ライフサイエンスコーパス: pyrilamine

コーパス検索結果 (１語後でソート)

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1 is effect was blocked by the HRH1 antagonist pyrilamine.

2 dilatation was unaffected in the presence of pyrilamine.

3 P combined with 10 mm L-NAME plus 500 microm pyrilamine.

4 of L-NAME and the combination of L-NAME plus pyrilamine.

5 e, and the H1 histamine receptor antagonist, pyrilamine.

6 The H1 receptor antagonist pyrilamine (10 microM) blocked activation of ICl(Ca) and

7 10 microM) and blocked by the H1 antagonists pyrilamine (100 nM) or diphenhydramine (100 nM).

8 eceived substance P combined with 500 microm pyrilamine, an H1 receptor antagonist.

9 Pyrilamine, an H1R antagonist, blocked EAE, and the plat

10 of H1 and H2 histamine receptor antagonists (pyrilamine and famotidine, respectively) greatly diminis

11 The oral antihistamines pyrilamine and ranitidine were administered during toler

12 d the histamine 1 and 2 receptor antagonists pyrilamine and ranitidine, respectively, did not signifi

13 duced by histamine was inhibited by both H1 (pyrilamine) and H3 (thioperamide) but not H2 (ranitidine

14 In the H1 antagonist studies, CVC in l-NAME, pyrilamine, and combined l-NAME plus pyrilamine sites wa

15 n or celecoxib (cyclo-oxygenase inhibitors), pyrilamine, aprepitant (a neurokinin 1 receptor antagoni

16 istamine H1 antagonists, diphenhydramine and pyrilamine, at neurotensin (NT)-mediated hypothermia and

17 The histamine H(1)-receptor antagonist, pyrilamine, blocked the effects of 5 muM histamine when

18 Although the effects of pyrilamine, cromolyn, or aprepitant on ET-induced vascul

19 the much more potent histamine H1 antagonist pyrilamine did not affect antinociception mediated by NT

20 Noteworthy, the H1 receptor antagonist pyrilamine disrupted IA memory retrieval in rats, thus s

21 athing slices in medium containing 10 microM pyrilamine (H1 antagonist) blocked this stimulation-indu

22 systemically-administered antagonists of H1 (pyrilamine), H2 (zolantidine), H3 (GT-2016), or opioid (

23 Site 4 was perfused with l-NAME plus pyrilamine maleate or l-NAME plus cimetidine.

24 3 was perfused with either the H1 antagonist pyrilamine maleate or the H2 antagonist cimetidine.

25 Schild plot analysis of the effect of pyrilamine on the histamine-induced inward current revea

26 tes were significantly reduced compared with pyrilamine only sites (P < 0.05) but no significant diff

27 In vivo, treatment with antihistamines pyrilamine or cimetidine decreased lung weight and sever

28 acin), agents that interfere with histamine (pyrilamine or cromolyn), or a neurokinin antagonist (spa

29 Oral antihistamine treatments with pyrilamine or ranitidine did not impair tolerance and ne

30 inistering either an H1 receptor antagonist (pyrilamine) or an H2 receptor antagonist (cimetidine) de

31 1 receptor antagonist), or indomethacin with pyrilamine significantly reduced vascular leakage associ

32 l-NAME, pyrilamine, and combined l-NAME plus pyrilamine sites was significantly reduced compared with

33 The l-NAME and combined l-NAME plus pyrilamine sites were significantly reduced compared wit

34 en the L-NAME-only sites and the L-NAME plus pyrilamine sites.

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