Generation of dynorphin knockout mice
The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least...
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Published in | Brain research. Molecular brain research. Vol. 86; no. 1-2; pp. 70 - 75 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
31.01.2001
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0169-328X 1872-6941 |
DOI | 10.1016/S0169-328X(00)00264-3 |
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Abstract | The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least three ligands, enkephalin, endorphin, and dynorphin, which act through the opioid receptors μ, δ, and κ. In order to dissect the roles of individual components of the opioid system, mutant mice lacking single ligands or receptors are instrumental. We report here on the generation and initial characterization of a mutant mouse strain lacking pre-prodynorphin. Dynorphin ‘knockout’ mice are viable, healthy, and fertile and show no overt behavioral differences to wildtype littermates. Dynorphin knockout mice constitute a valuable tool for many research areas, among them research into pain, substance abuse, and epilepsy. |
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AbstractList | The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least three ligands, enkephalin, endorphin, and dynorphin, which act through the opioid receptors mu, delta, and kappa. In order to dissect the roles of individual components of the opioid system, mutant mice lacking single ligands or receptors are instrumental. We report here on the generation and initial characterization of a mutant mouse strain lacking pre-prodynorphin. Dynorphin 'knockout' mice are viable, healthy, and fertile and show no overt behavioral differences to wildtype littermates. Dynorphin knockout mice constitute a valuable tool for many research areas, among them research into pain, substance abuse, and epilepsy. The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least three ligands, enkephalin, endorphin, and dynorphin, which act through the opioid receptors μ, δ, and κ. In order to dissect the roles of individual components of the opioid system, mutant mice lacking single ligands or receptors are instrumental. We report here on the generation and initial characterization of a mutant mouse strain lacking pre-prodynorphin. Dynorphin ‘knockout’ mice are viable, healthy, and fertile and show no overt behavioral differences to wildtype littermates. Dynorphin knockout mice constitute a valuable tool for many research areas, among them research into pain, substance abuse, and epilepsy. The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least three ligands, enkephalin, endorphin, and dynorphin, which act through the opioid receptors mu, delta, and kappa. In order to dissect the roles of individual components of the opioid system, mutant mice lacking single ligands or receptors are instrumental. We report here on the generation and initial characterization of a mutant mouse strain lacking pre-prodynorphin. Dynorphin 'knockout' mice are viable, healthy, and fertile and show no overt behavioral differences to wildtype littermates. Dynorphin knockout mice constitute a valuable tool for many research areas, among them research into pain, substance abuse, and epilepsy.The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous system, such as mood states, immune responses, and prenatal developmental processes. The effects of the opioid system are mediated by at least three ligands, enkephalin, endorphin, and dynorphin, which act through the opioid receptors mu, delta, and kappa. In order to dissect the roles of individual components of the opioid system, mutant mice lacking single ligands or receptors are instrumental. We report here on the generation and initial characterization of a mutant mouse strain lacking pre-prodynorphin. Dynorphin 'knockout' mice are viable, healthy, and fertile and show no overt behavioral differences to wildtype littermates. Dynorphin knockout mice constitute a valuable tool for many research areas, among them research into pain, substance abuse, and epilepsy. |
Author | Brennan, Miles B. Hochgeschwender, Ute Diehl, Nicole Sharifi, Nima Yaswen, Linda |
Author_xml | – sequence: 1 givenname: Nima surname: Sharifi fullname: Sharifi, Nima organization: Unit on Molecular Genetics, Clinical Neuroscience Branch, NIMH, 49 Convent Drive, Bethesda, MD 20892, USA – sequence: 2 givenname: Nicole surname: Diehl fullname: Diehl, Nicole organization: Unit on Molecular Genetics, Clinical Neuroscience Branch, NIMH, 49 Convent Drive, Bethesda, MD 20892, USA – sequence: 3 givenname: Linda surname: Yaswen fullname: Yaswen, Linda organization: Unit on Molecular Genetics, Clinical Neuroscience Branch, NIMH, 49 Convent Drive, Bethesda, MD 20892, USA – sequence: 4 givenname: Miles B. surname: Brennan fullname: Brennan, Miles B. organization: Eleanor Roosevelt Institute, 1899 Gaylord Street, Denver, CO 80206, USA – sequence: 5 givenname: Ute surname: Hochgeschwender fullname: Hochgeschwender, Ute email: uteh@omrf.ouhsc.edu organization: Developmental Biology Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK 73104, USA |
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Keywords | Mouse RT/PCR Homologous targeting Vertebrata Mammalia Targeting Gene Rodentia Dynorphin Peptidergic receptor Mutation Neuropeptide Opioid peptide |
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SubjectTerms | Animals Biological and medical sciences Brain Chemistry - genetics Cell receptors Cell structures and functions Dynorphins - genetics Fundamental and applied biological sciences. Psychology Gene Expression - physiology Homologous targeting Mice Mice, Inbred C57BL Mice, Knockout - genetics Molecular and cellular biology Mouse Neuropeptide receptors Protein Precursors - genetics Reverse Transcriptase Polymerase Chain Reaction RT/PCR Stem Cells - physiology |
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