HCN as a Mediator of Urinary Homeostasis: Age-Associated Changes in Expression and Function in Adrenergic Detrusor Relaxation

J Gerontol A Biol Sci Med Sci. 2019 Feb 15;74(3):325-329. doi: 10.1093/gerona/gly137.

Abstract

The Hyperpolarization activated, cyclic nucleotide gated (HCN) channel is a candidate mediator of neuroendocrine influence over detrusor tonus during filling. In other tissues, HCN loss with aging is linked to declines in rhythmicity and function. We hypothesized that HCN has an age-sensitive expression profile and functional role in adrenergic bladder relaxation. HCN was examined in bladders from young (2-6 months) and old (18-24 months) C57BL/6 female mice, using qRT-PCR, RNAScope, and Western blots. Isometric tension studies were conducted using bladder strips from young wild-type (YWT), old wild-type (OWT), and young HCN1 knock-out (YKO) female mice to test the role HCN in effects of β-adrenergic stimulation. Hcn1 is the dominant HCN isoform RNA in the mouse bladder wall, and is diminished with age. Location of Hcn RNA within the mouse bladder wall is isoform-specific, with HCN1 limited to the detrusor layer. Passively-tensioned YWT bladder strips are relaxed by isoproterenol in the presence of HCN function, where OWT strips are relaxed only in the presence of HCN blockade. HCN has an age-specific expression and function in adrenergic detrusor relaxation in mouse bladder strips.

Keywords: Aging; Bladder physiology; Detrusor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Animals
  • Female
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels / metabolism*
  • Isoproterenol / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Muscle Relaxation / drug effects
  • Muscle Relaxation / physiology*
  • Muscle Tonus / drug effects
  • Muscle Tonus / physiology*
  • Tissue Culture Techniques
  • Urinary Bladder / metabolism*
  • Urinary Bladder / physiopathology*

Substances

  • Adrenergic beta-Agonists
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Isoproterenol