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Journal Abstract Search

225 related items for PubMed ID: 8388461

  • 41. [Physiological function of sigma receptors: central pharmacological effects of sigma ligands].
    Nabeshima T, Okuyama S.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 1994 Apr; 14(2):51-76. PubMed ID: 8042346
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  • 42. Interactions of sigma and phencyclidine receptor ligands with the norepinephrine uptake carrier in both rat brain and rat tail artery.
    Massamiri T, Duckles SP.
    J Pharmacol Exp Ther; 1991 Feb; 256(2):519-24. PubMed ID: 1847198
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  • 43. Synthesis and structure-activity relationships of 1-aralkyl-4-benzylpiperidine and 1-aralkyl-4-benzylpiperazine derivatives as potent sigma ligands.
    Costantino L, Gandolfi F, Sorbi C, Franchini S, Prezzavento O, Vittorio F, Ronsisvalle G, Leonardi A, Poggesi E, Brasili L.
    J Med Chem; 2005 Jan 13; 48(1):266-73. PubMed ID: 15634021
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  • 44. [3H]DTG and [3H](+)-3-PPP label pharmacologically distinct sigma binding sites in guinea pig brain membranes.
    Karbon EW, Naper K, Pontecorvo MJ.
    Eur J Pharmacol; 1991 Jan 25; 193(1):21-7. PubMed ID: 1675607
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  • 45. Multiple vascular effects of sigma and PCP ligands: inhibition of amine uptake and contractile responses.
    Massamiri T, Duckles SP.
    J Pharmacol Exp Ther; 1990 Apr 25; 253(1):124-9. PubMed ID: 2158542
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  • 46. Synthesis and pharmacological evaluation of potent and highly selective D3 receptor ligands: inhibition of cocaine-seeking behavior and the role of dopamine D3/D2 receptors.
    Campiani G, Butini S, Trotta F, Fattorusso C, Catalanotti B, Aiello F, Gemma S, Nacci V, Novellino E, Stark JA, Cagnotto A, Fumagalli E, Carnovali F, Cervo L, Mennini T.
    J Med Chem; 2003 Aug 28; 46(18):3822-39. PubMed ID: 12930145
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  • 50. [3H]BIMU-1, a 5-hydroxytryptamine3 receptor ligand in NG-108 cells, selectively labels sigma-2 binding sites in guinea pig hippocampus.
    Bonhaus DW, Loury DN, Jakeman LB, To Z, DeSouza A, Eglen RM, Wong EH.
    J Pharmacol Exp Ther; 1993 Nov 28; 267(2):961-70. PubMed ID: 8246171
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  • 52. Differential in vivo inhibition of [3H]nemonapride binding by atypical antipsychotics in rat striatum, olfactory lobes, and frontal cortex.
    Assié MB, Consul-Denjean N, Koek W, Newman-Tancredi A.
    Pharmacology; 2005 Oct 28; 75(2):63-8. PubMed ID: 16020947
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  • 53. The sigma receptor ligand (+/-)-BMY 14802 prevents methamphetamine-induced dopaminergic neurotoxicity via interactions at dopamine receptors.
    Terleckyj I, Sonsalla PK.
    J Pharmacol Exp Ther; 1994 Apr 28; 269(1):44-50. PubMed ID: 7513362
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  • 56. Sigma ligands with subnanomolar affinity and preference for the sigma 2 binding site. 1. 3-(omega-aminoalkyl)-1H-indoles.
    Perregaard J, Moltzen EK, Meier E, Sánchez C.
    J Med Chem; 1995 May 26; 38(11):1998-2008. PubMed ID: 7783131
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  • 58. Relationship between sigma-like site and progesterone-binding site of adult male rat liver microsomes.
    Yamada M, Nishigami T, Nakasho K, Nishimoto Y, Miyaji H.
    Hepatology; 1994 Nov 26; 20(5):1271-80. PubMed ID: 7927262
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  • 59. Characterization of the binding of [3H](+)-pentazocine to sigma recognition sites in guinea pig brain.
    DeHaven-Hudkins DL, Fleissner LC, Ford-Rice FY.
    Eur J Pharmacol; 1992 Dec 01; 227(4):371-8. PubMed ID: 1359973
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  • 60. BMY-14802, a sigma ligand and potential antipsychotic drug, reverses amphetamine-induced changes in neostriatal single-unit activity in freely moving rats.
    Wang Z, Haracz JL, Rebec GV.
    Synapse; 1992 Dec 01; 12(4):312-21. PubMed ID: 1361249
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