Effect of phosphoramidon - a selective enkephalinase inhibitor - on nociception and behaviour

Phosphoramidon (100-350 micrograms i.c.v.), a selective enkephalinase inhibitor, induced in the rat a decrease of nociception to pressure stimulation without evident respiratory depression. In addition, intensive behavioural changes such as grooming (licking the fur, face washing and scratching), mounting behaviour and wet dog shakes were observed. Naltrexone pretreatment (1 mg/kg i.p.) caused a significant decrease in the phosphoramidon-induced nociception and behavioural changes. Puromycin (30 micrograms i.c.v. or 7.5 mg/kg i.p.) caused no changes in nociception or behaviour.     

Anti-nociceptive and anti-inflammatory effects of the ethanolic extract of potato (Solanum tuberlosum)

The ethanol extract of potato tubers (Solanum tuberlosum L.) has been evaluated for antinociceptive and anti-inflammatory activities in mice. The acute treatment of mice with an ethanolic extract from the potato tuber at doses of 100 and 200 mg/kg, by oral administration, produced a significant anti-nociceptive effect in the acetic acid-induced writhing, formalin-induced pain licking and hot plate-induced pain. Also, the ethanolic extract of potato tubers significantly inhibited both carrageenan- and formalin-induced inflammation in mice as well as arachidonic acid-induced ear edema in mice. These inhibitions were statistically significant (p<0.05). These results provide support for the use of the ethanol extract of potato tuber in relieving inflammatory pain, and insight into the development of new agents for treating inflammatory diseases.     

Effect of GABA-ergic agents on the analgesic effect of morphine in rats

In order to detect possible interaction between GABA and opiates, the effects of GABA-ergic drugs on analgesia induced by morphine were studied. The vocalization response to electrical stimulation of the tail in rats was used as an index of the action of morphine. Thiosemicarbazide, an inhibitor of glutamate decarboxylase, and bicuculline, which blocks GABA-ergic receptors, drugs which, it is suggested, can be considered as a group of GABA-negative compounds, weaken and shorten the effect of morphine. Depakine, an inhibitor of -ketoglutarate-GABA-transaminase, like GABA itself, given in large doses (GABA-positive effects) strengthens morphine analgesia and prolongs its effect. The possible causes of these relations between GABA and opiates are discussed.Laboratory of Pharmacology of the Nervous System, Institute of Pharmacology, Academy of Medical Sciences of the USSR, Moscow. (Presented by Academician of the Academy of Medical Sciences of the USSR V. V. Zakusov.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 88, No. 7, pp. 35–37, July, 1979.     

不同镇痛方式在开胸术后的镇痛效果及对肺功能影响

目的观察不同镇痛方式在开胸手术后的镇痛效果及其对肺功能的影响。方法39例ASAⅠ~Ⅱ级,在硬膜外复合全身麻醉下行侧开胸手术的病人,术后随机接受罗哌卡因(罗哌组,n=10)、甲磺酸罗哌卡因(甲罗组,n=10)和布比卡因(布比组,n=10)硬膜外镇痛(patient controlled epidural analgesia,PCEA)及吗啡(吗啡组,n=9)静脉镇痛(patient controlled intravenous analgesia,PCIA)。结果术后1、2、5d静息时的疼痛评分罗哌组和甲罗组均明显低于布比组,但与吗啡组相比无明显差异;术后1d静息时疼痛评分吗啡组也明显低于布比组,但术后2、5d两组间无明显差异。术后1、2、5d咳嗽时疼痛评分罗哌组均明显低于布比组和吗啡组;各时间咳嗽时疼痛评分布比组和吗啡组之间无明显差异。术后1、2dPaCO2罗哌组均明显低于布比组,术后1dPaCO2罗哌组也明显低于布比组;术后1、2dPaCO2罗哌组均明显高于吗啡组,但与布比组之间无明显差异。术后1、2、5d用力肺活量和呼吸峰流速四组间无明显差异。结论罗哌卡因和甲磺酸罗哌卡因加舒芬太尼可安全用于开胸手术后硬膜外镇痛,其镇痛效果优于布比卡因加芬太尼硬膜外镇痛和吗啡静脉镇痛,并使术后病人维持更好的呼吸功能,且不增加副作用的发生率。