Literature DB >> 10869473

Purified fumonisin B(1) decreases cardiovascular function but does not alter pulmonary capillary permeability in swine.

G W Smith1, P D Constable, R M Eppley, M E Tumbleson, L A Gumprecht, W M Haschek-Hock.   

Abstract

Fumonisins are mycotoxins produced by Fusarium verticillioides, which induce acute pulmonary edema in swine. We previously reported that ingestion of fumonisin-containing culture material decreases cardiovascular function in swine (1996,a,b; Fundam. Appl. Toxicol. 31, 169-172; 33, 140-148; 1999, Am. J Vet. Res. 60, 1291-1300). The main purpose of this study was to confirm that fumonisin B(1) was responsible for the observed cardiovascular changes. Treated pigs (n = 6) were given daily intravenous injections of purified fumonisin B(1) at 1 mg/kg for 4 days, while controls (n = 6) were injected with equal volumes of saline. On day 5, pigs were anesthetized with butorphanol-chloralose and instrumented for hemodynamic studies. Terminally, bronchoalveolar lavage was performed on each pig to determine the relative permeability index of the pulmonary endothelium. Fumonisin B(1)-treated pigs had marked decreases in the maximal rate of change of left ventricular pressure (dP/dt(max)), mean aortic pressure, cardiac output, and arterial pO(2), accompanied by increases in mean pulmonary artery pressure, oxygen extraction ratio, and blood hemoglobin concentration. Plasma and left ventricular sphingosine and sphinganine concentrations were markedly increased in treated pigs at day 5; however, there was no difference in the relative permeability index between groups. Serum cholesterol concentrations and activities of hepatic-derived enzymes were increased, and hepatocyte apoptosis and mitoses were present in the livers of fumonisin-treated pigs. In the lungs of treated pigs, there was proteinaceous edema and membranous accumulations in capillary endothelial cells. These results indicate that cardiovascular function is altered by fumonisin B(1), and that fumonisin-induced pulmonary edema is caused by left-sided heart failure and not by altered endothelial permeability. Because of the potential for contamination of human foodstuffs by fumonisins, the cardiovascular toxicity of these compounds must be taken into consideration.

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Year:  2000        PMID: 10869473     DOI: 10.1093/toxsci/56.1.240

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  4 in total

1.  The African Fusarium/maize disease.

Authors:  Michael F Dutton
Journal:  Mycotoxin Res       Date:  2009-01-14       Impact factor: 3.833

Review 2.  Fumonisin toxicosis in swine: an overview of porcine pulmonary edema and current perspectives.

Authors:  W M Haschek; L A Gumprecht; G Smith; M E Tumbleson; P D Constable
Journal:  Environ Health Perspect       Date:  2001-05       Impact factor: 9.031

3.  Mycotoxin Fumonisin B1 Interferes Sphingolipid Metabolisms and Neural Tube Closure during Early Embryogenesis in Brown Tsaiya Ducks.

Authors:  Chompunut Lumsangkul; Ko-Hua Tso; Yang-Kwang Fan; Hsin-I Chiang; Jyh-Cherng Ju
Journal:  Toxins (Basel)       Date:  2021-10-20       Impact factor: 4.546

Review 4.  Research Progress on Fumonisin B1 Contamination and Toxicity: A Review.

Authors:  Jia Chen; Jun Wen; Yating Tang; Jichao Shi; Guodong Mu; Rong Yan; Jing Cai; Miao Long
Journal:  Molecules       Date:  2021-08-29       Impact factor: 4.411

  4 in total

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