Arachidonic acid metabolites follow the preferential course of cyclooxygenase pathway for the basal tone in the internal anal sphincter

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 296; no. 4; pp. G727 - G734
• Main Authors: de Godoy, Márcio A F, Rattan, Neeru, Rattan, Satish
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.04.2009
• Subjects: Anal Canal - drug effects; Anal Canal - physiology; Animals; Arachidonate 5-Lipoxygenase - metabolism; Arachidonic Acid - metabolism; Cyclooxygenase Inhibitors - pharmacology; Dose-Response Relationship, Drug; Enzymes; Fatty acids; Gene Expression Regulation, Enzymologic - physiology; Hormones and Signaling; In Vitro Techniques; Lipids; Lipoxygenase Inhibitors - pharmacology; Male; Metabolism; Muscle Contraction - drug effects; Muscle Contraction - physiology; Muscle, Smooth - drug effects; Muscle, Smooth - physiology; Physiology; Prostaglandin-Endoperoxide Synthases - metabolism; Rats; Rats, Sprague-Dawley; RNA, Messenger - genetics; RNA, Messenger - metabolism; Signal transduction; Signal Transduction - drug effects; Signal Transduction - physiology
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.90707.2008

Present studies determined the roles of the cyclooxygenase (COX) versus the lipoxygenase (LO) pathways in the metabolic pathway of arachidonic acid (AA) in the internal anal sphincter (IAS) tone. Studies were performed in the rat IAS versus the nontonic rectal smooth muscle (RSM). Indomethacin, the dual COX inhibitor, but not nordihydroguaiaretic acid (NDGA), the LO inhibitor, produced a precipitous decrease in the IAS tone. However, when added in the background of indomethacin, NDGA caused significant reversal of the IAS tone. These inhibitors had no significant effect on the RSM. To follow the significance of COX versus LO pathways, we examined the effects of AA and its metabolites. In the IAS, AA caused an increase in the IAS tone (Emax=38.8+/-3.0% and pEC50=3.4+/-0.1). In the RSM, AA was significantly less efficacious and potent (Emax=11.3+/-3.5% and pEC50=2.2+/-0.3). The AA metabolites (via COXs) PGF2alpha and U-46619 (a stable analog of thromboxane A2) produced increases in the IAS tone and force in the RSM. Conversely, AA metabolites (via 5-LO) lipoxin A4, 5-HETE, and leukotriene C4 decreased the IAS tone. Finally, the contractile effects of AA in the IAS were selectively attenuated by the COX-1 but not the COX-2 inhibitor. Collectively, the specific effects of AA and the COX inhibitor, the Western blot and RT-PCR analyses showing specifically higher levels of COX-1, suggest a preferential role of the COX (specifically COX-1) pathway versus the LO in the regulation of the IAS tone.