Ablation of TRPV1 Abolishes Salicylate-Induced Sympathetic Activity Suppression and Exacerbates Salicylate-Induced Renal Dysfunction in Diet-Induced Obesity

Cells. 2021 May 18;10(5):1234. doi: 10.3390/cells10051234.

Abstract

Sodium salicylate (SA), a cyclooxygenase inhibitor, has been shown to increase insulin sensitivity and to suppress inflammation in obese patients and animal models. Transient receptor potential vanilloid 1 (TRPV1) is a nonselective cation channel expressed in afferent nerve fibers. Cyclooxygenase-derived prostaglandins are involved in the activation and sensitization of TRPV1. This study tested whether the metabolic and renal effects of SA were mediated by the TRPV1 channel. Wild-type (WT) and TRPV1-/- mice were fed a Western diet (WD) for 4 months and received SA infusion (120mg/kg/day) or vehicle for the last 4 weeks of WD feeding. SA treatment significantly increased blood pressure in WD-fed TRPV1-/- mice (p < 0.05) but not in WD-fed WT mice. Similarly, SA impaired renal blood flow in TRPV1-/- mice (p < 0.05) but not in WT mice. SA improved insulin and glucose tolerance in both WT and TRPV1-/- mice on WD (all p < 0.05). In addition, SA reduced renal p65 and urinary prostaglandin E2, prostaglandin F1α, and interleukin-6 in both WT and TRPV1-/- mice (all p < 0.05). SA decreased urine noradrenaline levels, increased afferent renal nerve activity, and improved baroreflex sensitivity in WT mice (all p < 0.05) but not in TRPV1-/- mice. Importantly, SA increased serum creatinine and urine kidney injury molecule-1 levels and decreased the glomerular filtration rate in obese WT mice (all p < 0.05), and these detrimental effects were significantly exacerbated in obese TRPV1-/- mice (all p < 0.05). Lastly, SA treatment increased urine albumin levels in TRPV1-/- mice (p < 0.05) but not in WT mice. Taken together, SA-elicited metabolic benefits and anti-inflammatory effects are independent of TRPV1, while SA-induced sympathetic suppression is dependent on TRPV1 channels. SA-induced renal dysfunction is dependent on intact TRPV1 channels. These findings suggest that SA needs to be cautiously used in patients with obesity or diabetes, as SA-induced renal dysfunction may be exacerbated due to impaired TRPV1 in obese and diabetic patients.

Keywords: TRPV1; afferent renal nerve activity; blood pressure; obesity; renal dysfunction; sodium salicylate.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Baroreflex / drug effects
  • Cyclooxygenase Inhibitors / toxicity*
  • Diet, High-Fat*
  • Disease Models, Animal
  • Energy Metabolism / drug effects
  • Gene Deletion
  • Glomerular Filtration Rate / drug effects
  • Hemodynamics / drug effects
  • Inflammation Mediators / metabolism
  • Insulin Resistance
  • Kidney / drug effects*
  • Kidney / innervation
  • Kidney / metabolism
  • Kidney Diseases / chemically induced*
  • Kidney Diseases / metabolism
  • Kidney Diseases / physiopathology
  • Kidney Diseases / prevention & control
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Obesity / complications
  • Obesity / drug therapy*
  • Obesity / metabolism
  • Obesity / physiopathology
  • Sodium Salicylate / toxicity*
  • Sympathetic Nervous System / drug effects*
  • Sympathetic Nervous System / metabolism
  • Sympathetic Nervous System / physiopathology
  • TRPV Cation Channels / deficiency*
  • TRPV Cation Channels / genetics

Substances

  • Cyclooxygenase Inhibitors
  • Inflammation Mediators
  • TRPV Cation Channels
  • TRPV1 protein, mouse
  • Sodium Salicylate