Department of Medicinal Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama , Japan.
Biol Pharm Bull. 2010;33(1):64-6. doi: 10.1248/bpb.33.64.
The aim of the present study was to clarify the involvement of prostaglandin E(2) (PGE(2)) in nasal congestion in Brown Norway (BN) rats. For this purpose, we studied the effects of PGE(2) receptor (EP(1), EP(2), EP(3) and EP(4)) agonists on nasal congestion and sneezing induced by toluene 2,4-diisocyanate (TDI). Enhanced pause (Penh) was increased 1 h (early phase) and 4 h (late phase) after TDI challenge. Sulprostone (an EP(3) receptor agonist) inhibited the increase of Penh, an index of nasal congestion, in both early and late phase responses. On the other hand, PGE(1) alcohol (an EP(4) agonist) increased Penh in the early phase response. Moreover, sulprostone inhibited sneezing, an immediate response by TDI challenge. These results indicate that EP(3) receptor is responsible for the relief of nasal congestion in both early and late phase responses, and EP(4) receptor is correlated with the development of nasal congestion in the early phase response. In addition, EP(3) receptor also participates in sneezing in allergic rhinitis induced by TDI challenge in BN rats.
本研究旨在阐明前列腺素 E2(PGE2)在褐家鼠(BN)鼻塞中的作用。为此,我们研究了 PGE2 受体(EP1、EP2、EP3 和 EP4)激动剂对甲苯 2,4-二异氰酸酯(TDI)诱导的鼻塞和打喷嚏的影响。增强呼气暂停(Penh)在 TDI 挑战后 1 小时(早期)和 4 小时(晚期)增加。舒普洛酮(EP3 受体激动剂)抑制了早期和晚期反应中 Penh 的增加,Penh 是鼻塞的一个指标。另一方面,PGE1 酒精(EP4 激动剂)增加了早期反应中的 Penh。此外,舒普洛酮抑制了 TDI 挑战引起的立即反应打喷嚏。这些结果表明,EP3 受体负责缓解早期和晚期反应中的鼻塞,而 EP4 受体与早期反应中鼻塞的发展有关。此外,EP3 受体还参与了由 TDI 挑战引起的 BN 大鼠过敏性鼻炎中的打喷嚏。