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 inBrain research. Molecular brain research. Vol. 86; no. 1-2; pp. 70 - 75
Main Authors Sharifi, Nima, Diehl, Nicole, Yaswen, Linda, Brennan, Miles B., Hochgeschwender, Ute
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 31.01.2001
Elsevier
Subjects
Online AccessGet full text
ISSN0169-328X
1872-6941
DOI10.1016/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.
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
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  fullname: Yaswen, Linda
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  surname: Hochgeschwender
  fullname: Hochgeschwender, Ute
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  organization: Developmental Biology Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK 73104, USA
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Issue 1-2
Keywords Mouse
RT/PCR
Homologous targeting
Vertebrata
Mammalia
Targeting
Gene
Rodentia
Dynorphin
Peptidergic receptor
Mutation
Neuropeptide
Opioid peptide
Language English
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Snippet The opioid system has important roles in controlling pain, reward and addiction, and is implicated in numerous other processes within and outside the nervous...
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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
Title Generation of dynorphin knockout mice
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0169328X00002643
https://dx.doi.org/10.1016/S0169-328X(00)00264-3
https://www.ncbi.nlm.nih.gov/pubmed/11165373
https://www.proquest.com/docview/17776172
https://www.proquest.com/docview/70645570
Volume 86
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