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1 tion in isolated arteries and oppose certain vasorelaxants.
2 ntify new chemical spaces for KCNQ-dependent vasorelaxants.
3 interplay of endothelin-1 with the putative vasorelaxant 2-arachidonoyl glycerol, an endogenous cann
4 ), the enzyme catalyzing biosynthesis of the vasorelaxant acetylcholine (ACh), regulate vasodilation
7 ivity relationships for the antiischemic and vasorelaxant activities of KATP openers are distinct.
9 are favored in the oxygenated structure, and vasorelaxant activity is "linked" to deoxygenation, as i
13 ies as a memory aid, analgesic, spasmolytic, vasorelaxant and antihypertensive, with recent preclinic
14 support that there is no correlation between vasorelaxant and cardioprotective potencies of KATP open
19 the normal response to endothelium-dependent vasorelaxants and myocardial perfusion in response to FG
20 asma levels of adrenomedullin (AM), a potent vasorelaxant, are increased in septic shock and possibly
21 anandamide has recently been identified as a vasorelaxant but the underlying mechanisms are controver
22 mparable (ED(50) 1.7 microM) to 14,15-EET as vasorelaxants but were approximately 10-35 times less po
23 and direct intracavernosal injection of the vasorelaxant drug papaverine cause rapid increases in ph
25 The alpha-tocopherol moiety alone had no vasorelaxant effect at concentrations up to 300 micromol
28 domethacin (IM; 10 micromol/l; n = 12), this vasorelaxant effect of troglitazone was abolished (P < 0
29 er a molecular mechanism underlying rosemary vasorelaxant effects and identify new chemical spaces fo
31 r-853 were not observed, indicating that the vasorelaxant effects of cGKI are not through dephosphory
34 l dysfunction or drugs that are large-artery vasorelaxants may be effective in reducing large-artery
36 more potent, respectively, than 14,15-EET as vasorelaxants; on the other hand, their ability to block
37 of 27 results from a combination of reduced vasorelaxant potency and enhanced cardioprotective poten
38 andidate to investigate the role of residual vasorelaxant potency of 2 toward its cardioprotective ac
39 hemic myocardium is achieved by reduction of vasorelaxant potency rather than enhancement in antiisch
40 ic biological assays, displaying interesting vasorelaxant properties in rat aorta by mediating nitric
41 r designing drugs to counter the noxious and vasorelaxant properties of general anesthetics and may p
42 the hypothesis that the cardioprotective and vasorelaxant properties of K(ATP) openers follow distinc
43 tioxidant, anti-inflammatory, antitumor, and vasorelaxant properties, but possible antiarrhythmic eff
44 ike rosemary, are efficacious KCNQ-dependent vasorelaxants, quantified by myography in rat mesenteric
45 In conclusion, in cirrhotic rat livers, the vasorelaxant response to NTG is impaired owing to both a
48 l dysfunction as evidenced by blunted aortic vasorelaxant responses to acetylcholine (ACh) and calciu
52 idine alkaloid aloperine is a KCNQ-dependent vasorelaxant that potently and isoform-selectively activ