JP6053695B2 - 食欲抑制剤 - Google Patents
食欲抑制剤 Download PDFInfo
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- JP6053695B2 JP6053695B2 JP2013554179A JP2013554179A JP6053695B2 JP 6053695 B2 JP6053695 B2 JP 6053695B2 JP 2013554179 A JP2013554179 A JP 2013554179A JP 2013554179 A JP2013554179 A JP 2013554179A JP 6053695 B2 JP6053695 B2 JP 6053695B2
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- acid
- palmitoleic acid
- administration
- palmitoleic
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Description
(1)パルミトレイン酸、その塩およびそのエステルから選択される成分を有効成分として含有する、食欲抑制剤。
(2)パルミトレイン酸C1−6アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択されるパルミトレイン酸エステルを有効成分として含有する、上記(1)に記載の食欲抑制剤。
(3)パルミトレイン酸エチルエステルを有効成分として含有する、上記(1)に記載の食欲抑制剤。
(4)パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを有効成分として含有する、上記(1)に記載の食欲抑制剤。
(5)トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、上記(4)に記載の食欲抑制剤。
(6)パルミトレイン酸、その塩およびそのエステルから選択される成分を有効成分として含有する、摂食障害または肥満の治療または予防に使用するための医薬組成物。
(7)パルミトレイン酸C1−6アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択されるパルミトレイン酸エステルを有効成分として含有する、上記(6)に記載の医薬組成物。
(8)パルミトレイン酸エチルエステルを有効成分として含有する、上記(6)に記載の医薬組成物。
(9)パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを有効成分として含有する、上記(6)に記載の医薬組成物。
(10)トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、上記(9)に記載の医薬組成物。
(11)治療有効量のパルミトレイン酸、その塩またはそのエステルを対象に投与することを含む、摂食障害または肥満の方法。
(12)パルミトレイン酸C1−6アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択されるパルミトレイン酸エステルを投与する、上記(11)に記載の方法。
(13)パルミトレイン酸エチルエステルを投与する、上記(11)に記載の方法。
(14)パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを投与する、上記(11)に記載の方法。
(15)トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、上記(14)に記載の方法。
(16)有効量のパルミトレイン酸、その塩またはそのエステルを対象に投与することを含む、対象の摂食量の抑制方法。
(17)パルミトレイン酸C1−6アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択されるパルミトレイン酸エステルを投与する、上記(16)に記載の方法。
(18)パルミトレイン酸エチルエステルを投与する、上記(16)に記載の方法。
(19)パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを投与する、上記(16)に記載の方法。
(20)トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、上記(19)に記載の方法。
(21)有効量のパルミトレイン酸、その塩またはそのエステルを食前に対象に投与することを含む、上記(16)〜(19)のいずれかに記載の方法。
(22)パルミトレイン酸、その塩およびそのエステルから選択される成分を含有する飲食品。
(23)パルミトレイン酸C1−6アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択されるパルミトレイン酸エステルを有効成分として含有する、上記(22)に記載の飲食品。
(24)パルミトレイン酸エチルエステルを有効成分として含有する、上記(22)に記載の飲食品。
(25)パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを有効成分として含有する、上記(22)に記載の飲食品。
(26)トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、上記(25)に記載の飲食品。
(27)肥満症または摂食障害の患者用の飲食品として使用される、上記(22)〜(26)のいずれかに記載の飲食品。
(28)肥満症または摂食障害の予防用の飲食品として使用される、上記(22)〜(26)のいずれかに記載の飲食品。
(29)パルミトレイン酸、その塩およびそのエステルから選択される成分を0.01〜99重量%含む、上記(22)〜(28)のいずれかに記載の飲食品。
(1)投与試料の調製
グリセリン脂肪酸エステル(リョートー(登録商標)ポリグリエステル、三菱化学フーズ株式会社)の1.5%水溶液(重量比)を溶媒とし、パルミトレイン酸の遊離脂肪酸(C16:1)、パルミチン酸の遊離脂肪酸(C16:0)、ガドレイン酸の遊離脂肪酸(C20:1)、およびエルカ酸の遊離脂肪酸(C22:1)(いずれもシグマ社製、純度99%以上であるもの)をこの溶媒に加えてアイスバス中で超音波処理して均一乳化させ、投与試料とした。
(2)糖尿病モデル動物
雄性の自然発症糖尿病モデルマウスKKAy/Ta(以下、KKAyマウス)を試験に使用した。5週齢KKAyマウス(日本クレア株式会社)を購入し、個別ケージにて1週間の予備飼育を行った。予備飼育期間中は、固形飼料ラボMRストック(日本農産工業株式会社)及び蒸留水を給水瓶にて自由摂取させた。
(3)KKAyマウスを用いた本試験
予備飼育後6週齢のKKAyマウスを、溶媒のみを投与する対照群(以下、対照群)、パルミトレイン酸(C16:1)を投与する群(以下、C16:1投与群)、パルミチン酸(C16:0)を投与する群(以下、C16:0投与群)、ガドレイン酸(C20:1)を投与する群(以下、C20:1投与群)、およびエルカ酸(C22:1)を投与する群(以下、C22:1投与群)に体重を考慮して分け(1群10匹)、これを本試験に供した。本試験では、これら各群のマウスを12時間毎の明暗サイクルの環境下で、粉末飼料ラボMRストック(日本農産工業株式会社)及び蒸留水を給水瓶にて自由摂取させて4週間飼育した。その間、溶媒または各脂肪酸を、胃ゾンデを用いて毎日10時に経口投与した。このうち、対照群には溶媒をKKAyマウス1匹あたり10mL/kgの投与量で経口投与した。また、試験対象物であるC16:1, C16:0, C20:1およびC22:1は、300mgを溶媒10mLに加え乳化し、KKAyマウス1匹あたり10mL/kgの投与量で経口投与した。
(4)KKAyマウスの摂餌量および体重測定
4週間の飼育期間中に、投与1、5、9、12、16、19、23および26日に給餌量を、翌日に残量を給餌器ごと測定し、連続した2回の測定値の差から1日あたりの摂餌量を算出した。平均摂餌量は各測定日に測定した摂餌量の平均値である。また、投与開始日(Pre)、および投与1、2,3、および4週間後体重測定を行った。体重増加率は[(終体重−始体重)/始体重]×100によって算出した。なお、終体重は4週間の飼育期間が終了した後測定した体重であり、始体重は試験開始時に測定した体重である。
(5)摂餌量および体重変化の結果
対照群と比べ、C16:1投与群の摂餌量は有意に低下した(図1および2)。体重の変化において、対照群と比べ、C16:1投与群における体重は投与2週目から4週目にかけ有意に低下した(図3)。また、対照群と比べ、C16:1投与群における体重増加率も有意に低下した(図4)。一方、他の脂肪酸投与群においては摂餌量および体重のわずかな低下傾向が認められたものの、有意性は認められなかった。
(1)投与試料の調製
グリセリン脂肪酸エステル(リョートー(登録商標)ポリグリエステル、三菱化学フーズ株式会社)の1.5%水溶液(重量比)を溶媒として、パルミトレイン酸の遊離脂肪酸(C16:1)、パルミチン酸の遊離脂肪酸(C16:0)、オレイン酸の遊離脂肪酸(C18:1)、ラウリン酸の遊離脂肪酸(C12:0)、デセン酸の遊離脂肪酸(C10:1)、リノール酸の遊離脂肪酸(C18:2)(いずれもシグマ社製)をこの溶媒に加えてアイスバス中で超音波処理して均一乳化させ、投与試料とした。
(2)実験動物
雄性のSprague-Dawleyラット(以下、SDラット)を実験に使用した。9週齢SDラット(日本エスエルシー株式会社)を購入し、個別ケージにて1週間の予備飼育を行った。予備飼育期間中は、固形飼料ラボMRストック(日本農産工業株式会社)及び蒸留水を給水瓶にて自由摂取させた。
(3)SDラットを用いた本試験
予備飼育後10週齢のSDラットを、溶媒のみを投与する対照群(以下、対照群)、パルミトレイン酸(C16:1)を投与する群(以下、C16:1投与群)、パルミチン酸(C16:0)を投与する群(以下、C16:0投与群)、オレイン酸(C18:1)を投与する群(以下、C18:1投与群)、ラウリン酸(C12:0)を投与する群(以下、C12:0投与群)、デセン酸(C10:1)を投与する群(以下、C10:1投与群)、リノール酸(C18:2)を投与する群(以下、C18:2投与群)に体重を考慮して分け(1群10匹)、これを本試験に供した。本試験では、溶媒または各脂肪酸を、胃ゾンデを用いて実験当日に単回経口投与した。このうち、対照群には溶媒をSDラット1匹あたり10mL/kgの投与量で経口投与した。また、試験対象物であるC16:1、C16:0、C18:1、C12:0、C10:1、またはC18:2は、それぞれ150mgまたは500mgを溶媒10mLに加え乳化し、SDラット1匹あたり10mL/kgの投与量で経口投与して30分間後または1時間後測定した。摂餌量(サンプル投与直後の餌量からサンプル投与所定時間後の餌量を引いたもの)は、試験サンプルを経口投与して30分間後または1時間後測定した。
(4)パルミトレイン酸(遊離脂肪酸)単回経口投与の摂餌量への影響
被験物質投与30分間および1時間後、対照群およびC16:0投与群と比べ、C16:1投与群における摂餌量は有意に低下した(図5および6)。なお、C16:1の濃度依存性実験では、被験物質投与30分間後、対照群およびC16:0投与群と比べ、C16:1投与群における摂餌量はC16:1の濃度依存的に有意に低下した(図7)。また、同じ一価不飽和脂肪酸であるC18:1との比較試験では、被験物質投与30分間および1時間後、対照群およびC18:1投与群と比べ、C16:1投与群における摂餌量は有意に低下した(図8〜10)。さらに、他の短鎖飽和脂肪酸(C12:0)、短鎖一価不飽和脂肪酸(C10:1)および長鎖多価不飽和脂肪酸(C18:2)との比較試験では、被験物質投与1時間後、対照群と比べ、C16:1投与群における摂餌量は有意に低下したが、C12:0投与群、C10:1投与群および C18:2投与群における摂餌量には有意な低下が無かった(図11)。
(1)投与試料の調製
グリセリン脂肪酸エステル(リョートー(登録商標)ポリグリエステル、三菱化学フーズ株式会社)の1.5%水溶液(重量比)を溶媒として、パルミトレイン酸(C16:1)のトリグリセリド濃縮油(交洋ファイケミカル株式会社製)およびオリーブ油(シグマ社製、純度99%以上であるもの)をこの溶媒に加えてアイスバス中で超音波処理して均一乳化させ、投与試料とした。パルミトレイン酸濃縮油およびオリーブ油の主な脂肪酸組成は表1に示した。
雄性のSprague-Dawleyラット(以下、SDラット)を用いて試験を行った。9週齢SDラット(日本エスエルシー株式会社)を購入し、個別ケージにて1週間の予備飼育を行った。予備飼育期間中は、固形飼料ラボMRストック(日本農産工業株式会社)及び蒸留水を給水瓶にて自由摂取させた。
(3)SDラットを用いた本試験
予備飼育後10週齢のSDラットを、溶媒のみを投与する対照群(以下、対照群)、パルミトレイン酸(C16:1)のトリグリセリド濃縮油を投与する群(以下、C16:1濃縮油投与群)、およびオリーブ油を投与する群(以下、オリーブ油投与群)に体重を考慮して分け(1群10匹)、これを本試験に供した。本試験では、溶媒または各油脂を、胃ゾンデを用いて実験当日に単回経口投与した。このうち、対照群には溶媒をSDラット1匹あたり10mL/kgの投与量で経口投与した。また、試験対象物であるC16:1濃縮油に含有されるC16:1が150mg/kgまたは500mg/kgになるようにC16:1濃縮油を経口投与し、オリーブ油に含有されるC18:1が150mg/kgまたは500mg/kgになるようにオリーブ油を経口投与した。摂餌量(サンプル投与直後の餌量からサンプル投与所定時間後の餌量を引いたもの)は、試験サンプルを経口投与して1時間後測定した。
(4)パルミトレイン酸トリグリセリド濃縮油単回経口投与の摂餌量への影響
被験物質投与1時間後、対照群と比べ、パルミトレイン酸濃縮油投与群(パルミトレイン酸の相当量:500mg/kg)における摂餌量は有意に低下した。一方、オリーブ油投与群には有意な摂餌量の低下は見られなかった(図12)。
(1)投与試料の調製
グリセリン脂肪酸エステル(リョートー(登録商標)ポリグリエステル、三菱化学フーズ株式会社)の1.5%水溶液(重量比)を溶媒として、パルミトレイン酸の遊離脂肪酸 (C16:1)またはオレイン酸の遊離脂肪酸(C18:1) (いずれもシグマ社製)をこの溶媒に加えてアイスバス中で超音波処理して均一乳化させ、投与試料とした。
(2)実験動物
雄性のSprague-Dawleyラット(以下、SDラット)を用いて試験を行った。9週齢SDラット(日本エスエルシー株式会社)を購入し、個別ケージにて1週間の予備飼育を行った。予備飼育期間中は、固形飼料ラボMRストック(日本農産工業株式会社)及び蒸留水を給水瓶にて自由摂取させた。
(3)SDラットを用いた本試験
予備飼育後10週齢のSDラットを、溶媒のみを投与する対照群(以下、対照群)、パルミトレイン酸(C16:1)を投与する群(以下、C16:1投与群)およびオレイン酸(C18:1)を投与する群(以下、C18:1投与群)に体重を考慮して分け(1群10匹)、これを本試験に供した。本試験では、溶媒または各脂肪酸を、胃ゾンデを用いて実験当日に単回経口投与した。このうち、対照群の溶媒をSDラット1匹あたり10mL/kgの投与量で経口投与した。また、試験対象物であるパルミトレイン酸またはオレイン酸は、それぞれ150mgまたは500mgを溶媒10mLに加え乳化し、SDラット1匹あたり10mL/kg経口投与して1時間後、4%ペントバルビタール麻酔下で腹大動脈からヘパリン存在下で全採血し、放血致死させた。血液は、遠心機 (CF8DL、日立工機株式会社) を用いて遠心分離 (4℃、3000rpm (約1972g)、15分間) し、得られた血漿を血中コレシストニン(CCK)濃度測定するまで凍結保存した。CCKの血中濃度を酵素免疫測定法(ELISA)キット(Cholecystokinin (CCK) EIA Kit, Phoenix Pharmaceuticals, Inc.)によって測定した。さらに、CCKのメッセンジャーRNA(mRNA)発現量の測定は、小腸から抽出した全RNAについて合成したcDNAを用いて、リアルタイムPCR反応を行うことによって評価した。内在性の対照遺伝子として18sリボソームRNA遺伝子を用いた。対照群における遺伝子の発現量を1として、C16:1投与群またはC18:1投与群における各遺伝子の相対発現量を算出した。なお、CCK遺伝子におけるプライマーは以下の通りである。
F 5′-CATCCAGCAGGTCCGCAAA-3′, R 5′-TCCATCCAGCCCATGTAGTCC-3′.
(4)結果
被験物質投与1時間後、対象群と比べて、C16:1投与群(500mg/kg)における血中CCK濃度および小腸中CCKのmRNA発現量は有意に増加したが、オレイン酸投与群には血中CCK濃度の有意な上昇は見られなかった(図13および14)。
Claims (5)
- パルミトレイン酸、その塩、パルミトレイン酸C 1−6 アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択される成分を有効成分として含有する、食欲抑制剤であって、1日あたり150〜500mg/kgのパルミトレイン酸が対象に摂取されるように用いられることを特徴とする、前記食欲抑制剤。
- パルミトレイン酸エチルエステルを有効成分として含有する、請求項1に記載の食欲抑制剤。
- パルミトレイン酸を構成脂肪酸として含有するトリグリセリドを有効成分として含有する、請求項1に記載の食欲抑制剤。
- トリグリセリドの脂肪酸組成においてパルミトレイン酸が30%以上である、請求項3に記載の食欲抑制剤。
- パルミトレイン酸、その塩、パルミトレイン酸C 1−6 アルキルエステルおよびパルミトレイン酸を構成脂肪酸として含有するグリセリドから選択される成分を有効成分として含有する、摂食障害または肥満の治療または予防に使用するための医薬組成物であって、1日あたり150〜500mg/kgのパルミトレイン酸が対象に摂取されるように用いられることを特徴とする、前記医薬組成物。
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