脊髄後角アストロサイトのαおよびβアドレナリン受容体を介する異なる痛覚制御
Pain transmission in the spinal dorsal horn (SDH) is powerfully controlled by descending neurons from the brain. One major neurotransmitter of the descending pathways is noradrenaline (NA). Traditionally, NA is known to produce an analgesic effect, but we recently demonstrated that NA also induces a...
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Published in | 日本薬理学会年会要旨集 p. 3-O-105 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
公益社団法人 日本薬理学会
2022
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Abstract | Pain transmission in the spinal dorsal horn (SDH) is powerfully controlled by descending neurons from the brain. One major neurotransmitter of the descending pathways is noradrenaline (NA). Traditionally, NA is known to produce an analgesic effect, but we recently demonstrated that NA also induces a pronociceptive effect via α1A-adrenoceptors (α1A-ARs) in SDH astrocytes expressing Hes5. Therefore, the mechanism for bidirectional modulation by NA is entirely unknown. In this study, we found that intrathecal injection of NA at a low dose induced mechanical hypersensitivity, which required α1A-ARs in Hes5+ astrocytes. On the other hand, at a high dose of intrathecal NA, the hypersensitivity disappeared. Interestingly, this effect of the high dose of NA was not affected by lacking α1A-ARs in Hes5+ astrocytes, but was prevented by pharmacological inhibition of spinal β1-ARs or genetic knockout of astrocytic β1-ARs. Furthermore, mechanical hypersensitivity by chronic stress was suppressed and exacerbated by astrocytic α1A- and β1-AR-knockout, respectively. Our findings suggest that the bidirectional pain control by spinal NA is dependent on the levels of NA and the different types of astrocytic adrenoceptors. |
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AbstractList | Pain transmission in the spinal dorsal horn (SDH) is powerfully controlled by descending neurons from the brain. One major neurotransmitter of the descending pathways is noradrenaline (NA). Traditionally, NA is known to produce an analgesic effect, but we recently demonstrated that NA also induces a pronociceptive effect via α1A-adrenoceptors (α1A-ARs) in SDH astrocytes expressing Hes5. Therefore, the mechanism for bidirectional modulation by NA is entirely unknown. In this study, we found that intrathecal injection of NA at a low dose induced mechanical hypersensitivity, which required α1A-ARs in Hes5+ astrocytes. On the other hand, at a high dose of intrathecal NA, the hypersensitivity disappeared. Interestingly, this effect of the high dose of NA was not affected by lacking α1A-ARs in Hes5+ astrocytes, but was prevented by pharmacological inhibition of spinal β1-ARs or genetic knockout of astrocytic β1-ARs. Furthermore, mechanical hypersensitivity by chronic stress was suppressed and exacerbated by astrocytic α1A- and β1-AR-knockout, respectively. Our findings suggest that the bidirectional pain control by spinal NA is dependent on the levels of NA and the different types of astrocytic adrenoceptors. |
Author | 津田, 誠 川邉, 陸 吉原, 康平 古賀, 啓祐 白坂, 亮二 内山, 瑳和子 |
Author_xml | – sequence: 1 fullname: 吉原, 康平 organization: 九州大・院薬・薬理 – sequence: 2 fullname: 川邉, 陸 organization: 九州大・院薬・薬理 – sequence: 3 fullname: 内山, 瑳和子 organization: 九州大・院薬・薬理 – sequence: 4 fullname: 白坂, 亮二 organization: 九州大・院薬・薬理 – sequence: 5 fullname: 古賀, 啓祐 organization: 兵庫医科大・神経生理 – sequence: 6 fullname: 津田, 誠 organization: 九州大・院薬・薬理 |
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SubjectTerms | astrocyte noradrenaline (norepinephrine) pain stress |
Title | 脊髄後角アストロサイトのαおよびβアドレナリン受容体を介する異なる痛覚制御 |
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