JP2016518367A - 虚血性損傷の治療及び予防用の組成物 - Google Patents
虚血性損傷の治療及び予防用の組成物 Download PDFInfo
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- JP2016518367A JP2016518367A JP2016508901A JP2016508901A JP2016518367A JP 2016518367 A JP2016518367 A JP 2016518367A JP 2016508901 A JP2016508901 A JP 2016508901A JP 2016508901 A JP2016508901 A JP 2016508901A JP 2016518367 A JP2016518367 A JP 2016518367A
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Abstract
Description
(1)疎水性:ノルロイシン、met、ala、val、leu、ile;
(2)中性親水性:cys、ser、thr;
(3)酸性:asp、glu;
(4)塩基性:asn、gln、his、lys、arg;
(5)鎖配向に影響を及ぼす残基:gly、pro;及び
(6)芳香族:trp、tyr、phe。
配列番号1のペプチド(以下「PEP 1」とする)を従来に知られた固相ペプチド合成法(SPPS:solid phase peptide synthesis)によって製造した。具体的には、ペプチドは、ASP48S(Peptron、Inc.,大韓民国・大田)を利用して、Fmoc固相合成法を介して、C末端からアミノ酸一つずつカップリングすることによって合成した。次のように、ペプチドのC末端の最初のアミノ酸が樹脂に付着されたものを使用した。例えば、次の通りである:
NH2−Lys(Boc)−2−クロロ−トリチルレジン
NH2−Ala−2−クロロ−トリチルレジン
NH2−Arg(Pbf)−2−クロロ−トリチルレジン
Fmoc−Ala−OH、Fmoc−Arg(Pbf)−OH、Fmoc−Glu(OtBu)−OH、Fmoc−Pro−OH、Fmoc−Leu−OH、Fmoc−Ile−OH、Fmoc−Phe−OH、Fmoc−Ser(tBu)−OH、Fmoc−Thr(tBu)−OH、Fmoc−Lys(Boc)−OH、Fmoc−Gln(Trt)−OH、Fmoc−Trp(Boc)−OH、Fmoc−Met−OH、Fmoc−Asn(Trt)−OH、Fmoc−Tyr(tBu)−OH、Fmoc−Ahx−OH、Trt−メルカプト酢酸。
1)カップリング
NH2−Lys(Boc)−2−クロロ−トリチルレジンで保護されたアミノ酸(8当量)と、カップリング試薬HBTU(8当量)/HOBt(8当量)/NMM(16当量)とをDMFに溶解させて添加した後、常温で2時間反応させ、DMF、MeOH、DMFの順に洗浄した。
2)Fmoc脱保護
20%のDMF中のピペリジン(DMF中)を加え、常温で5分間2回反応させ、DMF、MeOH、DMFの順に洗浄した。
3)1及び2の反応を反復して行い、ペプチド基本骨格NH2−E(OtBu)−A−R(Pbf)−P−A−L−L−T(tBu)−S(tBu)−R(Pbf)L−R(Pbf)−F−I−P−K(Boc)−2−クロロ−トリチルレジン)を作った。
4)切断:合成が完了したペプチドResinに、切断カクテルを加え、ペプチドをResinから分離した。
5)得られた混合物に、冷却したジエチルエーテルを加えた後、遠心分離して得られたペプチドを沈澱させる。
6)Prep−HPLCで精製した後、LC/MSで分子量を確認して凍結させ、パウダーに製造した。
試験例1:虚血再灌流の誘導
腎臓虚血再灌流損傷のあるマウスモデルは、腎臓肉茎に30分間、両側クランピング(bilateral clamping)を行い、30分後にクランプを除去して血液の流れを復元させる方法で虚血再灌流を誘導して得た。実験群は、投与群(PEP1)、対照群(PBS:PEP1投与せず)、そしてSham(両側クランピングなし)の3グループに分類した。PEP1は、1,000nmol/kg濃度で、虚血再灌流誘導の30分前及び12時間後に皮下注射した。
虚血再灌流24時間後に血液を採取し、腎臓毒性指標である血中尿素窒素(BUN)、クレアチンを測定し、腎臓組織は摘出し、パラフィンブロックを製作し、免疫組織化学検査及び組織学的検査を進め、タンパク質を抽出してサイトカインレベルを測定した。クレアチン濃度とBUNは、自動分析機(Technicon RA−1000;Bayer,Tarrytown,NY)を利用して測定した。
虚血再灌流24時間後、腎臓組織をPAS(過ヨウ素酸−シッフ)染色(製造社:Polysciences株式会社(ウォリントン、PA、米国))プロトコルによって、PASキットでPAS染色)を行った。染色を行った後、腎臓組織損傷スコアリングで腎組織損傷を評価した。PEP1の投与群は、PBS対照群に比べ、腎臓組織の損傷が著しく緩和された様相を示した(図2及び図3)。
虚血再灌流24時間後、腎臓組織に対して、TUNEL染色で腎臓組織細胞死滅を評価した。ロシュ応用科学(インディアナポリス、IN、米国)で作ったTUNEL染色キットを介して、パラフィン腎臓セクションにTUNEL染色を行った。
虚血再灌流24時間後、腎臓組織に対して、F4/80(マクロファージマーカー)、Gr−1(好中球マーカー)の免疫組織染色で、先天免疫細胞浸潤を評価した。具体的には、大食細胞に特異的な抗体(F4/80、abcam、Cambridge、MA)を使用して、パラフィン含有セクション上の免疫化学的な方法で、大食細胞及び好中球細胞の浸透染色を行った。
虚血再灌流24時間後、腎臓組織からタンパク質を抽出し、サイトメトリックビードアレイ方法で、IL−6,MCP−1,TNF−αのレベルを測定した。マウスIL6、MCP−1、TNFa ElISAキットは、R&D Systemsから購入し、製造社のプロトコルによって実験を行った。
試験例1:虚血再灌流の誘導
虚血再灌流損傷のあるラットモデルは、白マウス(Sprague−Dawley Rat、180gから230g)の腹の皮膚に5cm×5cmサイズで皮弁を採取した後、PEP1または生理食塩水を投与し、クランピングを行い、虚血を起こさせ、7時間後にクランプを除去し、血液の流れを復元させる方法で虚血再灌流損傷を誘導して得た(図11参照)。
虚血再灌流を誘導した後7日後に、皮弁生存率(flap survivability)を測定した。皮弁生存率の測定は、ImageJプログラムを介したデジタル写真分析を介して行った。
Claims (13)
- 配列番号1のアミノ酸配列を含むペプチド、前記アミノ酸配列と80%以上の配列相同性を有するペプチド、またはその断片であるペプチドを含む虚血性損傷の治療及び予防用の組成物。
- 前記断片は、3個以上のアミノ酸から構成された断片であることを特徴とする請求項1に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血性損傷は、虚血再灌流損傷、血管疾病、冠状動脈血栓症、脳血管血栓症、動脈瘤破裂、全身出血、圧潰損傷、敗血症、皮膚火傷、血管閉塞性手術法、心肺迂路法、臓器移植、心肺虚脱(急性心臓死)及び窒息からなる群から選択される1以上の原因によることを特徴とする請求項1に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血性損傷は、虚血再灌流損傷によることを特徴とする請求項3に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血再灌流損傷は、脳血管虚血再灌流損傷、腎臓虚血再灌流損傷、肝臓虚血再灌流損傷、虚血再灌流心筋病症、皮膚虚血再灌流損傷、腸管虚血再灌流損傷、腸虚血再灌流損傷、胃虚血再灌流損傷、肺虚血再灌流損傷、膵臓虚血再灌流損傷、骨格筋虚血再灌流損傷、腹筋虚血再灌流損傷、四肢虚血再灌流損傷、虚血再灌流結腸炎、腸間膜虚血再灌流損傷及び無症侯性虚血再灌流損傷からなる群から選択されることを特徴とする請求項4に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血再灌流損傷は、臓器移植によることを特徴とする請求項4に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血再灌流損傷は、腎臓で起こることを特徴とする請求項4に記載の虚血性損傷の治療及び予防用の組成物。
- 前記虚血再灌流損傷は、皮弁で起こることを特徴とする請求項4に記載の虚血性損傷の治療及び予防用の組成物。
- 前記組成物は、皮弁生存率向上のためのものであることを特徴とする請求項8に記載の虚血性損傷の治療及び予防用の組成物。
- 前記ペプチドは、ヒトテロメラーゼに由来したことを特徴とする請求項1に記載の虚血性損傷の治療及び予防用の組成物。
- 前記組成物は、薬学組成物であることを特徴とする請求項1に記載の虚血性損傷の治療及び予防用の組成物。
- 前記組成物は、食品組成物であることを特徴とする請求項1に記載の虚血性損傷の治療及び予防用の組成物。
- 請求項1ないし12のうちいずれか1項に記載の組成物を、治療を必要とする対象に投与することを特徴とする虚血性損傷を治療及び予防する方法。
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KR102258864B1 (ko) | 2021-06-01 |
TWI653980B (zh) | 2019-03-21 |
KR20160008165A (ko) | 2016-01-21 |
EP2987497B1 (en) | 2018-12-26 |
EP2987497A1 (en) | 2016-02-24 |
US9907838B2 (en) | 2018-03-06 |
CN105263508B (zh) | 2019-10-25 |
CN105263508A (zh) | 2016-01-20 |
JP6474786B2 (ja) | 2019-02-27 |
US20160082089A1 (en) | 2016-03-24 |
WO2014171792A1 (ko) | 2014-10-23 |
ES2716870T3 (es) | 2019-06-17 |
TW201521763A (zh) | 2015-06-16 |
EP2987497A4 (en) | 2016-11-09 |
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