Citation

Zhao Q, Yan T, Li L, Chopp M, Venkat P, Qian Y, Li R, Wu R, Li W, Lu M, Zhang T, Chen J. J. Neurotrauma 2019; 36(4): 619-629.

Affiliation

Henry Ford Hospital, Neurology, Detroit, Michigan, United States ; jieli@neuro.hfh.edu.

Copyright

(Copyright © 2019, Mary Ann Liebert Publishers)

DOI

10.1089/neu.2018.5766

PMID

30045672

Abstract

Cardiovascular complications are common after TBI and are associated with increased morbidity and mortality. In this study, we investigated the possible role of the immune system in mediating cardiac dysfunction post-TBI in mice. Adult male C57BL/6J mice were subjected to a TBI model of controlled cortical impact (CCI) with or without splenectomy (n=20/group). Splenectomy was performed immediately prior to induction of TBI. Cardiac function was measured using echocardiography prior to and after TBI. Neurological and cognitive functional tests and flow cytometry and immunostaining were performed. TBI mice exhibited significant cardiac dysfunction identified by decreased left ventricular ejection fraction (LVEF) and fractional shortening (FS) at 3 and 30 days post-TBI. In addition, these mice exhibited significantly increased cardiomyocyte apoptosis, inflammation and oxidative stress at 3 and 30 days post-TBI, as well as cardiac hypertrophy and fibrosis, and ventricular dilatation at 30 days after TBI. TBI mice subjected to splenectomy showed significantly improved cardiac function, and decreased cardiac fibrosis, oxidative stress, cardiomyocyte apoptosis, as well as decreased infiltration of immune cells and inflammatory factor expression in the heart compared to TBI control mice. TBI mice exhibited severe neurological and cognitive function deficits. However, splenectomy did not improve neurological and cognitive functional outcome after TBI compared with the TBI control group. TBI induces immune cells infiltration and inflammatory factor expression in the heart as well as cardiac dysfunction. Splenectomy decreases heart inflammation and improves cardiac function after TBI. Immune response may contribute to TBI-induced cardiac dysfunction.

Language: en

Keywords

ANIMAL STUDIES; IN VIVO STUDIES; Immune response; Splenectomy; TRAUMATIC BRAIN INJURY; Traumatic brain injury; cardiac- dysfunction brain-heart interaction.; controlled cortical impact