Raddad Eyas, Chappell Amy, Meyer Jeffery, Wilson Alan, Ruegg Charles E, Tauscher Johannes, Statnick Michael A, Barth Vanessa, Zhang Xin, Verfaille Steven J
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana (E.R., A.C., C.E.R., J.T., M.A.S., V.B., X.Z., S.J.V.); Research Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada (J.M., A.W.)
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana (E.R., A.C., C.E.R., J.T., M.A.S., V.B., X.Z., S.J.V.); Research Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada (J.M., A.W.).
Drug Metab Dispos. 2016 Sep;44(9):1536-42. doi: 10.1124/dmd.116.070359. Epub 2016 Jun 27.
Therapeutic benefits from nociceptin opioid peptide receptor (NOP) antagonism were proposed for obesity, eating disorders, and depression. LY2940094 ([2-[4-[(2-chloro-4,4-difluoro-spiro[5H-thieno[2,3-c]pyran-7,4'-piperidine]-1'-yl)methyl]-3-methyl-pyrazol-1-yl]-3-pyridyl]methanol) is a novel, orally bioavailable, potent, and selective NOP antagonist. We studied NOP receptor occupancy (RO) after single oral LY2940094 doses in rat hypothalamus and human brain by use of liquid chromatography with tandem mass spectrometry (LC-MS/MS) (LSN2810397) and positron emission tomography (PET) ([(11)C]NOP-1A) tracers, respectively. A bolus plus constant infusion tracer protocol with PET was employed in humans at 2.5 and 26.5 hours after administration of the LY2940094 dose. The RO was calculated from the change in regional distributional volume (VT) corrected for nondisplaceable volume using Lasson plots. The RO followed a simple Emax relationship to plasma LY2940094 concentration, reaching near complete occupancy in both species. For rat hypothalamus, the plasma concentration at half-maximum RO (EC50) was 5.8 ng/ml. In humans, LY2940094 was well tolerated and safe over the 4-40 mg dose range, and it peaked in plasma at 2 to 6 hours after a 1- to 2-hour lag, with approximate dose-proportional exposure. After 4-40 mg doses, NOP RO was similar across the prefrontal cortex, occipital cortex, putamen, and thalamus, with EC50 of 2.94 to 3.46 ng/ml, less than 2-fold lower than in rats. Over 4-40 mg doses, LY2940094 mean plasma levels at peak and 24 hours were 7.93-102 and 1.17-14.1 ng/ml, corresponding to the cross-region average NOP RO of 73%-97% and 28%-82%, respectively. The rat EC50 translates well to humans. LY2940094 readily penetrates the human brain, and a once-daily oral dose of 40 mg achieves sustainably high (>80%) NOP RO levels suitable for testing clinical efficacy.
人们提出,伤害感受素阿片肽受体(NOP)拮抗剂对肥胖症、饮食失调和抑郁症具有治疗作用。LY2940094([2-[4-[(2-氯-4,4-二氟-螺[5H-噻吩并[2,3-c]吡喃-7,4'-哌啶]-1'-基)甲基]-3-甲基-吡唑-1-基]-3-吡啶基]甲醇)是一种新型的、口服生物可利用的、强效且选择性的NOP拮抗剂。我们分别通过液相色谱-串联质谱法(LC-MS/MS)(LSN2810397)和正电子发射断层扫描(PET)([(11)C]NOP-1A)示踪剂,研究了大鼠下丘脑和人脑中单次口服LY2940094剂量后的NOP受体占有率(RO)。在给予LY2940094剂量后的2.5小时和26.5小时,对人体采用了PET的推注加持续输注示踪剂方案。RO是根据使用拉森图校正了不可置换体积后的区域分布体积(VT)变化来计算的。RO与血浆LY2940094浓度呈简单的Emax关系,在两个物种中均达到接近完全占有率。对于大鼠下丘脑,RO达到半数最大值时的血浆浓度(EC50)为5.8 ng/ml。在人体中,LY2940094在4 - 40 mg剂量范围内耐受性良好且安全,在1 - 2小时的延迟后,血浆浓度在2至6小时达到峰值,暴露量大致与剂量成比例。给予4 - 4 mg剂量后,前额叶皮质、枕叶皮质、壳核和丘脑中的NOP RO相似,EC50为2.94至3.46 ng/ml,比大鼠低不到2倍。在4 - 40 mg剂量范围内,LY2940094在峰值和24小时时的平均血浆水平分别为7.93 - 102 ng/ml和1.ll - 14.1 ng/ml,分别对应跨区域平均NOP RO为73% - 97%和28% - 82%。大鼠的EC50能很好地类推到人体。LY2940094能轻易穿透人脑,每日口服40 mg的剂量可持续达到较高(>80%)的NOP RO水平,适合测试临床疗效。