Sileno A P, Brandt G C, Spann B M, Quay S C
Nastech Pharmaceutical Company Inc., Bothell, WA 98021, USA.
Int J Obes (Lond). 2006 Jan;30(1):68-72. doi: 10.1038/sj.ijo.0803067.
Endogenous peptide YY(3-36) (PYY(3-36)) is associated with postprandial regulation of appetite. We investigated the safety and effectiveness of peripherally administered synthetic human PYY(3-36) for 14 days in New Zealand white rabbits. Weight gain and food consumption were assessed and pharmacokinetics and toxicity characterized.
In all, 24 animals were randomized to one of four intravenous treatment groups - control (0.9% saline) or PYY(3-36) bolus at 4.1, 41.0, or 205 microg/kg/day. Body weight and consumption of fixed food allotment were measured daily. Hematology and serum chemistries were profiled at baseline and Day 15, and pharmacokinetics measured following dose 14. Histopathologic examination of designated tissues and organs in control and PYY(3-36) 205 mug/kg animals was conducted. All animals were subject to clinical and macroscopic observation.
The trend effect of higher dose PYY(3-36) on lower average weight was significant (P = 0.01; Day 14 compared to baseline) and its effect on reduced food consumption was suggested (P = 0.065; number of days < or =75% food eaten, compared with control). Hematology and clinical chemistries were within normal limits pretest and at Day 15. No clinical, macroscopic, histologic, or microscopic changes related to the test article were observed over the course of study.
Lower average weight occurs in rabbits treated once daily with intravenous injection PYY(3-36) (205 microg/kg/day) over 14 days. No clinical or histologic signs of toxicity were observed. Further research is warranted to describe alternate routes of peripheral administration for optimizing weight control.
内源性肽YY(3-36)(PYY(3-36))与餐后食欲调节有关。我们研究了外周给予合成人PYY(3-36)14天对新西兰白兔的安全性和有效性。评估了体重增加和食物消耗情况,并对其药代动力学和毒性进行了表征。
总共24只动物被随机分为四个静脉治疗组之一——对照组(0.9%生理盐水)或分别以4.1、41.0或205微克/千克/天的剂量静脉推注PYY(3-36)。每天测量体重和固定食物配给量的消耗量。在基线和第15天进行血液学和血清化学分析,并在第14次给药后测量药代动力学。对对照组和给予205微克/千克PYY(3-36)的动物的指定组织和器官进行组织病理学检查。所有动物均接受临床和大体观察。
较高剂量的PYY(3-36)对较低平均体重的趋势效应显著(P = 0.01;与基线相比第14天),并且提示其对减少食物消耗有作用(P = 0.065;与对照组相比,进食量≤75%食物的天数)。血液学和临床化学指标在试验前和第15天均在正常范围内。在研究过程中未观察到与受试物相关的临床、大体、组织学或显微镜下变化。
在为期14天的时间里,每天一次静脉注射PYY(3-36)(205微克/千克/天)治疗的兔子平均体重降低。未观察到毒性的临床或组织学迹象。有必要进一步研究以描述外周给药的替代途径,以优化体重控制。