Literature DB >> 20378750

ST depression, arrhythmia, vagal dominance, and reduced cardiac micro-RNA in particulate-exposed rats.

Aimen K Farraj1, Mehdi S Hazari, Najwa Haykal-Coates, Christina Lamb, Darrell W Winsett, Yue Ge, Allen D Ledbetter, Alex P Carll, Maribel Bruno, Andy Ghio, Daniel L Costa.   

Abstract

Recently, investigators demonstrated associations between fine particulate matter (PM)-associated metals and adverse health effects. Residual oil fly ash (ROFA), a waste product of fossil fuel combustion from boilers, is rich in the transition metals Fe, Ni, and V, and when released as a fugitive particle, is an important contributor to ambient fine particulate air pollution. We hypothesized that a single-inhalation exposure to transition metal-rich PM will cause concentration-dependent cardiovascular toxicity in spontaneously hypertensive (SH) rats. Rats implanted with telemeters to monitor heart rate and electrocardiogram were exposed once by nose-only inhalation for 4 hours to 3.5 mg/m(3), 1.0 mg/m(3), or 0.45 mg/m(3) of a synthetic PM (dried salt solution), similar in composition to a well-studied ROFA sample consisting of Fe, Ni, and V. Exposure to the highest concentration of PM decreased T-wave amplitude and area, caused ST depression, reduced heart rate (HR), and increased nonconducted P-wave arrhythmias. These changes were accompanied by increased pulmonary inflammation, lung resistance, and vagal tone, as indicated by changes in markers of HR variability (increased root of the mean of squared differences of adjacent RR intervals [RMSSD], low frequency [LF], high frequency [HF], and decreased LF/HF), and attenuated myocardial micro-RNA (RNA segments that suppress translation by targeting messenger RNA) expression. The low and intermediate concentrations of PM had less effect on the inflammatory, HR variability, and micro-RNA endpoints, but still caused significant reductions in HR. In addition, the intermediate concentration caused ST depression and increased QRS area, whereas the low concentration increased the T-wave parameters. Thus, PM-induced cardiac dysfunction is mediated by multiple mechanisms that may be dependent on PM concentration and myocardial vulnerability (this abstract does not reflect the policy of the United States Environmental Protection Agency).

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Year:  2010        PMID: 20378750     DOI: 10.1165/rcmb.2009-0456OC

Source DB:  PubMed          Journal:  Am J Respir Cell Mol Biol        ISSN: 1044-1549            Impact factor:   6.914


  30 in total

1.  Whole and particle-free diesel exhausts differentially affect cardiac electrophysiology, blood pressure, and autonomic balance in heart failure-prone rats.

Authors:  Alex P Carll; Mehdi S Hazari; Christina M Perez; Quentin Todd Krantz; Charly J King; Darrell W Winsett; Daniel L Costa; Aimen K Farraj
Journal:  Toxicol Sci       Date:  2012-04-26       Impact factor: 4.849

2.  Ambient particulate air pollution and microRNAs in elderly men.

Authors:  Serena Fossati; Andrea Baccarelli; Antonella Zanobetti; Mirjam Hoxha; Pantel S Vokonas; Robert O Wright; Joel Schwartz
Journal:  Epidemiology       Date:  2014-01       Impact factor: 4.822

3.  Individual PM2.5 exposure is associated with the impairment of cardiac autonomic modulation in general residents.

Authors:  Yuquan Xie; Liang Bo; Shuo Jiang; Zhenyong Tian; Haidong Kan; Yigang Li; Weimin Song; Jinzhuo Zhao
Journal:  Environ Sci Pollut Res Int       Date:  2016-02-24       Impact factor: 4.223

4.  Air toxics and epigenetic effects: ozone altered microRNAs in the sputum of human subjects.

Authors:  Rebecca C Fry; Julia E Rager; Rebecca Bauer; Elizabeth Sebastian; David B Peden; Ilona Jaspers; Neil E Alexis
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-04-25       Impact factor: 5.464

5.  Acute peat smoke inhalation sensitizes rats to the postprandial cardiometabolic effects of a high fat oral load.

Authors:  Brandi L Martin; Leslie C Thompson; Yongho Kim; Wanda Williams; Samantha J Snow; Mette C Schladweiler; Pamela Phillips; Charly King; Judy Richards; Najwa Haykal-Coates; Mark Higuchi; M Ian Gilmour; Urmila P Kodavanti; Mehdi S Hazari; Aimen K Farraj
Journal:  Sci Total Environ       Date:  2018-06-22       Impact factor: 7.963

6.  TRPA1 mediates changes in heart rate variability and cardiac mechanical function in mice exposed to acrolein.

Authors:  Nicole Kurhanewicz; Rachel McIntosh-Kastrinsky; Haiyan Tong; Allen Ledbetter; Leon Walsh; Aimen Farraj; Mehdi Hazari
Journal:  Toxicol Appl Pharmacol       Date:  2016-10-13       Impact factor: 4.219

Review 7.  The Role of MicroRNAs in Environmental Risk Factors, Noise-Induced Hearing Loss, and Mental Stress.

Authors:  Verónica Miguel; Julia Yue Cui; Lidia Daimiel; Cristina Espinosa-Díez; Carlos Fernández-Hernando; Terrance J Kavanagh; Santiago Lamas
Journal:  Antioxid Redox Signal       Date:  2017-06-30       Impact factor: 8.401

8.  Acrolein decreases endothelial cell migration and insulin sensitivity through induction of let-7a.

Authors:  Timothy E O'Toole; Wesley Abplanalp; Xiaohong Li; Nigel Cooper; Daniel J Conklin; Petra Haberzettl; Aruni Bhatnagar
Journal:  Toxicol Sci       Date:  2014-05-08       Impact factor: 4.849

9.  Hypoxia stress test reveals exaggerated cardiovascular effects in hypertensive rats after exposure to the air pollutant acrolein.

Authors:  Christina M Perez; Allen D Ledbetter; Mehdi S Hazari; Najwa Haykal-Coates; Alex P Carll; Darrell W Winsett; Daniel L Costa; Aimen K Farraj
Journal:  Toxicol Sci       Date:  2013-01-18       Impact factor: 4.849

10.  Altered microRNA profiles in bronchoalveolar lavage fluid exosomes in asthmatic patients.

Authors:  Bettina Levänen; Nirav R Bhakta; Patricia Torregrosa Paredes; Rebecca Barbeau; Stefanie Hiltbrunner; Joshua L Pollack; C Magnus Sköld; Magnus Svartengren; Johan Grunewald; Susanne Gabrielsson; Anders Eklund; Britt-Marie Larsson; Prescott G Woodruff; David J Erle; Åsa M Wheelock
Journal:  J Allergy Clin Immunol       Date:  2013-01-16       Impact factor: 10.793

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