Villetti Gino, Carnini Chiara, Battipaglia Loredana, Preynat Laurent, Bolzoni Pier Tonino, Bassani Franco, Caruso Paola, Bergamaschi Marco, Pisano Anna Rita, Puviani Veronica, Stellari Fabio Franco, Cenacchi Valentina, Volta Roberta, Bertacche Vittorio, Mileo Valentina, Bagnacani Valentina, Moretti Elisa, Puccini Paola, Catinella Silvia, Facchinetti Fabrizio, Sala Angelo, Civelli Maurizio
Chiesi Farmaceutici S.p.A., Corporate Pre-Clinical R&D, Parma, Italy (G.V., C.C., L.B., L.P., P.T.B., F.B., P.C., M.B., A.R.P., V.P., F.F.S., V.C., R.V., Vi.B., V.M., Va.B., E.M., P.P, S.C., F.F., M.C.); Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy (A.S.); and Istituto di Biomedicina e Immunologia Molecolare, Consiglio Nazionale delle Ricerche, Palermo, Italy (A.S.)
Chiesi Farmaceutici S.p.A., Corporate Pre-Clinical R&D, Parma, Italy (G.V., C.C., L.B., L.P., P.T.B., F.B., P.C., M.B., A.R.P., V.P., F.F.S., V.C., R.V., Vi.B., V.M., Va.B., E.M., P.P, S.C., F.F., M.C.); Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy (A.S.); and Istituto di Biomedicina e Immunologia Molecolare, Consiglio Nazionale delle Ricerche, Palermo, Italy (A.S.).
J Pharmacol Exp Ther. 2015 Mar;352(3):568-78. doi: 10.1124/jpet.114.220558. Epub 2015 Jan 9.
CHF6001 [(S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyloxy)ethyl)pyridine 1-oxide] is a novel phosphodiesterase 4 (PDE4) inhibitor designed for use in pulmonary diseases by inhaled administration. Intratracheal administration of CHF6001 to ovalbumin-sensitized Brown-Norway rats suppressed the antigen-induced decline of lung functions (ED50 = 0.1 µmol/kg) and antigen-induced eosinophilia (ED50 = 0.03 µmol/kg) when administered (0.09 μmol/kg) up to 24 hours before antigen challenge, in agreement with CHF6001-sustained lung concentrations up to 72 hours after intratracheal treatment (mean residence time 26 hours). Intranasal, once daily administration of CHF6001 inhibited neutrophil infiltration observed after 11 days of tobacco smoke exposure in mice, both upon prophylactic (0.15-0.45 µmol/kg per day) or interventional (0.045-0.45 µmol/kg per day) treatment. CHF6001 was ineffective in reversing ketamine/xylazine-induced anesthesia (a surrogate of emesis in rat) up to 5 µmol/kg administered intratracheally, a dose 50- to 150-fold higher than anti-inflammatory ED50 observed in rats. When given topically to ferrets, no emesis and nausea were evident up to 10 to 20 µmol/kg, respectively, whereas the PDE4 inhibitor GSK-256066 (6-[3-(dimethylcarbamoyl)phenyl]sulfonyl-4-(3-methoxyanilino)-8-methylquinoline-3-carboxamide) induced nausea at 1 µmol/kg intratracheally. A 14-day inhalation toxicology study in rats showed a no-observed-adverse-effect level dose of 4.4 µmol/kg per day for CHF6001, lower than the 0.015 μmol/kg per day for GSK-256066. CHF6001 was found effective and extremely well tolerated upon topical administration in relevant animal models, and may represent a step forward in PDE4 inhibition for the treatment of asthma and chronic obstructive respiratory disease.
CHF6001 [(S)-3,5-二氯-4-(2-(3-(环丙基甲氧基)-4-(二氟甲氧基)苯基)-2-(3-(环丙基甲氧基)-4-(甲基磺酰胺基)苯甲酰氧基)乙基)吡啶1-氧化物]是一种新型磷酸二酯酶4(PDE4)抑制剂,设计用于通过吸入给药治疗肺部疾病。对卵清蛋白致敏的Brown-Norway大鼠气管内给予CHF6001,在抗原激发前24小时内给予(0.09 μmol/kg),可抑制抗原诱导的肺功能下降(ED50 = 0.1 μmol/kg)和抗原诱导的嗜酸性粒细胞增多(ED50 = 0.03 μmol/kg),这与气管内给药后长达72小时CHF6001在肺内持续存在的浓度一致(平均驻留时间26小时)。在小鼠中,每天经鼻给予CHF6001,在预防性(0.15 - 0.45 μmol/kg/天)或干预性(0.045 - 0.45 μmol/kg/天)治疗后,均可抑制烟草烟雾暴露11天后观察到的中性粒细胞浸润。气管内给予高达5 μmol/kg的CHF6001对氯胺酮/赛拉嗪诱导的麻醉(大鼠呕吐的替代指标)无效,该剂量比在大鼠中观察到的抗炎ED50高50至150倍。对雪貂局部给药时,分别给予高达10至20 μmol/kg时均未出现呕吐和恶心,而PDE4抑制剂GSK-256066 [6-[3-(二甲基氨基甲酰基)苯基]磺酰基-4-(3-甲氧基苯胺基)-8-甲基喹啉-3-甲酰胺]气管内给予1 μmol/kg时会引起恶心。对大鼠进行的为期14天的吸入毒理学研究表明,CHF6001的未观察到不良反应水平剂量为每天4.4 μmol/kg,低于GSK-256066的每天0.015 μmol/kg。在相关动物模型中,CHF6001经局部给药后被发现有效且耐受性极佳,可能代表了PDE4抑制在哮喘和慢性阻塞性呼吸道疾病治疗方面向前迈出的一步。