ライフサイエンスコーパス: myogenic tone

1 Ca2+ free) to 116 +/- 7 micron or by 45 % ('myogenic tone').

2 numerous physiological processes, including myogenic tone.

3 ations of XE991 enhance mesenteric and renal myogenic tone.

4 ls, other ion channel proteins that modulate myogenic tone.

5 ansgenic mice exhibited a robust increase in myogenic tone.

6 ks and waves but increased global Ca(2+) and myogenic tone.

7 diabetic pigs developed comparable levels of myogenic tone.

8 (2)S production, depolarize VSM, and enhance myogenic tone.

9 ne expression of each subunit, which reduced myogenic tone.

10 ity, synaptic transmission and regulation of myogenic tone.

11 anism in the regulation of resistance artery myogenic tone.

12 elevated arterial [Ca(2+)](i), and enhanced myogenic tone.

13 ntracellular calcium ([Ca2+]i) and decreased myogenic tone.

14 a2(+/-), but not alpha1(+/-), have increased myogenic tone.

15 ood pressure reflect the in vitro changes in myogenic tone.

16 Regulation of the microcirculation includes myogenic tone.

17 nels play an essential role in regulation of myogenic tone.

18 effect on blood glucose or resistance artery myogenic tone.

19 o 80 mmHg and allowed to develop spontaneous myogenic tone.

20 l volume, electrical activity and, possibly, myogenic tone.

21 l arterioles resulting in the development of myogenic tone (28% from maximum dilatation).

22 ng MR in SMCs (SMC-MR) have reduced vascular myogenic tone, agonist-dependent contraction and express

23 he AT1 R blocker losartan (1 mum) diminished myogenic tone and blocked stretch-induced cation current

24 and latrunculin) inhibit the development of myogenic tone and decrease the effectiveness of myogenic

25 Inhibiting CSE also enhanced myogenic tone and depolarized VSM in sham but not IH art

26 man and porcine retinal arterioles developed myogenic tone and dilated dose dependently to bradykinin

27 bligatory role in force development, both in myogenic tone and during alpha1-adrenoceptor activation.

28 kinase (ROCK) inhibitor H-1152 blocked both myogenic tone and endothelin-1-induced constriction.

29 Conversely, ROCK activation mediates myogenic tone and endothelin-1-induced vasoconstriction.

30 hese data suggest that streptomycin inhibits myogenic tone and K+-induced isometric force largely by

31 /-) or chronic ouabain) apparently regulates myogenic tone and long-term blood pressure whereas reduc

32 ocin on cerebral artery (250 to 300 microns) myogenic tone and on vasodilations to the synthetic KATP

33 age-matched control rats were evaluated for myogenic tone and reactivity.

34 Baseline myogenic tone and resting membrane potential were not af

35 Both myogenic tone and the pressure- and temperature-dependen

36 e several physiological processes, including myogenic tone and thus, artery diameter.

37 nhibited pressure-induced vasoconstriction ("myogenic tone"), and attenuated pregabalin-induced vasod

38 on, leading to an increase in both pressure (myogenic tone)- and depolarization-induced vasoconstrict

39 ees C, arteries developed pressure-dependent myogenic tone, and this was associated with a pressure-d

40 tion in mediating the HF-induced increase in myogenic tone are two further findings: a blunting of pa

41 Myogenic tone, assessed as the difference between intern

42 TRPP2 knockdown did not alter myogenic tone at 20 mmHg but reduced tone between approx

43 HFD/STZ treatment induced a progressive myogenic tone augmentation in mesenteric and olfactory c

44 alcohol exposure did not affect spontaneous myogenic tone, but enhanced the dilator response of pene

45 icted pressurized (to 60 mmHg) arteries with myogenic tone by 44 micron (approximately 22 %).

46 permeability, responses to oxidative stress, myogenic tone, cellular proliferative activity, and ther

47 Arteries from diabetic rats showed decreased myogenic tone compared with control arteries, and this d

48 n-dependent inhibition of pressure-dependent myogenic tone consistent with previous reports of mechan

49 d from patients with diabetes have augmented myogenic tone, despite reasonable blood glucose control.

50 Myogenic tone developed at an intraluminal pressure of 3

51 e, BK beta1 allows the BK channels to reduce myogenic tone, facilitating vasodilation.

52 tation of saphenous vein, with its intrinsic myogenic tone, from the low-pressure, minimally pulsatil

53 Only the NCX blockers normalize the elevated myogenic tone in alpha2(+/-) arteries because this tone

54 ) attenuated Ca(2+) waves, global Ca(2+) and myogenic tone in arteries and arterioles but had no effe

55 Iberiotoxin enhanced myogenic tone in both groups but more in sham than IH.

56 n the SR of arterial smooth muscle regulates myogenic tone in cerebral arteries solely through activa

57 a blunting of paxilline-induced increase in myogenic tone in HF mice compared to controls (0.9 vs. 1

58 erfering RNA targeting RGS5 caused augmented myogenic tone in intact mesenteric arteries and increase

59 ilatory responses to an NO donor and loss of myogenic tone in KW animals were also rescued with Nox1

60 CX blockers (SEA0400 and KB-R7943) normalize myogenic tone in ouabain-treated arteries.

61 inactivation or scavenging of H(2)S enhanced myogenic tone in sham arteries to the level of IH.

62 ses endothelial H(2)S production to increase myogenic tone in small mesenteric arteries.

63 iotensin II as a neurohumoral signal for the myogenic tone in the internal anal sphincter.

64 bserved a similar contribution of 20-HETE to myogenic tone in the mesenteric microvasculature.

65 el activity, thus providing tight control of myogenic tone in the microcirculation.

66 are likely to play a key role in regulating myogenic tone in vascular tissue.

67 rteries at low intravascular pressure, where myogenic tone is absent.

68 Coronary myogenic tone is dependent on ERK1/2 and decreased after

69 We conclude that myogenic tone is not significantly different in pregnant

70 Although pressure-induced constriction ("myogenic tone") is a major contributor to the regulation

71 in two indirect assays of Na+ pump function: myogenic tone (MT) in isolated, pressurized rat mesenter

72 EGFR transactivation under pressure-induced myogenic tone (MT).

73 y), and that HF does not alter the increased myogenic tone of BK beta1-null mice.

74 Myogenic tone of coronary arterioles was measured by vid

75 ion- and endothelium-dependent effect on the myogenic tone of rat ophthalmic artery.

76 systolic HF post-myocardial infarction, the myogenic tone of third-order mesenteric resistance vesse

77 sure causes depolarization and constriction (myogenic tone) of small arteries and arterioles, and thi

78 LRRC26 knockdown also increased myogenic tone over a range (40-100 mm Hg) of intravascul

79 -kappaB inhibitors had significantly reduced myogenic tone potentiation and improved EDR.

80 (Ca) channels and vasodilation, reducing the myogenic tone that underpins tissue blood-flow autoregul

81 pendent dilation of pressurized vessels with myogenic tone that was accompanied by a corresponding de

82 In the control condition of myogenic tone the arteries were constricted to 62 % (n =

83 ooth muscle cell TNF drives the elevation of myogenic tone via enhanced sphingosine-1-phosphate (S1P)

84 Myogenic tone was abolished by 2 microM nimodipine, but

85 Myogenic tone was assessed over a range of intraluminal

86 Myogenic tone was decreased in coronary microvessels aft

87 Myogenic tone was enhanced by 25 mM, but decreased by 40

88 However, we found that development of myogenic tone was greater in arteries from AT1 Ra knocko

89 Myogenic tone was greater in mesenteric arteries from IH

90 Pressure-induced myogenic tone was increased in MRA and coronary artery f

91 2+) event frequency was inhibited, and basal myogenic tone was increased, by either RN1734 or TRAM-34

92 Myogenic tone was reduced in coronary arterioles post-C/

93 Pressure-induced myogenic tone was significantly potentiated, while endot

94 Myogenic tone was unchanged, but over a range of transmu

95 Pressure-induced constrictions ("myogenic tone") were greater (approximately 2-fold) in i

96 depolarization and constriction to pressure (myogenic tone) were blunted in PAs from TgNotch3(R169C)

97 osterior cerebral arteries display augmented myogenic tone, which can be fully reversed in vitro by t