Altered phosphorylation and calcium sensitivity of cardiac myofibrillar proteins during sepsis

Author:

Wu Li-Ling1,Tang Chaoshu2,Liu Maw-Shung3

Affiliation:

1. Department of Physiology and Pathophysiology, Peking University Health Sciences Center, Beijing 100083;

2. Institute of Cardiovascular Diseases, Peking University First Hospital, Beijing 100034, China; and

3. Department of Pharmacological and Physiological Science, Saint Louis University School of Medicine, St. Louis, Missouri 63104

Abstract

Altered phosphorylation and Ca2+ sensitivity of cardiac myofibrillar proteins during different phases of sepsis were investigated. Sepsis was induced by cecal ligation and puncture (CLP). The results show that phosphorylation of troponin I (TnI) was increased by 268% during the early phase (9 h after CLP) but decreased by 46% during the late phase (18 h after CLP) of sepsis. Phosphorylation of C protein was increased by 76% during the early phase but decreased by 41% during the late phase of sepsis. Phosphorylation of myosin light chain-2 (MLC-2) remained unaltered during the early phase but was decreased by 38% during the late phase of sepsis. Phosphorylation of TnT was unaffected during the progression of sepsis. The increases in the phosphorylation of TnI and C protein during early sepsis were associated with the decrease in the Ca2+ sensitivity of myofilaments and the increases in myocardial changes in tension development (+dP/d t max) and cAMP level. The decreases in the phosphorylation of TnI and C protein during late sepsis coincided with the declines in the activities of myofibrillar ATPase, Ca2+ sensitivity of myofilaments, myocardial ±dP/d t max, and cAMP content. The increases and the decreases in the phosphorylation of TnI and C protein, ±dP/d t max, and the tissue cAMP level were sensitive to isoproterenol stimulation and propranolol inhibition. These findings suggest that alterations in the phosphorylation of myofibrillar proteins, such as TnI, C protein, and MLC-2, and changes in the activities and the Ca2+ sensitivity of myofibrillar ATPase may contribute to the altered cardiac function during the progression of sepsis. Furthermore, the sepsis-induced alterations in the phosphorylation and Ca2+ sensitivity of cardiac myofibrillar proteins were mediated via a β-adrenergic receptor pathway.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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