Department of Pharmacology, Kyoto Pharmaceutical University, Nakauchi, Misasagi, Yamashina, Japan.
Prostaglandins Other Lipid Mediat. 2011 Aug;95(1-4):27-34. doi: 10.1016/j.prostaglandins.2011.05.001. Epub 2011 May 10.
Although it has been suggested that prostaglandin (PG) D(2) is involved in the pathogenesis of allergic rhinitis, whether the inhibition of hematopoietic PGD(2) synthase (H-PGDS) shows beneficial effects on allergic rhinitis has been unclear. We evaluated the effects of a selective H-PGDS inhibitor, TFC-007, on nasal symptoms on Japanese cedar pollen-induced allergic rhinitis of guinea pigs. Sensitized animals were challenged with the pollen once a week. TFC-007 (30mg/kg, p.o.) given once before a challenge almost completely suppressed PGD(2) production in the nasal tissue early and late after the challenge. Although pre-treatment did not affect the incidences of sneezing and early phase nasal blockage, late phase nasal blockage was partially but significantly attenuated; however, nasal eosinophilia was not suppressed. In contrast, when TFC-007 was given once 1.5h after the challenge, the late phase response was not affected. Collectively, PGD(2) produced by H-PGDS early after an antigen challenge can participate in the induction of late phase nasal blockage, although the mechanism may be independent of eosinophil infilatration. The strategy for H-PGDS inhibition may be beneficial for allergic rhinitis therapy.
尽管已经有人提出前列腺素(PG)D(2)参与了过敏性鼻炎的发病机制,但抑制造血 PGDS(H-PGDS)是否对过敏性鼻炎有有益作用尚不清楚。我们评估了一种选择性 H-PGDS 抑制剂 TFC-007 对豚鼠日本雪松花粉诱导的过敏性鼻炎的鼻部症状的影响。致敏动物每周接受一次花粉挑战。在挑战前给予 TFC-007(30mg/kg,po)一次几乎完全抑制了挑战后早期和晚期鼻组织中 PGD(2)的产生。虽然预处理不影响打喷嚏和早期鼻塞的发生率,但晚期鼻塞部分但显著减轻;然而,鼻嗜酸性粒细胞浸润并未被抑制。相比之下,当 TFC-007 在挑战后 1.5 小时给予一次时,晚期反应不受影响。总之,抗原挑战后早期由 H-PGDS 产生的 PGD(2)可参与诱导晚期鼻塞,尽管其机制可能与嗜酸性粒细胞浸润无关。H-PGDS 抑制策略可能有益于过敏性鼻炎的治疗。