ライフサイエンスコーパス: alpha2 agonist

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1 inephrine (NE), clonidine (CLON, a selective alpha2-agonist) and phenylephrine (PE, a selective alpha

2 fect profiles when compared with traditional alpha2 agonists, and may thereby allow for more widespre

3 Besides alpha2-agonists, apical uptake was inhibited by verapami

4 ing the response to intravenous injection of alpha2-agonist before and after the infusion.

5 ttens received microinfusions (1 mul) of the alpha2 agonist clonidine (CLON; 1.32 nmol), and half rec

6 ,N-MePhe4, Gly-ol5]enkephalin (DAMGO) or the alpha2 agonist clonidine inhibited voltage-gated Ca2+ cu

7 of the alpha1-agonist phenylephrine and the alpha2-agonist clonidine.

8 cocaine CPP in the presence and absence of a alpha2-agonist (clonidine), beta-adrenergic receptor ant

9 The alpha2-agonist, clonidine, had a weak effect in LSI neur

10 eatment of HUVECs, but not neutrophils, with alpha2-agonists decreased transendothelial migration, wi

11 The nonsubtype-selective alpha2 agonist dexmedetomidine completely blocked the co

12 both norepinephrine and the highly selective alpha2 agonist dexmedetomidine each reversed the VLPO de

13 to investigate the role of the alpha2aAR in alpha2 agonist-evoked analgesia and adrenergic-opioid sy

14 ernal cesium and external barium, opioid and alpha2 agonists had no effect at potentials more negativ

15 Alpha2 agonists have been in clinical use for decades, p

16 In recent years, alpha2 agonists have found wider application, particular

17 alpha2 agonists have similar potencies in stimulating Sr

18 nhibition of vas deferens contraction by the alpha2 agonist in alpha2A-AR knockout mice was only 42 +

19 phrine (an alpha1 agonist) and clonidine (an alpha2 agonist) in 10 healthy men during rhythmic handgr

20 To put the alpha2-agonists into clinical context, we will discuss t

21 ission at IPL and that brimonidine and other alpha2 agonists may protect RGCs under disease condition

22 The mutation also decreased alpha2-agonist-mediated spinal analgesia and blocked the

23 y before naloxone with clonidine (20 microg; alpha2 agonist), MK-801 (3 microg; noncompetitive NMDA a

24 Interestingly, alpha2-agonists prevented the TNF-alpha-mediated decreas

25 Guanabenz, an alpha2-agonist, prolonged baseline expiration and potent

26 alpha2 Agonists, such as brimonidine, have been shown to

27 neuroprotection of retinal ganglion cells by alpha2 agonists, such as brimonidine, in animal models o

28 Compelling evidence suggests that alpha2 agonists, such as brimonidine, protect retinal ga

29 The alpha2 agonists that are currently employed in anesthesi

30 ther in murine nor in human neutrophils upon alpha2-agonist treatment.

31 he NE-induced inhibition was mimicked by the alpha2-agonist, UK14,304, but not by the alpha1- or beta

32 (P < 0.05) and sensitivity (P < 0.05) to the alpha2 agonist UK14304 was lower in protein-, but not in

33 The hypotensive effect of alpha2 agonists was completely absent in alpha2A-deficie

34 eir hypnotic response to dexmedetomidine (an alpha2 agonist) was determined.

35 phrine (alpha1-agonist) and dexmedetomidine (alpha2-agonist) were assessed.

36 henylephrine (alpha1-agonist) and clonidine (alpha2-agonist) were assessed.

37 e (selective alpha1-agonist), and clonidine (alpha2-agonist) were determined in 10 young (aged 26+/-1

38 fter we will compare and contrast the use of alpha2-agonists with clinically available agents, and sp

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