Publications in Chronological Order and Hot Links:

Cumbay, M.G.and Watts, V.J. "Novel regulatory properties of human type 9 adenylate cyclase (AC9)" J. Pharmacol. Exp. Ther.310: 108-115, 2004
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Bradley, K.C., Mullins, A.J., Meisel, R.L. and Watts, V.J. "Sexual experience alters D1 receptor mediated cyclic AMP production in the nucleus accumbens of female syrian hamsters" Synapse 53:20-27, 2004.
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Johnston, C.A., Beazely, M.A., Bilodeau, M.L., Andrisani, O., and Watts, V.J. " Differentiation-induced alterations in cyclic AMP signaling in the Cath.a differentiated (CAD) neuronal cell line." J. Neurochem. 88:1497-1508, 2004.
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Jarrahian, A, Watts, V.J., and Barker, E.L. "D2 dopamine receptors modulate Ga-subunit coupling of the CB1 cannabinoid receptor" J. Pharmacol. Exp. Ther.308:880-886, 2004
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Vortherms, T.A. and Watts, V.J.Sensitization of neuronal A2A adenosine receptors following persistent D2 dopamine receptor activation" J. Pharmacol. Exp. Ther.308:221-227, 2004
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Lisinicchia, J.G., and Watts, V.J. "Sensitization of adenylate cyclase by short-term activation of 5-HT1A receptors" Cell. Signal. 15:1111-1117, 2003.
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Johnston, C.A., and Watts, V.J. "Sensitization of adenylate cyclase: A general mechanism of neuroadaptation to persistent activation of Gi/o-coupled receptors?" Life Sci. 73:2913-2925, 2003.
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Kurrasch-Orbaugh, D., Parrish, J.C., Watts, V.J., and Nichols D.E "A Complex Signaling Cascade Links the Serotonin2A Receptor to Phospholipase A2 Activation: The Involvement of MAP Kinases" J. Neurochem. . 86: 980-991, 2003.
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Kurrasch-Orbaugh, D., Barker, E.L., Watts, V.J., and Nichols D.E "Serotonin 5-hydroxytryptamine 2A receptor-coupled phospholipase C and phospholipase A2 signaling pathways have different receptor reserves " J. Pharmacol. Exp. Therap. 304:229-237, 2003.
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Johnston, C.A., Beazely,M.A., Vancura, A.F., Wang, J.K.T., and Watts, V.J. "Heterologous sensitization of adenylate cyclase is PKA-dependent in CAD-D2L cells" J. Neurochem. . 82: 1087-96, 2002.
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Watts, V.J "Molecular mechanisms for heterologous sensitization of adenylate cyclase". J. Pharmacol. Exp. Ther. 302:1-7, 2002.
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Watts, V.J., Taussig, R., Neve, R.L., and Neve, K.A. "Dopamine D2 receptor-induced heterologous sensitization of adenylyl cyclase requires Gs: characterization of Gs-insensitive mutants of adenylyl cyclase V ". Mol. Pharmacol. . 60:1168-1172, 2001.
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Neve, K.A., Cumbay, M.G., Thompson, K.R., Yang, R. Buck, D.C., Watts,V.J., DuRand, C.J., and Teeter, M.M. "Modeling and mutational analysis of a putative sodium-binding pocket on the dopamine D2 receptor". Mol. Pharmacol. 60:373-381, 2001.
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Johnston, C.A., Cumbay, M.G., Vortherms, T.A., and Watts,V.J. "Sensitization of adenylate cyclase in NS20Y-D2L cells by adrenoceptor activation of dopamine D2 receptors". FEBS Lett 497:85-89, 2001.
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Cumbay, M.G. and Watts,V.J."Heterologous sensitization of recombinant adenylate cyclases by activation of D2 dopamine receptors". J. Pharmacol. Exp. Ther. 297:1201-1209, 2001.
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Schutzer, W.E., Watts, V.J., Chapman, J. Cumbay, M.G., Neve, K.A., Neve, R.L., and Mader, S.L. "Viral-mediated gene delivery of constitutively activated Gs alters vasoreactivity". Clin. and Exp. Pharmacol. and Physio. 27:9-13, 2000.
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Blair, J.B., Kurrasch-Orbaugh, D., Marona-Lewicka, D., Cumbay, M.G., Watts, V.J., Barker, E.L. and Nichols, D.E. "Effect of ring flourination on the pharmacology of hallucinogenic tryptamines". J. Med. Chem. 43:4701-4710, 2000.
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Chapman, J. Schutzer, W.E., Watts, V.J., and Mader, S.L. "Impaired cholera toxin relaxation with age in rat aorta". J. Gerontol. 54:B154-B159, 1999.
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Watts, V.J., Vu, M.N., Wiens, B.L., Jovanovic, V., Van Tol, H.H.M. and Neve, K.A. "Short- and long-term heterologous sensitization of adenylate cyclase by D4 dopamine receptors". Psychopharmacology 141:83-92, 1999.
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Watts, V.J., Wiens, B.L., Cumbay, M.G., Vu, M.N., Neve, R.L., and Neve, K.A. "Selective Activation of Go by D2L Dopamine Receptors in NS20Y Neuroblastoma Cells". J. Neuroscience 18: 8692-8699, 1998.
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Lewis, M.M., Watts, V.J., Lawler, C.P., Nichols, D.E. and Mailman, R.B. "Homologous desensitization of the D1A dopamine receptor: Efficacy in causing desensitization dissociates from both receptor occupancy and functional potency". J. Pharmacol. Exp. Ther. 286:345-353, 1998.
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Watts, V.J. and Neve, K.A. "Activation of type II adenylate cyclase by D2 and D4 but not D3 dopamine receptors". Mol. Pharmacol.. 52:181-186, 1997.
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Watts, V.J. and Neve, K.A. "Sensitization of endogenous and recombinant adenylate cyclase by activation of D2 dopamine receptors". Mol. Pharmacol.. 50: 966-976, 1996.
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Negash, K., Nichols, D.E., Watts, V.J., and Mailman, R.B. "Further definition of the D1 dopamine receptor pharmacophore: Synthesis of trans-6,6a,7,8,9,13b-hexahydro-5H-benzo[d]azepeines as rigid analogues of ß-phenyldopamine". J. Med. Chem. 40:2140-2147, 1997.
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Ghosh, D. Snyder, S.E., Watts, V.J., Mailman, R.B., and Nichols, D.E. "8,9-Dihydoxy--2,3,7,11b tetra hydro-1H-naph[1,2,3-de] isoquinolone: a potent full dopamine D1 agonist containing a rigid ß-phenyl dopamine pharmacophore". J. Med. Chem. 39:549-555, 1996.
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Mottola, D.M., Leiter, S., Tropsha, A., Watts, V.J., Wyrick, S.D., Nichols, D.E., and Mailman, R.B. "Conformational analysis of D1 dopamine receptor agonists: pharmacophore assessment and receptor mapping". J. Med. Chem. 39:285-296, 1996.
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Watts, V.J., Lawler, C.P., Gonzales, A.J., Zhou, Q-Y., Civelli, O., Nichols, D.E., and Mailman, R.B. "Spare receptors and intrinsic activity: studies with D1 dopamine receptor agonists: the role of spare receptors". Synapse 21: 177-187, 1995.
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Lawler, C.P., Gilmore, J.H., Watts, V.J., Walker, Q.D., Southerland, W.B., Cook, L.L., Mathis, C.A., and Mailman, R.B. "Interhemispheric modulation of dopamine receptor subtypes interactions in the unilateral 6-OHDA rodent model". Synapse 21:299-311, 1995.
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Watts, V.J., Lawler, C.P., Neve, K.A., Nichols, D.E., and Mailman, R.B. "LSD and structural analogs: pharmacological evaluation at D1 dopamine receptors". Psychopharmacology 118:401-409, 1995.
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Gilmore, J.H., Watts, V.J., Lawler, C.P., Nichols, D.E., and Mailman, R.B. "“Full” dopamine D1 agonists in human caudate: biochemical properties and therapeutic implications". Neuropharmacology 34:481-488, 1995.
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Paterson, A., Boyer, J.L., Watts, V.J., Morris, A.J., Price, E.M., and Harden, T.K. "Concentration of enzyme dependent activation of PLC-ß1 and PLC -b2 by Ga11 and bg subunits". Cell. Signal. 7:709-720, 1995.
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Knoerzer, T.A., Watts, V.J., Nichols, D.E., and Mailman, R.B. "Dopaminergic benzo[a]phenanthridines: resolution and pharmacological evaluation of the enantiomers of dihydrexidine, the full efficacy D1 dopamine receptor agonist.". J. Med. Chem. 38:3062-3070, 1995.
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Snyder, S.E., Aviles-Garay, F.A., Chakraborti, R., Nichols, D.E., Watts, V.J., and Mailman, R.B. "Synthesis and evaluation of 6,7-dihydroxy-2,3,4,8,9,13b-hexahydro-lH-benzo[6,7]cyclohepta[1,2,3-ef][3]benzazepine, 6,7-dihydroxy-1,2,3,4,8,l2b-hexahydroanthr[10.4a,4-cd]azepine, and 10 aminomethyl-9,10-dihydro-1,2-dihydroxyanthracene as conformationally restricted analogues of b-phenyldopamine". J. Med. Chem. 38:2395-2409, 1995.
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Brewster, W.K., Nichols, D.E., Watts, V.J., Riggs, R.M., Mottola, D.M., and Mailman, R.B. "Evaluation of Cis- and Trans-9- and 11-Hydroxy­-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridines as structurally rigid, selective D1 dopamine receptor ligands". J. Med. Chem. 38:318-327, 1995.
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Minor, D.L., Wyrick, S.D., Charifson, P.S., Watts, V.J., Nichols, D.E., and Mailman, R.B. "Synthesis and molecular modeling of l-phenyl-1,2,3,4-tetrahydroisoquinolines and related 5,6,8,9-tetrahydro-13bH-dibenzo[a]quinolizines as D1 dopamine antagonists". J. Med. Chem. 37:4317-4328, 1994.
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Knoerzer, T.A., Nichols, D.E., Brewster, W.K., Watts, V.J., Mottola, D.M., and Mailman, R.B. "Dopaminergic benzo[a]phenanthridines: resolution and pharmacological evaluation of the enantiomers of dihydrexidine, the full efficacy D1 dopamine receptor agonist". J. Med. Chem. 37:2453-2460, 1994.
Medline Abstract

Negash, K., Nichols, D.E., Watts, V.J., and Mailman, R.B."Synthesis of l-phenyl-2-amino-1,2,3,4-tetrahydronapthalene derivatives with dopamine D2 receptor affinity". Med. Chem. Res 5:33-42, 1994.

Watts, V.J., Lawler, C.P., Gilmore, J.H., Southerland, S.B., Nichols, D.E., and Mailman, R.B. "Dopamine D1 receptors: efficacy of full (dihydrexidine) vs. partial (SKF38393) agonists in primates vs. rodents". Eur. J. Pharmacol 242:165-172, 1993.
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Watts, V.J., Lawler, C.P., Knoerzer, T., Mayleben, M.A., Neve, K.A., Nichols, D.E., and Mailman, R.B."Hexahydrobenzo[a]phenanthridines: Novel ligands for D3 dopamine receptors". Eur. J. Pharmacol. 239:271-273, 1993.
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Lysle, D.T., Coussons, M.E., Watts, V.J., Bennett, E.H., and Dykstra, L.A. "Morphine-induced alterations of immune status: dose-dependency, compartment specificity, and antagonism by naltrexone". J. Pharamcol. Exp. Ther. 265:1071-1078, 1993.
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Lysle, D.T., Coussons, M.E., Watts, V.J., Bennett, E.H., and Dykstra, L.A. "Morphine-induced modulation of immune status: evidence for opioid receptor mediation and compartment specificity". Adv. Exp. Bio. Med. 335:53-59, 1993.
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Faulkner, T.P., Cantleberry, S.G., Watts, V.J., and Hussain, A.S. "Comparative pharmacokinetics of ethanol in inbred strains of mice using doses based on total body water". Alcoholism: Clin. Exp. Res. 14:82-86, 1990.
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