PSYCHIATRY

 

 

Publication Record

 

Al-Amin, H. A., C. Shanon-Weiket*, D. R. Weinberger*, and B. K. Lipska*. 2001. Delayed onset of enhanced MK-801 induced motor hyperactivity after neonatal lesions of the rat ventral hippocampus. Biological Psychiatry 49 (6):528–539.

Al-Amin, H. A., and D. R. Weinberger*. 2000. Chapter 1: Advances in schizophrenia research. Psychopharmacology of Schizophrenia, Eds. M. Reveley and B. Deakin. Arnold Publishers.

Al-Amin, H. A., D. R. Weinberger*, and B. K. Lipska*. 2000. Exaggerated MK-801-induced motor hyperactivity in rats with the neonatal lesion of the ventral hippocampus. Behavioral Pharmacology 11 (3–4):269–278.

 

 

 

Abstracts, Conferences, and Proceedings

 

Al-Amin, H. A., M. Khani, and N. Damluji. July 1999. Mental health post-war in Lebanon: Focus on panic disorder and depression. The National Arab American Medical Association, 16th International Medical Convention, Beirut, Lebanon.

Al-Amin, H. A., N. E. Saadé, M. Jaber*, B. Bouhadir, S. J. Jabbur, and S. F. Atweh. December 2000. Acute and chronic effects of the NMDA antagonist dizocilpine on the sensorimotor behaviors in rats. The Lebanese Association for the Advancement of Science, 14th Science Meeting, Beirut, Lebanon.

Al-Amin, H. A., N. E. Saadé, C. A. Massaad, M. K. Khani, S. J. Jabbur, and S. F. Atweh. November 2000. Dopamine D1 and D2 receptors modulate the response to acute pain in rats. Society of Neuroscience, New Orleans, Louisiana, USA.

 

 

Research Projects

 

Neurodevelopmental perspectives of the neonatal ventral hippocampus lesion as an animal model of schizophrenia

Abnormal neurodevelopment has been suggested to play a major role in the pathophysiology of schizophrenia.  The glutamate NMDA system, which has also been implicated in schizophrenia, is an integral part of neurodevelopment and cortical maturation.  Various abnormal behaviors in schizophrenia can be modeled in animals treated with NMDA antagonists and/or dopamine agonists.  The neonatal lesion of ventral hippocampus (VH)—an animal model of schizophrenics—can be used to study the impact of early cortical lesion on the neurodevelopment of various brain systems. The aims of this project are 1) to study the pain threshold in the neonatal and adult VH lesioned rats, 2) to study the effects of the noncompetitive NMDA antagonist dizocilpine (MK-801) on pain threshold, locomotion, and stereotypy in adult rats with neonatal VH lesion, and 3) to study the developmental changes in the NMDA, dopamine, and opiate receptors in different brain regions after neonatal and adult VH lesions. Al-Amin, H. A., S. Atweh, and M. Khani.

Supported by URB, LNCSR, AUB Medical Practice Plan, Diana Tamari Sabbagh and Massabki Funds
Completed or in progress at AUB

 

Risperidone in chronic schizophrenic subjects previously on treatment with conventional oral antipsychotic medications

This is a multicenter international study on the efficacy and tolerance of Risperidone, a serotonin-dopamine antagonist, in comparison to the classical dopamine antagonists in the treatment of chronic schizophrenia. Al-Amin, H. A., and M. Khani.


Supported by Janssen Pharmaceutica
Completed or in progress at AUB

 

Behavioral, cellular, and molecular effects of addictive substances on sensorimotor processes: Modulation by environmental and pharmacological factors

The mesocorticolimbic circuitry has been implicated in the pathophysiology of several neuropsychiatric syndromes, such as drug addiction and central pain.  Behavioral studies have shown that alteration in the dopamine/glutamate interactions at both the cortical and subcortical levels can modulate the mesocorticolimbic circuitry.  We propose the following approaches to investigate the dopaminergic and glutamatergic mechanisms involved in sensorimotor integration and their relations to addiction and pain:  a) effects of acute and chronic administration of psychostimulants on motor behavior and pain tests, b) modulation of the above-mentioned behavior by different environmental, anatomical, and pharmacological interventions, and c) correlation of the above-mentioned behavioral effects with changes in the cellular and molecular mechanisms involved in the activity of the dopamine, glutamate, and opiate systems.  Such mechanisms include gene expression and immunoreactivity of the various receptors of the latter systems, at both the cortical and subcortical levels.  Al-Amin, H. A., M. Khani, S. Atweh, and S. Jabbur.

Supported by Cooperation pour L’Evaluation et la Développement de la Recherche
Completed or in progress at AUB