at 0.2, 0.5, 1.0, 2.0 or 4.0 mg/kg 24 h before the experiment. The hearts were isolated and subjected to regional ischemia by coronary artery ligation followed by reperfusion. In isolated rat ventricular myocytes, the cytosolic Ca2+ level and the electrically induced intracellular calcium (E[Ca2+]i) transient, which reflects contractile function, were determined after pretreatment with a cardioprotective dose of P. gingivalis LPS. Results: Pretreatment with 0.5 mg/kg P. gingivalis LPS significantly reduced, while pretreatment with 1.0–4.0 mg/kg significantly increased infarct size. The Ca2+ overload induced by ischemia–reperfusion was attenuated in myocytes from rats pretreated with 0.5 mg/kg P. gingivalis LPS. Pretreated myocytes also showed an increased amplitude of the E[Ca2+]i transient, no prolongation of the time to reach the peak E[Ca2+]i transient and shorter 50% decay time during reperfusion. Conclusion: At a dosage of 0.5 mg/kg, P. gingivalis LPS confers cardioprotection against ischemia–reperfusion-induced injury and improved intracellular E[Ca2+]i transient recovery, hence improving myocyte contractile recovery.
- Published
- 2010
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