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Mu-opioid receptor knockout mice show diminished food-anticipatory activity.

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Title: Mu-opioid receptor knockout mice show diminished food-anticipatory activity.
Authors: Kas, Martien J. H. (AUTHOR), Van Den Bos, Ruud (AUTHOR), Baars, Annemarie M. (AUTHOR), Lubbers, Marianne (AUTHOR), Lesscher, Heidi M. B. (AUTHOR), Hillebrand, Jacquelien J. G. (AUTHOR), Schuller, Alwin G. (AUTHOR), Pintar, John E. (AUTHOR), Spruijt, Berry M. (AUTHOR)
Source: European Journal of Neuroscience. Sep2004, Vol. 20 Issue 6, p1624-1632. 9p.
Subjects: Neurobiology, Neurosciences, Molecular neurobiology, Neurophysiology, Dopaminergic neurons, Neurotransmitter receptors
Abstract: We have previously suggested that during or prior to activation of anticipatory behaviour to a coming reward,µ-opioid receptors are activated. To test this hypothesis schedule induced food-anticipatory activity inµ-opioid receptor knockout mice was measured using running wheels. We hypothesized thatµ-knockout mice show little food-anticipatory activity. In wildtype mice we observed that food-anticipatory activity increased proportional to reduced food intake levels during daily scheduled food access, and thus reflects the animal's physiological need for food.µ-Knockout mice do not adjust their schedule induced running wheel behaviour prior to and during feeding time in the same way as wildtype mice; rather than showing more running wheel activity before than during feeding, they showed an equal amount of activity before and during feeding. As food-anticipatory activity is dependent on the mesolimbic dopamine system andµ-opioid receptors regulate dopaminergic activity, these data suggest a change in the dopamine system's activity inµ-knockout mice. As we observed thatµ-knockout mice tended to show a stronger locomotor activity response than wildtype mice to the indirect dopamine agonistd-amphetamine, it appears that the dopaminergic systemper seis intact and sensitive to activation. We found no differences in the expression of pro-opiomelanocortin, a precursor of endogenous endorphin, in the arcuate nucleus betweenµ-knockout mice and wildtype mice during restricted feeding, showing that theµ-opioid receptor does not regulate endogenous endorphin levels. These data overall suggest a role forµ-opioid receptors in adapting reward related behaviour to the requirements of the environment. [ABSTRACT FROM AUTHOR]
Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Mu-opioid receptor knockout mice show diminished food-anticipatory activity.
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  Data: <searchLink fieldCode="AR" term="%22Kas%2C+Martien+J%2E+H%2E%22">Kas, Martien J. H.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Van+Den+Bos%2C+Ruud%22">Van Den Bos, Ruud</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Baars%2C+Annemarie+M%2E%22">Baars, Annemarie M.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lubbers%2C+Marianne%22">Lubbers, Marianne</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lesscher%2C+Heidi+M%2E+B%2E%22">Lesscher, Heidi M. B.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hillebrand%2C+Jacquelien+J%2E+G%2E%22">Hillebrand, Jacquelien J. G.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schuller%2C+Alwin+G%2E%22">Schuller, Alwin G.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pintar%2C+John+E%2E%22">Pintar, John E.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Spruijt%2C+Berry+M%2E%22">Spruijt, Berry M.</searchLink> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Neuroscience%22">European Journal of Neuroscience</searchLink>. Sep2004, Vol. 20 Issue 6, p1624-1632. 9p.
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  Data: We have previously suggested that during or prior to activation of anticipatory behaviour to a coming reward,µ-opioid receptors are activated. To test this hypothesis schedule induced food-anticipatory activity inµ-opioid receptor knockout mice was measured using running wheels. We hypothesized thatµ-knockout mice show little food-anticipatory activity. In wildtype mice we observed that food-anticipatory activity increased proportional to reduced food intake levels during daily scheduled food access, and thus reflects the animal's physiological need for food.µ-Knockout mice do not adjust their schedule induced running wheel behaviour prior to and during feeding time in the same way as wildtype mice; rather than showing more running wheel activity before than during feeding, they showed an equal amount of activity before and during feeding. As food-anticipatory activity is dependent on the mesolimbic dopamine system andµ-opioid receptors regulate dopaminergic activity, these data suggest a change in the dopamine system's activity inµ-knockout mice. As we observed thatµ-knockout mice tended to show a stronger locomotor activity response than wildtype mice to the indirect dopamine agonistd-amphetamine, it appears that the dopaminergic systemper seis intact and sensitive to activation. We found no differences in the expression of pro-opiomelanocortin, a precursor of endogenous endorphin, in the arcuate nucleus betweenµ-knockout mice and wildtype mice during restricted feeding, showing that theµ-opioid receptor does not regulate endogenous endorphin levels. These data overall suggest a role forµ-opioid receptors in adapting reward related behaviour to the requirements of the environment. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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