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1 infusion of methacholine chloride (Mch), an endothelium-dependent vasodilator.
2 mulative administration of acetylcholine, an endothelium-dependent vasodilator.
3 itric oxide bioavailability at rest and with endothelium-dependent vasodilators.
4 t K(IR) channels function as 'amplifiers' of endothelium-dependent vasodilators.
5 ty and preserves renal vascular responses to endothelium-dependent vasodilators.
6 at rest, during exercise, and in response to endothelium-dependent vasodilators.
7 n produced by neocortical application of the endothelium-dependent vasodilator acetylcholine (10 micr
8 r changes were determined in response to the endothelium-dependent vasodilator acetylcholine (ACh, 10
9 nses to intra-arterial administration of the endothelium-dependent vasodilator acetylcholine (P=0.03)
10 n during intracoronary administration of the endothelium-dependent vasodilator acetylcholine and the
12 threshold dose of genistein potentiated the endothelium-dependent vasodilator acetylcholine but not
19 ) were calculated during (1) infusion of the endothelium-dependent vasodilators acetylcholine (ACh) a
20 008), Responses of resistance vessels to the endothelium-dependent vasodilators acetylcholine and ADP
23 absolute forearm blood-flow responses to the endothelium-dependent vasodilator, acetylcholine, increa
24 renergic receptor agonist, phenylephrine; b) endothelium-dependent vasodilator, acetylcholine; and c)
25 ents the impaired vascular relaxation to the endothelium-dependent vasodilator ACh, this agent may be
26 ion responses of precontracted arterioles to endothelium-dependent vasodilators adenosine 5'-diphosph
27 ter 2 hours of reperfusion, but those to the endothelium-dependent vasodilator ADP and the endotheliu
28 alpha(1) -agonist) during (i) infusion of an endothelium-dependent vasodilator alone (Protocol 1: ACh
29 tudies show that apelin receptor ligands are endothelium-dependent vasodilators and potent inotropes,
30 cetylcholine (7.5, 15 and 30 microg/min), an endothelium-dependent vasodilator, and sodium nitropruss
31 in) and bradykinin (BK, 2.5 micrograms/min), endothelium-dependent vasodilators, and sodium nitroprus
34 /min), SLIGKV (160 to 800 nmol/min), and the endothelium-dependent vasodilator bradykinin (100 to 100
36 cid (LPA) has been recognized recently as an endothelium-dependent vasodilator, but several lines of
38 ate that blockade of ET-1 receptors improves endothelium-dependent vasodilator function in hypertensi
40 n of increased ET-1 activity to the impaired endothelium-dependent vasodilator function of hypertensi
41 e and that this is associated with a reduced endothelium-dependent vasodilator function, endothelium-
42 s to acetylcholine and in vitro responses to endothelium-dependent vasodilators in angiotensin II-tre
43 sepiapterin or MH4 restores the response to endothelium-dependent vasodilators in pig coronary arter
44 ctors, indicating that the reduced effect of endothelium-dependent vasodilators in those with hyperte
45 blood flow elicited by neural activity or by endothelium-dependent vasodilators in WT mice but not in
47 graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
48 graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
49 graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
50 graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
51 response to norepinephrine, and an impaired endothelium-dependent vasodilator response to acetylchol
54 t with apo A-I(M)/PC prevented impairment of endothelium-dependent vasodilator responses to acetylcho
55 on and no impairments in vasoconstrictor and endothelium-dependent vasodilator responses, associated
56 amin E therapies similarly improved arterial endothelium-dependent vasodilator responsiveness consist
57 lipoprotein levels, specific improvement in endothelium-dependent vasodilator responsiveness is simi
59 nd dilated in a dose-dependent manner to the endothelium-dependent vasodilators serotonin, ATP, and i
60 coronary artery constriction in response to endothelium-dependent vasodilator stimuli such as the co
61 w responses to intrabrachial infusion of the endothelium-dependent vasodilators substance P and acety
62 IK(Ca)/SK(Ca)), NS309 (10(-5) M), and to the endothelium-dependent vasodilators, substance P (10(-8)
65 systemic vascular reactivity in response to endothelium-dependent vasodilators, which may be mediate
66 , we hypothesized that the responsiveness to endothelium-dependent vasodilators would be greater in t