ISSN:
1432-1912
Keywords:
Key words Rhinitis
;
Leukotrienes
;
5-Lipoxygenase
;
Histamine
;
TMK-688
;
Anti-allergic Drug
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract TMK688 (1-[{5’-(3”-methoxy-4”-ethoxy-carbonyloxyphenyl)-2’,4’-pentadienoyl} aminoethyl]-4-diphenylmethoxypiperidine) is being developed as an orally effective antiallergic drug having both 5-lipoxy-genase inhibitory activity and anti-histamine activity (Shizawa et al. 1996; Tohda et al. 1997). The efficacy of TMK688 against allergic rhinitis was examined in passively sensitized guinea pigs. TMK688 inhibited the increase in intranasal resistance following antigen challenge at doses of 1 and 3.2mg/kg p.o. The allergic nasal obstruction was also suppressed by 10mg/kg i.v. of FPL-55712, a peptide leukotriene receptor antagonist, but not by 3.2mg/kg i.v. pyrilamine, a histamine H1 receptor antagonist, or by 10mg/kg p.o. of ketotifen, an anti-allergic drug having anti-histamine activity, suggesting that the nasal obstruction was caused by leukotrienes. Following antigen challenge, the intranasal release of leukotrienes B4 and C4, and histamine increased in passively sensitized guinea pigs. TMK688 tended to suppress the increase in immunoreactive leukotrienes B4 and C4 in the nasal lavage fluid at a dose of 1mg/kg p.o., and significantly inhibited the increase at 3.2mg/kg. The brilliant blue dye leakage following antigen challenge from the blood stream into the na-sal cavities was significantly inhibited by not only TMK688 and FPL-55712 but also pyrilamine, suggesting that the allergic dye leakage was caused cooperatively by leukotrienes and histamine. However, keto-tifen showed no significant suppression of the dye leakage even at 10mg/kg p.o., although this drug inhibited the histamine-induced dye leakage at far lower doses (0.1mg/kg p.o. or higher) in unsensitized guinea pigs. Therefore, histamine is not necessarily the major mediator of allergic dye leakage in our experiment. These findings demonstrate that TMK688 may be superior to antihistamines as a therapeutic agent for allergic rhinitis.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/PL00005122
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