Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes the procedure for measuring ATP concentrations in the lumen of the bladder in an anesthetized rodent.

Abstract

ATP, released from the urothelium in response to bladder distension, is thought to play a significant sensory role in the control of micturition. Therefore, accurate measurement of urothelial ATP release in a physiological setting is an important first step in studying the mechanisms that control purinergic signaling in the urinary bladder. Existing techniques to study mechanically evoked urothelial ATP release utilize cultured cells plated on flexible supports or bladder tissue pinned into Ussing chambers; however, each of these techniques does not fully emulate conditions in the intact bladder. Therefore, an experimental setup was developed to directly measure ATP concentrations in the lumen of the rodent urinary bladder.

In this setup, the bladders of anesthetized rodents are perfused through catheters in both the dome of the bladder and via the external urethral orifice. Pressure in the bladder is increased by capping the urethral catheter while perfusing sterile fluid into the bladder through the dome. Measurement of intravesical pressure is achieved using a pressure transducer attached to the bladder dome catheter, akin to the setup used for cystometry. Once the desired pressure is reached, the urethral catheter's cap is removed, and fluid collected for ATP quantification by luciferin-luciferase assay. Through this experimental setup, the mechanisms controlling both mechanical and chemical stimulation of urothelial ATP release can be interrogated by including various agonists or antagonists into the perfusate or by comparing results between wildtype and genetically modified animals.

Introduction

Urinary ATP is thought to play a significant sensory role in the control of micturition1. For example, it is thought that ATP is released from the urothelium in response to distension where it can act on receptors on bladder afferent nerves to increase their excitability, leading to sensations of fullness2. Thus, it is also thought that urinary ATP could be an important player in the development of bladder pathologies. In support of this hypothesis, urinary ATP concentrations are significantly increased in patients suffering from overactive bladder (OAB)3, bladder pain syndrome/interstitial cystit....

Protocol

All procedures carried out in rodents must adhere to the applicable guidelines and be approved by the local institutional ethics review committee. The experiments performed for this manuscript were carried out in accordance with the National Research Council's Guide for the Care and Use of Laboratory Animals and approved by the Institutional Animal Care and Use Committee (IACUC) of the University of Pittsburgh School of Medicine. See Figure 1 for a modified version of the standard rodent.......

Representative Results

The described protocol allows for the accurate measurement of urothelial ATP release in vivo from the lumen of the bladder, using a modified version of the standard rodent cystometry setup (see Figure 1). This allows the researcher to examine the effects of drugs on stretch-mediated ATP release in a physiological setting.

figure-representative results-459

Discussion

The majority of research into urothelial ATP release is conducted in cultured cells, using either immortalized cell lines or primary cultures of rodent urothelial cells. While these models have the benefit of being relatively high throughput (i.e., one culture/passage can make many plates/dishes of cells), their physiological relevance is diminished due to: 1) the inability of urothelial cells to grow polarized unless they are grown on special supports and 2) the difficulty in exposing cultured cells to physiological lev.......

Acknowledgements

This work was supported by a grant from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) to JMB (DK117884).

....

Materials

NameCompanyCatalog NumberComments
amplifierWorld Precision Instruments (WPI)SYS-TBM4M
ATP assay kitSigma-Aldrich, Inc.FLAA-1KT
data acquisition system/ softwareDataQ InstrumentsDI-1100Software included, requires Windows-based computer
Hexamethonium bromideSigma-Aldrich, Inc.H087920 mg/kg dose
IsofluraneCovetrus North America29404
lidocaineCovetrus North America2468
Luer Lock plugsFisher ScientificNC0455253
luminometer (GloMax 20/20)PromegaE5311
Polyethylene (PE50) tubingFisher Scientific14-170-12B
Pump 33 DDS syringe pumpHarvard Apparatus703333
pressure transducersWorld Precision Instruments (WPI)BLPR2
surgical instruments (scissors, hemostats, forceps, etc.)Fine Science Toolsmultiple numbers
surgical lubricantFisher Scientific10-000-694
Sur-Vet I.V. catheter Covetrus North America5060320 G x 1 inch
tiltable surgical table (Plas Labs)Fisher Scientific01-288-30A
Tubing connectorsFisher Scientific14-826-19Eallows Luer-Lock connectors to attach to tubing
UrethaneSigma-Aldrich, Inc.U25000.5 g/mL conc., 1.2 g/kg dose

References

  1. Burnstock, G. Purinergic signalling in the urinary tract in health and disease. Purinergic Signalling. 10 (1), 103-155 (2014).
  2. Birder, L. A. Urothelial signaling. Autonomic Neuroscience: Basic & Clinical. 153 (1-2), 33-4....

Explore More Articles

Artificial IntelligenceAI Writing AssistantsContent GenerationCopywritingText GenerationAI powered Writing

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved