Sanhouri A A, Jones R S, Dobson H
Department of Veterinary Clinical Science, University of Liverpool, Neston, South Wirral.
Br Vet J. 1991 Jan-Feb;147(1):42-8. doi: 10.1016/0007-1935(91)90065-U.
Pentobarbitone (20 mg/kg i.v.) blocked plasma cortisol release when administered either before a 20 min journey or during a 2 h journey. This confirms that pentobarbitone can block stimulated, as well as resting, cortisol secretion. In general, blood glucose concentrations were not increased above 90 mg/100 ml until at least 30 min after the start of transport; however, this increase was also blocked by pentobarbitone administered 30 min into the 2 h journey. Significant increases in respiratory and heart rates occurred within 15 min of the start of transport; pentobarbitone caused an immediate decrease in these parameters. In conclusion, pentobarbitone was shown to reverse many metabolic changes induced by transport.
静脉注射戊巴比妥钠(20毫克/千克),无论是在20分钟行程前给药还是在2小时行程中给药,均能抑制血浆皮质醇的释放。这证实了戊巴比妥钠既能抑制静息状态下的皮质醇分泌,也能抑制刺激状态下的皮质醇分泌。一般来说,直到运输开始至少30分钟后,血糖浓度才会升高到90毫克/100毫升以上;然而,在2小时行程开始30分钟时注射戊巴比妥钠也能抑制这种升高。运输开始后15分钟内,呼吸和心率显著增加;戊巴比妥钠使这些参数立即下降。总之,戊巴比妥钠被证明可以逆转运输引起的许多代谢变化。