Skip to main content

Advertisement

Log in

Urethane suppresses rat lung inducible cyclooxygenase and nitric oxide synthase mRNA levels

  • Published:
Inflammation Research Aims and scope Submit manuscript

Abstract.

Objective and Design: The purpose of the present study was to evaluate the effect of urethane, pentobarbital sodium and ketamine-xylazine anesthesia upon constitutive and inducible cyclooxygenase (COX-1; COX-2) and nitric oxide synthase (eNOS; iNOS) mRNA levels in the lung.¶Methods: mRNA levels were determined by the semiquantitative RT-PCR technique.¶Treatment: Urethane (1.1g/kg ip), Pentobarbital Sodium (40 mg/kg ip), and ketamine (85 mg/kg) - xylazine (15 mg/ kg, im). Non-anesthetized animals served as controls.¶Material: Sprague-Dawley rat lungs¶Results: Urethane significantly decreased COX-1 and COX-2 mRNA levels to 30% of control values. This agent had no effect upon eNOS, but completely suppressed iNOS mRNA levels. Pentobarbital sodium and ketamine had no effect on the mRNA levels for COX-1 and COX-2 the lung.¶Conclusions: Urethane has a suppressive effect on COX and iNOS RNA message in the lung and for this reason it should be avoided as an anesthetic when lung inflammatory processes are experimentally evaluated in the rat.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received 7 April 2000; returned for revision 21 June 2000; accepted by G. Letts 10 July 2000

Rights and permissions

Reprints and permissions

About this article

Cite this article

Martinez, F., Harabor, A., Amankwah, E. et al. Urethane suppresses rat lung inducible cyclooxygenase and nitric oxide synthase mRNA levels. Inflamm. res. 49, 727–731 (2000). https://doi.org/10.1007/s000110050653

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s000110050653

Navigation