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122 related items for PubMed ID: 1281498
1. Amino terminus of substance P potentiates kainic acid-induced activity in the mouse spinal cord. Larson AA, Sun X. J Neurosci; 1992 Dec; 12(12):4905-10. PubMed ID: 1281498 [Abstract] [Full Text] [Related]
2. Regulation of sigma activity by the amino-terminus of substance P in the mouse spinal cord: involvement of phencyclidine (PCP) sites not linked to N-methyl-D-aspartate (NMDA) activity. Larson AA, Sun X. Neuropharmacology; 1993 Sep; 32(9):909-17. PubMed ID: 7694172 [Abstract] [Full Text] [Related]
3. Role of the NH2-terminus of substance P in the inhibition by capsaicin of behavioral sensitization to kainic acid-induced activity in the adult mouse. Larson AA, Sun X. J Pharmacol Exp Ther; 1994 Jan; 268(1):366-71. PubMed ID: 7507995 [Abstract] [Full Text] [Related]
4. The NH2-terminus of substance P modulates NMDA-induced activity in the mouse spinal cord. Hornfeldt CS, Sun X, Larson AA. J Neurosci; 1994 May; 14(5 Pt 2):3364-9. PubMed ID: 7514216 [Abstract] [Full Text] [Related]
5. Modulation of kainic acid-induced activity in the mouse spinal cord by the amino terminus of substance P: sensitivity to opioid antagonists. Larson AA, Sun X. J Pharmacol Exp Ther; 1993 Apr; 265(1):159-65. PubMed ID: 7682611 [Abstract] [Full Text] [Related]
6. Behavioral sensitization to kainic acid and quisqualic acid in mice: comparison to NMDA and substance P responses. Sun XF, Larson AA. J Neurosci; 1991 Oct; 11(10):3111-23. PubMed ID: 1719157 [Abstract] [Full Text] [Related]
7. CP-96,345, which inhibits [3H] substance P binding, selectively inhibits the behavioral response to intrathecally administered N-methyl-D-aspartate, but not substance P, in the mouse. Velázquez RA, Kitto KF, Larson AA. J Pharmacol Exp Ther; 1997 Jun; 281(3):1231-7. PubMed ID: 9190858 [Abstract] [Full Text] [Related]
9. Is substance P a primary afferent neurotransmitter for nociceptive input? IV. 2-Amino-5-phosphonovalerate (APV) and [D-Pro2,D-Trp7,9]-substance P exert different effects on behaviors induced by intrathecal substance P, strychnine and kainic acid. Bossut D, Frenk H, Mayer DJ. Brain Res; 1988 Jul 12; 455(2):247-53. PubMed ID: 2456842 [Abstract] [Full Text] [Related]
13. An N-terminal fragment of substance P, substance P(1-7), down-regulates neurokinin-1 binding in the mouse spinal cord. Yukhananov RYu, Larson AA. Neurosci Lett; 1994 Aug 29; 178(1):163-6. PubMed ID: 7529387 [Abstract] [Full Text] [Related]
14. Cardiovascular effects of spinal cord substance P: studies with a stable receptor agonist. Keeler JR, Charlton CG, Helke CJ. J Pharmacol Exp Ther; 1985 Jun 29; 233(3):755-60. PubMed ID: 2409270 [Abstract] [Full Text] [Related]
15. Potentiation of a behavioural response in mice by spinal coadministration of substance P and excitatory amino acid agonists. Mjellem-Joly N, Lund A, Berge OG, Hole K. Neurosci Lett; 1991 Nov 25; 133(1):121-4. PubMed ID: 1724310 [Abstract] [Full Text] [Related]
17. Differential effects of substance P analogs on neurokinin 1 receptor agonists in the mouse spinal cord. Sakurada T, Yamada T, Tan-no K, Manome Y, Sakurada S, Kisara K, Ohba M. J Pharmacol Exp Ther; 1991 Oct 25; 259(1):205-10. PubMed ID: 1717679 [Abstract] [Full Text] [Related]
18. The effects of substance P analogues on the scratching, biting and licking response induced by intrathecal injection of N-methyl-D-aspartate in mice. Sakurada T, Manome Y, Tan-No K, Sakurada S, Kisara K. Br J Pharmacol; 1990 Oct 25; 101(2):307-10. PubMed ID: 1701675 [Abstract] [Full Text] [Related]