| Name | NK1 |
|---|---|
| Synonyms | BY55; CD160; CD160 antigen; CD160 antigen precursor; CD160 molecule; NK1; NK28; Natural killer cell receptor BY55… |
| Name | chloralose |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 7582497 | Chizh BA, Cumberbatch MJ, Birch PJ, Headley PM: Endogenous modulation of excitatory amino acid responsiveness by tachykinin NK1 and NK2 receptors in the rat spinal cord. Br J Pharmacol. 1995 Jul;115(6):1013-9. The effects of selective tachykinin (neurokinin, NK) NK1 and NK2 receptor antagonists have been examined on spinal neurones in alpha-chloralose anaesthetized, spinalized rats. |
85(1,1,1,5) | Details |
| 9453348 | Diz DI, Westwood B, Bosch SM, Ganten D, Ferrario C: NK1 receptor antagonist blocks angiotensin II responses in renin transgenic rat medulla oblongata. Hypertension. 1998 Jan;31(1 Pt 2):473-9. Injections of Ang II (250 fmol in 30 nL) into the nTS of chloralose-urethane anesthetized TG rats produced a significant increase in pressure of 7+/-2 mm Hg before a 13+/-3 mm Hg fall in pressure. |
3(0,0,0,3) | Details |
| 18554294 | Bongianni F, Mutolo D, Cinelli E, Pantaleo T: Neurokinin receptor modulation of respiratory activity in the rabbit. Eur J Neurosci. 2008 Jun;27(12):3233-43. Epub 2008 Jun 1. The respiratory role of neurokinin (NK) receptors was investigated in alpha-chloralose-urethane-anaesthetized, vagotomized, paralysed and artificially ventilated rabbits by using bilateral microinjections (30-50 nL) of NK receptor agonists and antagonists. We used as agonists (0.1, 0.5 and 5 mM) substance P (SP), the NK1 receptor agonists [Sar (9), Met (O2)(11)]-SP and GR 73632, the NK2 receptor agonist NKA, the NK3 receptor agonist senktide, and as antagonists (5 mM) the NK1 receptor antagonist CP-99,994 and the NK2 receptor antagonist MEN 10376. |
2(0,0,0,2) | Details |
| 7582496 | Cumberbatch MJ, Chizh BA, Headley PM: Modulation of excitatory amino acid responses by tachykinins and selective tachykinin receptor agonists in the rat spinal cord. Br J Pharmacol. 1995 Jul;115(6):1005-12. The agonists were applied by microiontophoresis in in vivo experiments in alpha-chloralose-anaesthetized, spinalized rats. 2. The NK1-selective agonist, GR 73632, enhanced responses to all three EAAs similarly, whilst the NK2-selective agonist, GR64349, reduced responses to AMPA and kainate without affecting those to and the NK3 selective agonist, senktide, enhanced responses to AMPA and kainate. 3. |
1(0,0,0,1) | Details |