JP2022502365A - カルバメート化合物及びそれを含む製剤の急性ストレス障害又は心的外傷後ストレス障害の予防、軽減又は治療のための使用 - Google Patents
カルバメート化合物及びそれを含む製剤の急性ストレス障害又は心的外傷後ストレス障害の予防、軽減又は治療のための使用 Download PDFInfo
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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Abstract
Description
(式中、R1及びR2は、それぞれ独立して、水素、ハロゲン、C1−C8アルキル、C1−C8ハロアルキル、C1−C8チオアルコキシ及びC1−C8アルコキシからなる群から選ばれ、A1及びA2の一つは、CHであり、他の一つはNである)
で示されるカルバメート化合物、又はその薬学的に許容可能な塩、溶媒和物又は水和物を含む、急性ストレス障害又は心的外傷後ストレス障害の予防、軽減又は治療用薬剤を提供する。
(式中、R1及びR2は、それぞれ独立して、水素、ハロゲン、C1−C8アルキル、C1−C8ハロアルキル、C1−C8チオアルコキシ及びC1−C8アルコキシからなる群から選ばれ、A1及びA2の一つは、CHであり、他の一つはNである)
で示されるカルバメート化合物、又はその薬学的に許容可能な塩、溶媒和物又は水和物;及び
(b)選択的セロトニン再取り込み阻害剤(SSRI);
を含む、急性ストレス障害又は心的外傷後ストレス障害の予防、軽減又は治療用組み合わせ剤が提供される。
(式中、R1及びR2は、それぞれ独立して、水素、ハロゲン、C1−C8アルキル、C1−C8ハロアルキル、C1−C8チオアルコキシ及びC1−C8アルコキシからなる群から選ばれ、A1及びA2の一つは、CHであり、他の一つはNである)
で示されるカルバメート化合物、又はその薬学的に許容可能な塩、溶媒和物又は水和物を含む、心的外傷後ストレス障害の症状の予防、軽減又は治療用薬剤が提供される。
以下で、本願発明について、実施例を通じてより詳細に説明する。しかし、以下の実施例は、一つ以上の実施形態を例示的に説明することのみを意図しており、本発明の範囲を限定することを意図していない。
カルバミン酸(R)−1−(2−クロロフェニル)−2−テトラゾール−2−イル)エチルエステル(以下、「試験化合物」という)を国際公開番号WO2010/150946号の製造例50に記載された方法に従って製造した。
実験動物
成体雄性ラット(Sprague-Dawley、200−230g)を使用した。実験動物は、12時間の明暗周期(午後7時から午前7時まで照明)、22〜25℃の温度、40〜60%の相対湿度に維持され、水と餌は自由にアクセスできるようにした。動物は、以下のようにランダムに3つの群に分けられた:
−対照群として、投与ビヒクル(vehicle)としての食塩水(saline)を3mL/kg用量で経口投与した14匹のラット(第1群)
−心的外傷後ストレス障害誘発後に、投与ビヒクル(vehicle)としての食塩水(saline)を3mL/kg用量で経口投与した12匹のラット(第2群)
−心的外傷後ストレス障害誘発後に、試験化合物を30mg/kg(3mL/kg)用量で経口投与した12匹のラット(第3群)。
最適な心的外傷後ストレス障害を確立するために、単一長期ストレス(SPS)によって誘発した。様々な条件の(拘束ストレス2時間、強制水泳20分、休息15分、エーテル露出)ストレスに暴露させて、心的外傷後ストレス障害が発現した動物モデルを樹立した。
単一長期ストレスへの暴露の翌日から15日間、第2群にビヒクルとして食塩水を、第3群に製造礼の化合物30mg/kg(3mL/kg)を経口投与した。
一方、心的外傷後ストレス障害が誘発されなかった第1群は、第2群及び第3群で経口投与開始日と同時に、食塩水を経口投与した。
前記第1群〜第3群のラットに対する強制水泳試験のために、25℃の水を透明なシリンダー(直径20cm×高さ50cm)に高さ30cmまで満たした。強制水泳試験は、2つのセッションで構成される。初日、ラットを水で満たされたシリンダー内で15分間順応させた。24時間後、ラットを5分間シリンダーに入れ、ラットの逃避行動脱出しようとする行動(escape behavior)を、ビデオカメラを使用して記録し、測定した。ラットの行動は、よじ登り、不動、水泳の行動に区分して分析した。よじ登り行動は上に上る時間を測定し、不動の行動は逃避行動を示さない時間を測定し、水泳の行動はシリンダー内で水平に移動する時間を測定した。その結果をそれぞれ図1〜図3に示した。
化合物の有効性は、平均±標準誤差(SEM)として表され、データにP<0.05の差がある場合に統計学的有効性が認識された。統計学的解析は、プリズム7.04の一元配置分散分析を使用して行った。
実験動物
成体雄性ラット(Sprague-Dawley、200−230g)を使用した。実験動物は、12時間の明暗周期(午後7時から午前7時まで照明)、22〜25℃の温度、40〜60%の相対湿度に維持され、水と餌は自由にアクセスできるようにした。動物は、以下のようにランダムに3つの群に分けられた:
−対照群として、投与ビヒクルとしての食塩水を3mL/kg用量で経口投与した8匹のラット
−心的外傷後ストレス障害誘発後に、投与ビヒクルとしての食塩水を3mL/kg用量で経口投与した7匹のラット
−心的外傷後ストレス障害誘発後に、試験化合物を30mg/kg(3mL/kg)用量で経口投与した7匹のラット。
最適な心的外傷後ストレス障害を確立するために、単一長期ストレス(SPS)によって誘発した。様々な条件の(拘束ストレス2時間、強制水泳20分、休息15分、エーテル露出)ストレスに暴露させて、心的外傷後ストレス障害が発現した動物モデルを樹立した。
単一長期ストレスへの暴露の翌日から15日間、第2群にビヒクルとして食塩水を、第3群に製造礼の化合物30mg/kg(3mL/kg)を経口投与した。
強制水泳試験の翌日に断頭によりラットを急速に犠牲にし、腹部大動脈から血液を迅速に採取した。血液サンプルを4000gで10分間遠心分離し、血清を採取して−20℃で保存した。コルチコイド濃度は、Novus Biologicals Corticosterone kitを使用した酵素結合免疫分析法(ELISA)によって測定された。コルチコイド濃度を計算するために、ELISAリーダー(MultiRead 400)を使用して測定した。
化合物の有効性は、平均±標準誤差(SEM)として表され、データにP<0.05の差がある場合に統計学的有効性が認識された。統計学的解析は、プリズム7.04の一元配置分散分析を使用して行った。
実験動物
成体マウス(CD−1)を使用した。実験動物は、12時間の明暗周期(午後7時から午前7時まで照明)、22〜25℃の温度、40〜60%の相対湿度に維持され、水と餌は自由にアクセスできるようにした。動物は、以下のようにランダムに4つの群に分けられた:
−対照群として、投与ビヒクルとしての食塩水を10mL/kg用量で腹腔内注射投与した8匹のマウス
−実験群として、試験化合物を5mg/kg(10mL/kg)用量で腹腔内注射投与した8匹のマウス
−実験群として、フルオキセチン塩酸塩を10mg/kg(10mL/kg)用量で腹腔内注射投与した8匹のマウス
−実験群として、試験化合物を5mg/kg(10mL/kg)用量とフルオキセチン塩酸塩を10mg/kg(10mL/kg)用量を一緒に腹腔内注射で投与した8匹のマウス。
前記第1群〜第4群のマウスで強制水泳試験を行うために、25℃の水を透明なシリンダーに高さ20cmまで満たした。投薬30分後、マウスを水中で2分間順応させ、動かなかった絶望行動(despair behavior)の持続時間をタイマーを利用して4分間測定した。その結果を図5に示した。
化合物の有効性は、平均±標準誤差(SEM)として表され、データにP<0.05の差がある場合に統計学的な有効性が認識された。統計学的解析は、プリズム7.04の一元配置分散分析を使用して行った。
Claims (13)
- R1及びR2が、それぞれ独立して、水素、ハロゲン及びC1−C8アルキルからなる群から選ばれる、請求項1に記載の薬剤。
- 選択的セロトニン再取り込み阻害剤が、フルオキセチン(fluoxetine)、セルトラリン(sertraline)、パロキセチン(paroxetine)及びそれらの薬学的に許容される塩からなる群から1種以上選ばれることを特徴とする、請求項4に記載の組み合わせ剤。
- (a):(b)の重量比が、1000:1〜1:1000の範囲内であることを特徴とする、請求項4に記載の組み合わせ剤。
- (a):(b)の重量比が、100:1〜1:100の範囲内であることを特徴とする、請求項6に記載の組み合わせ剤。
- 式(1)の化合物を遊離形態に基づいて、12.5mg〜500mgの量で含むことを特徴とする、請求項4に記載の組み合わせ剤。
- 選択的セロトニン再取り込み阻害剤が、フルオキセチン又はその薬学的に許容される塩であることを特徴とする、請求項5に記載の組み合わせ剤。
- 選択的セロトニン再取り込み阻害剤が、フルオキセチン塩酸塩であることを特徴とする、請求項9に記載の組み合わせ剤。
- フルオキセチンを遊離形態に基づいて、10mg〜60mgの量で含むことを特徴とする、請求項9に記載の組み合わせ剤。
- 心的外傷後ストレス障害の症状が、外傷的出来事の全部又は部分的記憶喪失(amnesia)、外傷的出来事を再経験する患者におけるフラッシュバック(flashback)又は外傷的出来事に関連する刺激の回避(avoidance)、悪夢(nightmare)、過敏性(irritability)、過覚醒(hyperarousal)、過度の用心深さ(hypervigilance)、怒り、集中力低下及び感情的引きこもり(emotional withdrawal)からなる群から選ばれる1種以上であることを特徴とする、請求項12に記載の薬剤。
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