ライフサイエンスコーパス: pressor response

1 ludes attenuated blood flow and an augmented pressor response.

2 ials), and which were often accompanied by a pressor response.

3 infused mouse is a valid model for the slow pressor response.

4 e were hypotensive and exhibited a decreased pressor response.

5 Among these is a marked pressor response.

6 ly reduced expression of the naloxone-evoked pressor response.

7 blood pressure without affecting the delayed pressor response.

8 SP, 5 nmol) caused a short- and long-lasting pressor response.

9 to the pathways activated during the muscle pressor response.

10 ation of arterial pressure during the muscle pressor response.

11 nt depressor response followed by pronounced pressor response.

12 and bifurcation is excitatory and elicits a pressor response.

13 uartile range, 0-0.2), and 28% had a blunted pressor response.

14 ithout restraint in the setting of increased pressor response.

15 le afferents to the sympathetically mediated pressor response.

16 ated in the CB(1)R-evoked sympathoexcitation/pressor response.

17 tes displaying blunted slope and exaggerated pressor response.

18 riction in children with exaggerated hypoxic pressor responses.

19 g b.wt (i.v.) were effective in altering the pressor responses.

20 primary afferents that help regulate reflex pressor responses.

21 pinal cord that immediately triggered robust pressor responses.

22 ute rises in SNA was accompanied by enhanced pressor responses.

23 low catestatin predicts augmented adrenergic pressor responses.

24 kg (i.c.v.) abolished central ANG II-induced pressor responses.

25 This contraction augmented the pressor response (37+/-4 mmHg) and HR (61+/-11 bpm) with

26 One type consisted of pressor responses accompanied by bradycardia.

27 lus doses of phenylephrine evoked attenuated pressor responses after CIH (P<0.01).These data suggest

28 SNA and an initial hypotension followed by a pressor response and a longer lasting hypotensive respon

29 Stimulation of trigeminal nerve induces pressor response and improves cerebral blood flow (CBF)

30 R co-activation with hypoxia potentiates the pressor response and restricts blood flow to contracting

31 T(B2) (and presumably ET(A))-mediated portal pressor response and stellate cell constriction.

32 The [Pyr(1) ]apelin-13-mediated pressor response and the increased low frequency spectra

33 , phenylephrine induced significantly higher pressor responses and greater vasoconstrictions in the o

34 Prenatal exposure to caffeine increased pressor responses and vasoconstrictions to phenylephrine

35 ubtype 1 (VR1), inducing a neurally mediated pressor response, and (2) activation of ATP-sensitive P2

36 otentiated the magnitude and duration of the pressor response as well as the phosphatase inhibition e

37 showed a delayed rise by days 9 to 13 (slow pressor response) at the lower rates of AngII infusion.

38 bute to the blunted sympathetically mediated pressor responses, because bolus doses of phenylephrine

39 Associated with the pressor responses, c-fos expression in the cardiovascula

40 icrol) to conscious rats produced a biphasic pressor response characterized by an initial transient i

41 diaphragm fatigue development, and a blunted pressor response compared to men.

42 The exercise pressor response (DeltaMAP) did not differ between condi

43 hrine with Ang II, which restored the Ang II pressor response, did not alter the protective effects o

44 f 10 and 30 micromol/kg iv 20 attenuated the pressor responses due to the administration of exogenous

45 and an increase in TPR, followed by a brief pressor response, effects which were unaffected by SR141

46 key signaling intermediate in the transient pressor response elicited by acute injection of Ang II d

47 We show that the pressor response elicited by intra-RVLM ethanol (10 mug)

48 efferent processing of the BJR, and (2) the pressor responses elicited by alpha-methyl-5-HT were not

49 sms implicated in the sympathoexcitation and pressor responses elicited by central CB(1)R activation

50 The pressor responses elicited from the aforementioned site

51 The AngII slow pressor response enhances renal cortical O(2)(.-) and p2

52 traction and muscle stretch, but the initial pressor response evoked by static contraction was attenu

53 s for increasing MAP, and by correlating the pressor response evoked by these peptides to reported K(

54 this loss reduces the sympathoexcitatory and pressor responses evoked by RVLM stimulation.

55 A stimulation at acupoints P5-P6 reduced the pressor responses for at least 60-min.

56 site responses (viz., defensive behavior and pressor responses from the lateral column vs. quiescence

57 al artery was ligated evoked a larger reflex pressor response (i.e. exercise pressor reflex) than did

58 us system activity to activate an endogenous pressor response, improve cerebral perfusion, and decrea

59 ction following acute IHH contributes to the pressor response in addition to the established vasopres

60 tle response to cold water stress elicited a pressor response in all rats, the hemodynamic response p

61 the central CB(1)R-evoked sympathoexcitation/pressor response in conscious rats.

62 ression was associated with prolonged portal pressor response in isolated livers.

63 ective agonist [phenylephrine (PE)] caused a pressor response in KO mice, but the final arterial pres

64 travenous infusion of EGF induced an initial pressor response in rats followed by a prolonged decreas

65 vivo as demonstrated by the big ET-1-induced pressor response in rats.

66 maximally inhibited the endothelin-1-induced pressor response in rats.

67 c.v.) angiotensin (ANG) II causes a reliable pressor response in the fetus at 90% gestation.

68 and RVM, pulmonary vascular remodeling, and pressor responses in chronically hypoxic mice, suggestin

69 different effects on central ANG II-induced pressor responses in fetuses at late gestation, and that

70 n of capsaicin (0.5 mug), evoked significant pressor responses in TRPV1(+/+) and TRPV1(+/-) rats, but

71 PAT), significantly (P < 0.05) decreased the pressor response induced by intra-arterial administratio

72 The two pressor responses involve different neurochemical mechan

73 nses that are variable in rats such that the pressor response is attributable to either a large incre

74 findings demonstrate that the MK-801-induced pressor response is dependent upon the integrity of the

75 findings demonstrate that the L-NAME-induced pressor response is dependent upon the integrity of the

76 The mechanism of this pressor response is unclear.

77 tractility is enhanced to contribute to this pressor response is unknown.

78 The impact of age on exercise pressor responses is equivocal, likely because of sex-sp

79 transmitter systems through which the apelin pressor response may occur within the RVLM.

80 Because the pressor response may, in part, be caused by central nerv

81 inhibiting 50% of the Ang II-induced maximal pressor response of 25.5 mg/kg) relative to losartan.

82 nd function, which likely contributes to the pressor response of these hormones.

83 rtensive rats (SHR) respond with exaggerated pressor responses of central origin in response to pharm

84 In WKYLJ CRF specifically lowered the pressor response on trial 1 compared to control, an effe

85 ffect on seizure-induced sympathoexcitation, pressor responses, or tachycardia but abolished the prol

86 lly infused tyramine produced dose-dependent pressor responses, predicted by family history of hypert

87 the enhancement of a carbachol (CCh)-evoked pressor response produced by prior NPY administration in

88 of ATP-sensitive P2X receptors enhances the pressor response seen when muscle mechanoreceptors are e

89 ignificantly increases blood pressure with a pressor response sufficient to reduce catecholamine admi

90 ischemic handgrip exercise, despite a normal pressor response, suggests that enhanced vasoconstrictio

91 hoexcitation (p </= 0.05), and abolished the pressor responses, tachycardia, and QT interval prolonga

92 Cl produces a greater sympathoexcitatory and pressor response than infusion of hypertonic mannitol/so

93 naloxone resulted in a significantly greater pressor response than lactic acid alone, while administr

94 3, an alpha 1A/C-selective agonist, caused a pressor response that was lost in the KO and reduced but

95 atment with prazosin reversed the HS-induced pressor response to a hypotensive response (from 121 +/-

96 tivity to centrally administered AVP, and no pressor response to a peripherally injected Avpr1a-speci

97 The pressor response to acute infusion of Ang II was signifi

98 man angiotensinogen and markedly blunted the pressor response to administration of purified recombina

99 The pressor response to Ang I before and after valsartan was

100 The pressor response to Ang I was blunted significantly by v

101 the dose of ACE inhibitors was doubled, the pressor response to Ang I was no longer different from t

102 lts demonstrate that OA-NO(2) diminishes the pressor response to Ang II and inhibits AT(1)R-dependent

103 uption of the EP1 receptor blunted the acute pressor response to Ang II and reduced chronic Ang II-dr

104 Deletion of p47phox attenuated the pressor response to Ang II; however, coinfusion of pheny

105 s and that AT2 receptors do not modulate the pressor response to AngII.

106 level of ACE inhibition was assessed by the pressor response to angiotensin (Ang) I in patients who

107 portantly, 7 days after virus infection, the pressor response to angiotensin (Ang) II (200 pmol intra

108 n I (AI) was measured and normalized for the pressor response to angiotensin II (AII) to assess inhib

109 xpression by C1 neurons is essential for the pressor response to angiotensin II and that this pathway

110 tly elevated in the transgenic mice, but the pressor response to angiotensin II was augmented.

111 The pressor response to ascending doses of Ang I was evaluat

112 for recording blood pressure, modulated the pressor response to aversive stress.

113 this pathway plays an important role in the pressor response to aversive stress.

114 , an ASIC agonist, but did not attenuate the pressor response to capsaicin, a TRPV1 agonist.

115 nses to lactic acid, but also attenuated the pressor response to capsaicin.

116 cies with respect to causing the exaggerated pressor response to contraction seen in rats with ligate

117 In the six ligated rats, however, the pressor response to contraction was attenuated by L16198

118 ited by N-nitro-L-arginine methyl ester, the pressor response to dexfenfluramine is greatly enhanced.

119 le autonomic traits: baroreflex function and pressor response to environmental stress.

120 Similarly, the pressor response to EP1-selective agonists sulprostone a

121 There was a significant increase in the peak pressor response to ET (10 microg/kg intravenously) in p

122 The pressor response to ET in vitro was significantly enhanc

123 The pressor response to ET-1 was determined in vitro using i

124 The pressor response to exogenous angiotensin I (AI) was mea

125 tential for a counteracting, anti-dipsogenic pressor response to hindbrain AngII allows for lingering

126 mg/kg, i.c.v.) showed a potentiation of the pressor response to i.c.v. ANG II, accompanied by bradyc

127 plasma prostacyclin levels and a significant pressor response to indomethacin in PHT animals.

128 ot in platelets and exhibited an exaggerated pressor response to infused iPF(2alpha)-III compared wit

129 Agtr1a -/-Agtr1b -/- mice have no systemic pressor response to infusions of angiotensin II, but the

130 We tested the hypothesis that the pressor response to inspiratory work would be similar be

131 The pressor response to intravenous injection of Big endothe

132 The rapid, systemic pressor response to intravenous LTC4 was also diminished

133 Changes in platelet 5-HT uptake and the pressor response to intravenous tyramine were assessed f

134 By contrast, both the pressor response to iPF(2alpha)-III and its effects on p

135 ked the diazepam-induced potentiation of the pressor response to isoguvacine.

136 f raise training of the dominant limb on the pressor response to isometric exercise of the triceps su

137 unted both the increase in plasma NE and the pressor response to L-DOPS in all patients

138 amiloride and APETx2 greatly attenuated the pressor response to lactic acid, an ASIC agonist, but di

139 sure response to right handgrip, whereas the pressor response to left handgrip did not change.

140 subjects, unlike MSA subjects, although the pressor response to mental arithmetic was reduced.

141 cle afferents, serves to regulate the reflex pressor response to metabolic stimuli.

142 R-floxed mice enabled demonstration that the pressor response to microinjection of angiotensin II int

143 receptors at the dorsal horn level blunt the pressor response to muscle activity.

144 ion by alpha,beta-methylene ATP enhanced the pressor response to muscle stretch by 42% in control ani

145 At 6 hrs, there was an attenuated pressor response to norepinephrine (p < .01) despite blo

146 In vivo, the pressor response to norepinephrine was markedly reduced

147 The pressor response to norepinephrine was reduced following

148 le, this strain responds with an exaggerated pressor response to pharmacological stimulation of centr

149 e afferents and the baroreflex evoked by the pressor response to phenylephrine (3-25 microg kg(-1), i

150 The slow pressor response to prolonged infusions of angiotensin I

151 lated hypertension; they also show a reduced pressor response to salt loading.

152 The pressor response to static muscle contraction and alpha,

153 in animals, ruling out an effect of enhanced pressor response to stress following prenatal protein re

154 n-treated and DCM rats displayed a decreased pressor response to the intra-arterial administration of

155 The pressor response to tyramine differentially distinguishe

156 e higher dose would differentially blunt the pressor response to tyramine, a marker for NE uptake.

157 Thus, we hypothesized that the pressor response to VR1 stimulation would be smaller and

158 phragm strength, women and men had a similar pressor response to work-matched inspiratory loading, in

159 In MSA patients, the pressor response to yohimbine and the decrease in SBP wi

160 er, LPA(6) KO mice also displayed attenuated pressor responses to an adrenergic agent and abnormal bl

161 The present results suggest that pressor responses to AngII are mediated by the activatio

162 Pressor responses to AngII were attenuated by candesarta

163 hibit significant hypertension and increased pressor responses to angiotensin II and endothelin-1; th

164 asal blood pressure was similar, however the pressor responses to both acute and chronic angiotensin

165 RPC6 decreased the renal sympathetic and the pressor responses to both contraction and stretch, the l

166 For example, the peak pressor responses to contraction in TRPV1(+/+) , TRPV1(+

167 pressure, findings which indicated that the pressor responses to contraction were not caused by elec

168 he sympathoexcitatory (splanchnic nerve) and pressor responses to electrical stimulation of the RVLM

169 decreased vascular resistance, and elevated pressor responses to environmental (cold) stress.

170 Systemic pressor responses to ET-1 and angiotensin II were simila

171 pulmonary vascular resistance and pulmonary pressor responses to ET-1, angiotensin II, and hypoxia;

172 hronically block or, for L-164,282, to spare pressor responses to exogenous Ang II.

173 ermittent contraction but did not reduce the pressor responses to femoral arterial injection of compo

174 Importantly, AV3V lesions attenuated pressor responses to increasing doses of 5-HT (3 +/- 1,

175 In anesthetized rats, the pressor responses to increasing doses of norepinephrine

176 Pressor responses to increasing doses of phenylephrine a

177 echanical stimulus, but had no effect on the pressor responses to intra-arterial injection of alpha,b

178 In summary, pressor responses to intravenous 5-HT are diminished by

179 Pressor responses to intravenous norepinephrine, vasopre

180 t, the high dose of amiloride attenuated the pressor responses to lactic acid, but also attenuated th

181 ypovolaemia, where they may rely on systemic pressor responses to maintain perfusion of posterior bra

182 The tendency to show exaggerated pressor responses to mental stress is a significant inde

183 l laminae of the dorsal horn potentiates the pressor responses to microinjection of L-glutamate.

184 Pressor responses to norepinephrine and PNU-37883A (a va

185 mals transfected with the eNOS gene, whereas pressor responses to norepinephrine and U46619 were not

186 047 injection attenuates the sympathetic and pressor responses to passive muscle stretch in decerebra

187 mpathetic nerve activity (~70%), and blunted pressor responses to phenylephrine and angiotensin II.

188 renal sodium excretion or volume expansion; pressor responses to phenylephrine were enhanced and bar

189 The tendency to show exaggerated pressor responses to psychological demands may be a sign

190 Both TRPC6 antagonists decreased the reflex pressor responses to static contraction (-32 to -42%; P

191 Pressor responses to static handgrip were also attenuate

192 od too rapidly for accurate measurement, and pressor responses to the injection of drug were greatly

193 The initial pressor response was also attenuated by pretreatment wit

194 A blunted pressor response was associated with a nearly 2-fold mor

195 The pressor response was not antagonized by prior injection

196 lity to suppress BMI-induced tachycardic and pressor responses was additive.

197 The late, but not the early pressor response, was prevented by pretreatment with chl

198 Both pressor responses were abolished by i.c.v. pretreatment

199 These pressor responses were accompanied by a significant tach

200 Higher mental stress pressor responses were associated with more constriction

201 The chemoreflex sympathoexcitatory pressor responses were attenuated by an acute systemic a

202 Pressor responses were elicited by microinjections of l-

203 Central ANG II-induced fetal pressor responses were not altered by PD123319 (0.8 mg/k

204 Rs in C1 neurons induced a greater sustained pressor response when compared to the control viral-inje

205 N) in conscious unrestrained mice elicited a pressor response, which was abolished by ICV preinjectio

206 In rats, intravenous 16a blocks big ET pressor responses with 30-fold greater potency than 1.

207 Another type consisted of pressor responses without any change in heart rate; such