Indole and indoxyl sulfate, gut bacteria metabolites of tryptophan, change arterial blood pressure via peripheral and central mechanisms in rats. (April 2018)

• Record Type: Journal Article
• Authors: Huć, Tomasz; Nowinski, Artur; Drapala, Adrian; Konopelski, Piotr; Ufnal, Marcin
• Is Part Of: Pharmacological research. Volume 130(2018)
• Page Start: 172
• Page End: 179
• Publication Date: 2018-04
• Subjects: BP arterial blood pressure -- b.w. body weight -- CVOs circumventricular organs -- ICV intracerebroventricular -- Indoxyl indoxyl sulfate -- IV administered into the femoral vein -- MABP mean arterial blood pressure -- HR heart rate -- OND ondansetron -- PIZ pizotifen -- FLU flupentixol; indole (1H-indole) -- indoxyl sulfate (potassium 1H-indol-3-yl sulfate) -- pizotifen -- ondansetron -- cis-(Z)-flupenthixol dihydrochloride; Indole -- Gut bacteria -- Metabolites -- Arterial blood pressure -- Serotonin receptors; Pharmacology -- Periodicals; Pharmacology -- Periodicals; Research -- Periodicals; Médicaments -- Recherche -- Périodiques; Pharmacologie -- Périodiques; 615.105
• DOI: 10.1016/j.phrs.2017.12.025
• Languages: English
• ISSNs: 1043-6618

Abstract

Graphical abstract: Abstract: Arterial blood pressure (BP) is regulated by a complex network of peripheral and central (brain) mechanisms. Research suggests that gut bacteria-derived compounds may affect the circulatory system. We evaluated hemodynamic effects of indole, a gut bacteria-derived product of tryptophan, and indoxyl sulfate (indoxyl), a liver metabolite of indole. BP and heart rate (HR) were recorded in anesthetized, male, Wistar rats at baseline and after the administration of either a vehicle, indole, or indoxyl into the femoral vein (IV) or into the lateral ventricle of the brain (ICV). Besides, we evaluated the effect of pretreatment with flupentixol, a non-selective D1, D2, α1 and 5 HT2A receptor blocker; pizotifen, a non-selective 5-HT1, 5-HT2A and 5HT2C receptor blocker; and ondansetron, a 5-HT3 blocker, on hemodynamic responses to indole and indoxyl. Vehicle infused IV and ICV did not affect hemodynamics. Indole administered IV produced a dose-dependent increase in BP but not HR. In contrast, the ICV infusion of indole produced a decrease in BP and HR. Indoxyl infused IV produced an increase in BP and HR, whereas indoxyl infused ICV did not affect BP and HR. The hemodynamic effects of indole and indoxyl were inhibited by pretreatment with ondansetron and pizotifen but not flupentixol. In conclusion, indole and indoxyl sulfate affect arterial blood pressure via peripheral and central mechanisms dependent on serotonin signalling. We propose that indole and indoxyl sulfate may be mediators in the interaction between gut bacteria and the circulatory system.