S. Matta

发表

Protection Genes in Nucleus Accumbens Shell Affect Vulnerability to Nicotine Self-Administration across Isogenic Strains of Adolescent Rat

S. Gong, Rui Luo, Hao Chen, 2014, PloS one.

Lentiviral-mediated knock-down of GD3 synthase protects against MPTP-induced motor deficits and neurodegeneration

D. Heck, M. P. McDonald, G. Fan, 2019, Neuroscience Letters.

Self-administration in rats allowed unlimited access to nicotine

S. Matta, B. Sharp, J. Valentine, 1997, Psychopharmacology.

Genotype-dependent effects of adolescent nicotine exposure on dopamine functional dynamics in the nucleus accumbens shell in male and female mice: a potential mechanism underlying the gateway effect of nicotine

E. Chesler, C. Blaha, G. Mittleman, 2011, Psychopharmacology.

Decreased Firing Rates and Altered Firing Patterns Drug-Related Dyskinesias in Parkinson's Disease: Internal Pallidal Neuronal Activity During Mild

P. Starr, L. Metman, S. Shimamoto, 2007 .

Gestational Nicotine Exposure Attenuates Nicotine-Stimulated Dopamine Release in the Nucleus Accumbens Shell of Adolescent Lewis Rats

Yitong Fu, S. Matta, B. Sharp, 2004, Journal of Pharmacology and Experimental Therapeutics.

Fostering itself increases nicotine self-administration in young adult male rats

Hao Chen, S. Matta, B. Sharp, 2013, Psychopharmacology.

Rat strain differences in nicotine self-administration using an unlimited access paradigm

S. Matta, B. Sharp, Yitong Fu, 2002, Brain Research.

Nicotine activates NPY and catecholaminergic neurons in brainstem regions involved in ACTH secretion

S. Matta, B. Sharp, J. Valentine, 1997, Brain Research.

Detection by in vivo microdialysis of nicotine-induced norepinephrine secretion from the hypothalamic paraventricular nucleus of freely moving rats: dose-dependency and desensitization.

S. Matta, B. Sharp, 1993, Endocrinology.

S. L. Parker, S. Matta, B. Sharp, 2022 .

Nicotine administration enhances NPY expression in the rat hypothalamus

Ming D. Li, S. L. Parker, S. Matta, 2000, Brain Research.

Prenatal alcohol exposure (PAE) reduces the size of the forepaw representation in forepaw barrel subfield (FBS) cortex in neonatal rats: relationship between periphery and central representation

R. S. Waters, Cheng X. Li, A. Elberger, 2006, Experimental Brain Research.

Genome-Wide Gene Expression Profiling of Nucleus Accumbens Neurons Projecting to Ventral Pallidum Using both Microarray and Transcriptome Sequencing

Robert W. Williams, S. Gong, W. Taylor, 2011, Front. Neurosci..

The brain-immune axis and drugs of abuse

D. Saphier, S. Matta, 1996, Journal of Neuroimmunology.

Social Interaction Promotes Nicotine Self-Administration with Olfactogustatory Cues in Adolescent Rats

Hao Chen, S. Matta, B. Sharp, 2011, Neuropsychopharmacology.

Nicotine regulates nicotinic cholinergic receptors and subunit mRNAs in PC 12 cells through protein kinase A.

S. Matta, B. Sharp, T. Madhok, 1995, Brain research. Molecular brain research.

Tumor Necrosis Factor-α is a Potent ACTH Secretagogue: Comparison to Interleukin-1β

P. Peterson, C. Chao, S. Matta, 1989 .

Channel Subunit in Brain Alternatively Spliced Isoforms of the Kv3.1 Potassium Differential Subcellular Localization of the Two

Mark Ellisman, B. Rudy, F. Zhou, 2015 .

Norepinephrine release in amygdala of rats during chronic nicotine self-administration: an in vivo microdialysis study

S. Matta, B. Sharp, Victoria B Kane, 2003, Neuropharmacology.

Response of the hypothalamo-pituitary-adrenal axis to nicotine

S. Matta, B. Sharp, J. Valentine, 1998, Psychoneuroendocrinology.

Pancreatic Islet Cell Reaggregation Systems: Efficiency of Cell Reassociation and Endocrine Cell Topography of Rat Islet‐like Aggregates

S. Matta, G. Bauer, J. Wobken, 1994, Pancreas.

Activation of the Hypothalamic-Pituitary-Adrenal Axis by Nicotine: Neurochemical and Neuroanatomical Substrates

S. Matta, B. Sharp, 1995 .

Expression of delta opioid receptors by splenocytes from SEB-treated mice and effects on phosphorylation of MAP kinase.

S. Matta, B. Sharp, N. Shahabi, 2000, Cellular immunology.

Prenatal alcohol exposure delays the development of the cortical barrel field in neonatal rats

R. S. Waters, Cheng X. Li, A. Elberger, 2006, Experimental Brain Research.

Redistribution of tricyclic antidepressants in rats using a drug-specific monoclonal antibody: dose-response relationship.

G. Brunn, S. Pond, D. Keyler, 1991, Drug metabolism and disposition: the biological fate of chemicals.

Nicotine Self-Administration Differentially Regulates Hypothalamic Corticotropin-Releasing Factor and Arginine Vasopressin mRNAs and Facilitates Stress-Induced Neuronal Activation

Hao Chen, Wenyuan Zhao, S. Matta, 2008, The Journal of Neuroscience.

Chronic self-administration of nicotine in rats impairs T cell responsiveness.

D. Kracko, S. Singh, M. Sopori, 2002, The Journal of pharmacology and experimental therapeutics.

A central mechanism is involved in the secretion of ACTH in response to IL-6 in rats: comparison to and interaction with IL-1 beta.

J. Weatherbee, S. Matta, B. Sharp, 1992, Neuroendocrinology.

Insulin Release In Vitro from Islet Tissues and Adenomas of Rats Treated with Nicotinamide and Streptozotocin: The Effects of Glucose

S. Matta, G. Bauer, R. Younoszai, 1981, Diabetes.

Neuritogenic and metabolic effects of individual gangliosides and their interaction with nerve growth factor in cultures of neuroblastoma and pheochromocytoma.

F. Roisen, S. Matta, G. Yorke, 1986, Brain research.

Kv3-like potassium channels are required for sustained high-frequency firing in basal ganglia output neurons.

F. Zhou, S. Matta, Shengyuan Ding, 2011, Journal of neurophysiology.

A single intramuscular injection of rAAV‐mediated mutant erythropoietin protects against MPTP‐induced parkinsonism

S. Matta, T. Rex, A. Dhanushkodi, 2012, Genes, brain, and behavior.

The role of the fourth cerebroventricle in nicotine-stimulated prolactin release in the rat: involvement of catecholamines.

S. Matta, B. Sharp, 1992, The Journal of pharmacology and experimental therapeutics.

Printed in U.S.A. Copyright © 1997 by The Endocrine Society Adrenocorticotropin Response and Nicotine-Induced Norepinephrine Secretion in the Rat Paraventricular Nucleus Are Mediated through Brainstem Receptors*

S. Matta, B. Sharp, J. Valentine, 2022 .

Nicotine-induced cFos expression in the hypothalamic paraventricular nucleus is dependent on brainstem effects: correlations with cFos in catecholaminergic and noncatecholaminergic neurons in the nucleus tractus solitarius.

S. Matta, B. Sharp, J. Valentine, 1996, Endocrinology.

Guidelines on nicotine dose selection for in vivo research

A. C. Collins, E. Levin, W. Schafer, 2007, Psychopharmacology.

Monospecific antibodies against a synthetic peptide predicted from the alpha-3 nicotinic receptor cDNA inhibit binding of [3H]nicotine to rat brain nicotinic cholinergic receptor.

S. Matta, B. Sharp, C. Chao, 1989, Biochemical and biophysical research communications.

Local alpha-bungarotoxin-sensitive nicotinic receptors modulate hippocampal norepinephrine release by systemic nicotine.

S. Matta, B. Sharp, Y. Fu, 1999, The Journal of pharmacology and experimental therapeutics.

Expression of Delta Opioid Receptors and Transcripts by Splenic T Cells

Ming D. Li, S. Matta, B. Sharp, 2000, Annals of the New York Academy of Sciences.

Effects on gene expression

A. Jayaraman, J. McCoy, T. Kawarai, 1994 .

Desensitization and resensitization of norepinephrine release in the rat hippocampus with repeated nicotine administration

S. Matta, B. Sharp, J. Valentine, 1998, Neuroscience Letters.

The adrenocorticotropin response to interleukin-1 beta instilled into the rat median eminence depends on the local release of catecholamines.

S. Matta, B. Sharp, J. Singh, 1990, Endocrinology.

Nicotine stimulates the expression of cFos protein in the parvocellular paraventricular nucleus and brainstem catecholaminergic regions.

S. Matta, B. Sharp, C. Foster, 1993, Endocrinology.

Fostering itself increases nicotine self-administration in young adult male rats

Hao Chen, S. Matta, B. Sharp, 2013, Psychopharmacology.

Prostaglandins mediate the ACTH response to interleukin-1-beta instilled into the hypothalamic median eminence.

J. G. McCoy, S. Matta, B. Sharp, 1994, Neuroendocrinology.

Prostaglandins mediate the adrenocorticotropin response to tumor necrosis factor in rats.

S. Matta, B. Sharp, 1993, Endocrinology.

Genetic Factors Control Nicotine Self-Administration in Isogenic Adolescent Rat Strains

Hao Chen, E. Tolley, S. Matta, 2012, PloS one.

Gene expression in accumbens GABA neurons from inbred rats with different drug‐taking behavior

S. Gong, W. Taylor, S. Matta, 2011, Genes, brain, and behavior.

Acquisition of Nicotine Self-Administration in Adolescent Rats Given Prolonged Access to the Drug

Hao Chen, S. Matta, B. Sharp, 2007, Neuropsychopharmacology.

Tumor necrosis factor-alpha is a potent ACTH secretagogue: comparison to interleukin-1 beta.

P. Peterson, C. Chao, S. Matta, 1989, Endocrinology.

Combined exposure to nicotine and ethanol throughout full gestation results in enhanced acquisition of nicotine self-administration in young adult rat offspring

A. Elberger, S. Matta, 2007, Psychopharmacology.

Nicotine Enhances the Biosynthesis and Secretion of Transthyretin from the Choroid Plexus in Rats: Implications for β-Amyloid Formation

Ming D. Li, W. Blaner, S. Matta, 2000, The Journal of Neuroscience.

An Ultra-Short Dopamine Pathway Regulates Basal Ganglia Output

F. Zhou, Ming Xu, S. Matta, 2009, The Journal of Neuroscience.

Role of the Cyclic AMP-dependent Protein Kinase in Homologous Resensitization of the β1-Adrenergic Receptor*

M. Whitt, S. Bahouth, L. Gardner, 2004, Journal of Biological Chemistry.

Gestational nicotine exposure reduces nicotinic cholinergic receptor (nAChR) expression in dopaminergic brain regions of adolescent rats

S. L. Parker, Hao Chen, Hao Chen, 2005, The European journal of neuroscience.

Nicotine-induced norepinephrine release in the rat amygdala and hippocampus is mediated through brainstem nicotinic cholinergic receptors.

S. Matta, B. Sharp, Y. Fu, 1998, The Journal of pharmacology and experimental therapeutics.

Nicotinic activation of CRH neurons in extrahypothalamic regions of the rat brain

S. Matta, B. Sharp, J. Valentine, 1997, Endocrine.

Prenatal alcohol exposure alters the size, but not the pattern, of the whisker representation in neonatal rat barrel cortex

R. S. Waters, Cheng X. Li, A. Elberger, 2005, Experimental Brain Research.

Induction and Desensitization of the c-Fos mRNA Response to Nicotine in Rat Brain

S. Matta, B. Sharp, K. Mcallen, 1993, Molecular and Cellular Neuroscience.

Nicotine self‐administration differentially modulates glutamate and GABA transmission in hypothalamic paraventricular nucleus to enhance the hypothalamic–pituitary–adrenal response to stress

Hao Chen, S. Matta, Guoliang Yu, 2010, Journal of neurochemistry.

Regulation of the messenger ribonucleic acid for corticotropin-releasing factor in the paraventricular nucleus and other brain sites of the rat.

S. Matta, B. Sharp, H. Beyer, 1988, Endocrinology.

Norepinephrine Secretion in the Hypothalamic Paraventricular Nucleus of Rats during Unlimited Access to Self-Administered Nicotine: An In Vivo Microdialysis Study

S. Matta, B. Sharp, V. Brower, 2001, The Journal of Neuroscience.

Local α-bungarotoxin-sensitive nicotinic receptors in the nucleus accumbens modulate nicotine-stimulated dopamine secretion in vivo

S. Matta, B. Sharp, W. Gao, 2000, Neuroscience.

Systemic nicotine stimulates dopamine release in nucleus accumbens: re-evaluation of the role of N-methyl-D-aspartate receptors in the ventral tegmental area.

S. Matta, B. Sharp, W. Gao, 2000, The Journal of pharmacology and experimental therapeutics.

Selective administration of nicotine into catecholaminergic regions of rat brainstem stimulates adrenocorticotropin secretion.

S. Matta, B. Sharp, C. Foster, 1993, Endocrinology.

Role of the fourth cerebroventricle in mediating rat plasma ACTH responses to intravenous nicotine.

S. Matta, B. Sharp, K. Mcallen, 1990, The Journal of pharmacology and experimental therapeutics.

Role of the cyclic AMP-dependent protein kinase in homologous resensitization of the beta1-adrenergic receptor.

M. Whitt, S. Bahouth, L. Gardner, 2004, The Journal of biological chemistry.

Expression of three carnitine palmitoyltransferase-I isoforms in 10 regions of the rat brain during feeding, fasting, and diabetes.

S. Matta, G. Cook, Eduard N. Lavrentyev, 2004, Biochemical and biophysical research communications.

Running title : Potassium channels in basal ganglia output neurons

F. Zhou, S. Matta, Shengyuan Ding, 2010 .

Full‐gestational exposure to nicotine and ethanol augments nicotine self‐administration by altering ventral tegmental dopaminergic function due to NMDA receptors in adolescent rats

Hao Chen, S. Matta, B. Sharp, 2014, Journal of neurochemistry.

Pallidusin Projecting Neurons From the Globus + Activating Component of the Delayed Rectifier K

F. Zhou, C. Kaczorowski, H. Moreno, 2015 .

Constitutively Active TRPC3 Channels Regulate Basal Ganglia Output Neurons

F. Zhou, Fu-Ming Zhou, Fu-Wen Zhou, 2008, The Journal of Neuroscience.

The brain-immune axis: role of opiates and other substances of abuse, the hypothalamic-pituitary-adrenal axis and behavior.

D. Lysle, D. Saphier, S. Matta, 1995, Advances in experimental medicine and biology.

The Role of Gangliosides in Neurotrophic Interaction in Vitro

M. Rapport, F. Roisen, S. Matta, 1986 .

Kv3-like potassium channels are required for sustained high-frequency firing in basal ganglia output neurons.

F. Zhou, S. Matta, Shengyuan Ding, 2011, Journal of neurophysiology.

An Ultra-Short Dopamine Pathway Regulates Basal Ganglia Output

F. Zhou, Ming Xu, S. Matta, 2009, The Journal of Neuroscience.

Catecholamines mediate nicotine-induced adrenocorticotropin secretion via alpha-adrenergic receptors.

S. Matta, B. Sharp, Jasbir Singh, 1990, Endocrinology.

Nicotine elevates rat plasma ACTH by a central mechanism.

S. Matta, B. Sharp, K. Mcallen, 1987, The Journal of pharmacology and experimental therapeutics.

Adrenocorticotropin response and nicotine-induced norepinephrine secretion in the rat paraventricular nucleus are mediated through brainstem receptors.

S. Matta, B. Sharp, J. Valentine, 1997 .