Trimethylamine, a gut bacteria metabolite and air pollutant, increases blood pressure and markers of kidney damage including proteinuria and KIM-1 in rats

• Published in: Journal of translational medicine 2022-10, Vol.20 (1), p.1-470, Article 470
• Main Authors: Maksymiuk, Klaudia M, Szudzik, Mateusz, GawryÅ-KopczyÅska, Marta, Onyszkiewicz, Maksymilian, Samborowska, Emilia, Mogilnicka, Izabella, Ufnal, Marcin
• Format: Article
• Language: English
• Subjects: Air pollution; Analysis; Angiotensin; Animals; Arteries; Arterioles; Blood pressure; Body weight; Chronic exposure; Chronic kidney disease; Chronic kidney failure; Complications and side effects; Control; Creatinine; Degeneration; Disease; Electrolyte balance; Excretion; Flavin; Heart failure; Hemodynamics; Hypertension; Hypertrophy; Identification and classification; Intestinal microflora; Kidney damage; Kidneys; Laboratories; Liver; Metabolism; Metabolites; Microbiota; Microbiota (Symbiotic organisms); Plasma; Pollutants; Prevention; Proteins; Proteinuria; Renin; Risk factors; Serum levels; Trimethylamine; Trimethylamine oxide; Urine
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-022-03687-y

Background Trimethylamine oxide (TMAO) is a biomarker in cardiovascular and renal diseases. TMAO originates from the oxidation of trimethylamine (TMA), a product of gut microbiota and manufacturing industries-derived pollutant, by flavin monooxygenases (FMOs). The effect of chronic exposure to TMA on cardiovascular and renal systems is undetermined. Methods Metabolic, hemodynamic, echocardiographic, biochemical and histopathological evaluations were performed in 12-week-old male SPRD rats receiving water (controls) or TMA (200 or 500 [micro]M/day) in water for 18 weeks. TMA and TMAO levels, the expression of FMOs and renin-angiotensin system (RAS) genes were evaluated in various tissues. Results In comparison to controls, rats receiving high dose of TMA had significantly increased arterial systolic blood pressure (126.3 [+ or -] 11.4 vs 151.2 [+ or -] 19.9 mmHg; P = 0.01), urine protein to creatinine ratio (1.6 (1.5; 2.8) vs 3.4 (3.3; 4.2); P = 0.01), urine KIM-1 levels (2338.3 [+ or -] 732.0 vs. 3519.0 [+ or -] 953.0 pg/mL; P = 0.01), and hypertrophy of the tunica media of arteries and arterioles (36.61 [+ or -] 0.15 vs 45.05 [+ or -] 2.90 [micro]m, P = 0.001 and 18.44 [+ or -] 0.62 vs 23.79 [+ or -] 2.60 [micro]m, P = 0.006; respectively). Mild degeneration of renal bodies with glomerulosclerosis was also observed. There was no significant difference between the three groups in body weight, water-electrolyte balance, echocardiographic parameters and RAS expression. TMA groups had marginally increased 24 h TMA urine excretion, whereas serum levels and 24 h TMAO urine excretion were increased up to 24-fold, and significantly increased TMAO levels in the liver, kidneys and heart. TMA groups had lower FMOs expression in the kidneys. Conclusions Chronic exposure to TMA increases blood pressure and increases markers of kidney damage, including proteinuria and KIM-1. TMA is rapidly oxidized to TMAO in rats, which may limit the toxic effects of TMA on other organs. Keywords: Trimethylamine, Trimethylamine oxide, Chronic kidney disease, Hypertension, Proteinuria, Kidney damage