JPWO2020045612A1 - 間欠的持久力向上剤または血中pH上昇剤 - Google Patents
間欠的持久力向上剤または血中pH上昇剤 Download PDFInfo
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- JPWO2020045612A1 JPWO2020045612A1 JP2020539613A JP2020539613A JPWO2020045612A1 JP WO2020045612 A1 JPWO2020045612 A1 JP WO2020045612A1 JP 2020539613 A JP2020539613 A JP 2020539613A JP 2020539613 A JP2020539613 A JP 2020539613A JP WO2020045612 A1 JPWO2020045612 A1 JP WO2020045612A1
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- Prior art keywords
- aspartic acid
- weight
- blood
- tyrosine
- present
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Abstract
Description
これらに加えて、本発明者らは、アスパラギン酸が間欠的持久力を向上させる際に、対象における血中のpHが効率よく上昇していることを見出した。かかる知見に基づいてさらに研究を進めることによって本発明を完成するに至った。すなわち、本発明は以下の通りである。
[2]アスパラギン酸およびチロシンを含む、[1]記載の剤。
[3]アスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、[2]記載の剤。
[4]アスパラギン酸を含む、血中pH上昇剤。
[5]アシドーシス改善に用いられることを特徴とする、[4]記載の剤。
[6]以下からなる群から選択される1以上の疾患の治療、改善、または予防に用いられることを特徴とする、[4]または[5]記載の剤:
(1)高尿酸血症
(2)痛風。
[7][1]〜[6]のいずれかに記載の剤を含む、飲食品。
[A−1]間欠的持久力の向上用薬剤を製造するためのアスパラギン酸およびチロシンのいずれかまたは両方を含む組成物の使用。
[A−2]組成物がアスパラギン酸およびチロシンを含む、[A−1]記載の使用。
[A−3]組成物におけるアスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、[A−2]記載の使用。
[A−4]血中pH上昇用薬剤の製造のための、アスパラギン酸を含む組成物の使用。
[A−5]血中pH上昇用薬剤がアシドーシス改善用薬剤である、[A−4]記載の使用。
[A−6]血中pH上昇薬剤が、以下からなる群から選択される1以上の疾患の治療、改善、または予防用薬剤である、[A−4]または[A−5]記載の使用:
(1)高尿酸血症
(2)痛風。
[A−7]組成物が飲食品である、[A−1]〜[A−6]のいずれか記載の使用。
[B−1]間欠的持久力の向上における使用のための、アスパラギン酸およびチロシンのいずれかまたは両方を含む組成物。
[B−2]アスパラギン酸およびチロシンを含む、[B−1]記載の組成物。
[B−3]アスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、[B−2]記載の組成物。
[B−4]血中pHの上昇における使用のための、アスパラギン酸を含む、組成物。
[B−5]アシドーシス改善のための、[B−4]記載の組成物。
[B−6]以下からなる群から選択される1以上の疾患の治療、改善、または予防に用いられる、[B−4]または[B−5]記載の組成物:
(1)高尿酸血症
(2)痛風。
[B−7]組成物が飲食品である、[B−1]〜[B−6]のいずれか記載の組成物。
[C−1]対象に有効量のアスパラギン酸およびチロシンのいずれかまたは両方を投与することを含む、対象における間欠的持久力を向上させる方法。
[C−2]対象に有効量のアスパラギン酸およびチロシンを投与することを含む、[C−1]記載の方法。
[C−3]アスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、[C−2]記載の方法。
[C−4]対象に有効量のアスパラギン酸を投与することを含む、対象における血中pHを上昇させる方法。
[C−5]対象におけるアシドーシス改善のための、[C−4]記載の方法。
[C−6]以下からなる群から選択される1以上の疾患の治療、改善、または予防のための、[C−4]または[C−5]記載の方法:
(1)高尿酸血症
(2)痛風。
[C−7]アスパラギン酸およびチロシンのいずれかまたは両方が飲食品に含有されることを特徴とする、[C−1]〜[C−6]のいずれか記載の方法。
[D−1]間欠的持久力の向上のためのアスパラギン酸およびチロシンのいずれかまたは両方を含む組成物の使用。
[D−2]組成物がアスパラギン酸およびチロシンを含む、[D−1]記載の使用。
[D−3]組成物におけるアスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、[D−2]記載の使用。
[D−4]血中pHを上昇させるための、アスパラギン酸を含む組成物の使用。
[D−5]血中pHの上昇がアシドーシスを改善させるためである、[D−4]記載の使用。
[D−6]組成物が飲食品である、[D−1]〜[D−5]のいずれか記載の使用。
本発明は、アスパラギン酸およびチロシンのいずれかまたは両方を含む、間欠的持久力向上剤(以下、「本発明の間欠的持久力向上剤」と称することがある)を提供する。
本発明はまた、アスパラギン酸を含む、血中pH上昇剤(以下、「本発明の血中pH上昇剤」と称することがある)を提供する。
崩壊剤としては、たとえば、クロスポビドン、ポビドン、結晶セルロース等が挙げられる。滑沢剤としては、たとえば、タルク、ステアリン酸マグネシウム等が挙げられる。被覆剤としては、たとえば、メタクリル酸・メタクリル酸メチル共重合体、メタクリル酸・アクリル酸エチル共重合体、メタクリル酸メチル・メタクリル酸ブチル・メタクリル酸ジメチルアミノエチル共重合体、アクリル酸エチル・メタクリル酸メチル・メタクリル酸塩化トリメチルアンモニウムエチル共重合体等が挙げられる。
本発明はまた、本発明の間欠的持久力向上剤および/または本発明の血中pH上昇剤を含む、飲食品(以下、「本発明の飲食品」と称することがある)を提供する。
6週齢のC57BL/6J雄性マウスに被験物質を摂取させた後、マウスYO−YOテストを実施し、各個体の間欠的持久力を指標として被験物質の間欠的持久力の向上効果を評価した。なお、被験物質としては、20種類のアミノ酸(またはその塩)を用いた。これらを単独投与または様々な組み合わせで併用投与し、いずれのアミノ酸またはその組み合わせが、間欠的持久力の向上効果を有するかについて検討した。さらに、アミノ酸とカフェインまたは糖質との併用や、これらの使用量の関係等についても、間欠的持久力の向上効果の観点から網羅的に検討した。
本試験の一週間前に、マウスに予備走行を実施した。トレッドミルの傾斜は20度、30秒間の歩行(速度5m/分)と、2分間の走行を1セットとし、セット数が上がるごとに走行スピードを12〜33m/分まで漸増させた。マウスが走行スピードについていけなくなった時点で走行不能と判断した。走行不能の状態を2セット連続で観察した時を本評価系からの脱落と判定し、その時点までに走行したセット数を各個体が持つ間欠的持久能力とした。予備走行で得られた各個体の走行セット数と体重が、各群で同程度となるように群分けを行った。
予備走行翌週に、間欠的持久力を判定したマウスに、1〜2g/kgマウス体重の用量の被験物質を含む水溶液、または水(ネガティブコントロール)を20mL/kgマウス体重で経口投与した。なお、間欠的持久力の向上効果が知られているカフェインをこの試験におけるポジティブコントロールとして用いた。当該経口投与の30分後から、前述したYO−YO試験を行い、被験物質による各個体の走行可能セット数への影響を評価した。間欠的持久力が向上したか否かの評価は、被験物質を摂取した時に確認した走行可能セット数から、予備走行時の走行可能セット数を差し引き、被験物質の摂取による走行可能セット数の増加を算出することにより行った。
7〜9週齢のC57BL/6J雄性マウスを用いて、1g/kgの用量のアスパラギン酸、または炭酸水素ナトリウム(ポジティブコントロール)を経口投与し、当該経口投与から30分後、60分後、120分後にイソフルラン麻酔下で採血した。得られた血液を遠心分離に供して血漿を採取し、i―STAT(abbott社製)を用いて、血中pHを測定した。
Claims (7)
- アスパラギン酸およびチロシンのいずれかまたは両方を含む、間欠的持久力向上剤。
- アスパラギン酸およびチロシンを含む、請求項1記載の剤。
- アスパラギン酸とチロシンの割合が、重量比において、アスパラギン酸:チロシン=1:0.1〜10である、請求項2記載の剤。
- アスパラギン酸を含む、血中pH上昇剤。
- アシドーシス改善に用いられることを特徴とする、請求項4記載の剤。
- 以下からなる群から選択される1以上の疾患の治療、改善、または予防に用いられることを特徴とする、請求項4または5記載の剤:
(1)高尿酸血症
(2)痛風。 - 請求項1〜6のいずれか一項に記載の剤を含む、飲食品。
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