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Decreased motivational value in an instrumental task after a single injection of haloperidol with quantitative assessment of dopamine D2-like receptor occupancy

https://repo.qst.go.jp/records/70942
https://repo.qst.go.jp/records/70942
3b3f25b6-3d3d-4f57-90da-07e4352d6835
Item type 会議発表用資料 / Presentation(1)
公開日 2012-10-23
タイトル
タイトル Decreased motivational value in an instrumental task after a single injection of haloperidol with quantitative assessment of dopamine D2-like receptor occupancy
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Hori, Yukiko

× Hori, Yukiko

WEKO 697113

Hori, Yukiko

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Nagai, Yuji

× Nagai, Yuji

WEKO 697114

Nagai, Yuji

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Oh-Nishi, Arata

× Oh-Nishi, Arata

WEKO 697115

Oh-Nishi, Arata

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Suhara, Tetsuya

× Suhara, Tetsuya

WEKO 697116

Suhara, Tetsuya

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Minamimoto, Takafumi

× Minamimoto, Takafumi

WEKO 697117

Minamimoto, Takafumi

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堀 由紀子

× 堀 由紀子

WEKO 697118

en 堀 由紀子

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永井 裕司

× 永井 裕司

WEKO 697119

en 永井 裕司

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大西 新

× 大西 新

WEKO 697120

en 大西 新

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須原 哲也

× 須原 哲也

WEKO 697121

en 須原 哲也

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南本 敬史

× 南本 敬史

WEKO 697122

en 南本 敬史

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抄録
内容記述タイプ Abstract
内容記述 The motivation to engage in action is regulated by valuation of predicted outcome comprised from external factor (i.e., incentive) and internal factor (i.e., drive). Function-mediated dopamine D2-like receptor (D2R) is widely known to be involved in processing motivation, incentive, and drive. However, it is unclear how the transmission via D2R is related to the computation of motivational value from these factors. To address this issue, we quantitatively assessed the relationship between motivational value of instrumental action and dopamine D2-like receptor availability after systemic injection of D2R antagonist. We performed positron emission tomography (PET) measurements for D2R binding with [11C]raclopride in 2 monkeys. With a systemic injection of a low dose of D2R antagonist, haloperidol (0.01mg/kg, i.m.), occupancy of D2R in the striatum was 74~81%. This occupancy lasted to at least post-injection day 3 (~40% occupancy), and [11C]raclopride binding recovered to the pre-treatment level at day 7. We tested 2 monkeys with reward-size task (Minamimoto et al., 2009), in which they were required to release a bar to receive predicted water rewards (1, 2, 4 or 8 drops). The error rate of the task (i.e., proportion of trials with low motivation) increased during days 0 to 3 after the haloperidol injection. We quantified the motivational value by using error rate (E), since it is inversely related to the predicted reward size (R): E = 1/aR, where a is a free parameter. The best-fit parameter a was discounted from the pre-treatment level by 50% at day 0 and by 30~40% at day 3, returning to the pre-treatment level at day 7, suggesting that the impact of outcome on motivational value attenuated in parallel with D2R occupancy. In contrast, the injection of haloperidol did not affect sucrose preference or water amount intake in the home cage, indicating that incentive valence and drive were unimpaired. These results suggest that attenuation of dopamine transmission via D2 receptors reduces computation of motivational value from external and internal information.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Neuroscience 2012, SfN's 42th annual meeting
発表年月日
日付 2012-10-17
日付タイプ Issued
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