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叶下珠属选定物种愈伤组织培养提取物对小鼠的镇痛作用。

Analgesic effects of callus culture extracts from selected species of Phyllanthus in mice.

作者信息

Santos A R, Filho V C, Niero R, Viana A M, Moreno F N, Campos M M, Yunes R A, Calixto J B

机构信息

Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.

出版信息

J Pharm Pharmacol. 1994 Sep;46(9):755-9. doi: 10.1111/j.2042-7158.1994.tb03897.x.

Abstract

The aim of this study was to evaluate the analgesic effect of the methanolic extract from callus culture of Phyllanthus tenellus, P. corcovadensis and P. niruri in several models of pain in mice. The extracts (medium containing 2,4-dichlorophenoxyacetic acid) of P. corcovadensis, P. niruri and P. tenellus (3-90 mg kg-1, i.p.) caused graded inhibition of abdominal constrictions induced by acetic acid (0.6%), with ID50 (i.e. dose that reduced response of control by 50%) values of about 30, 19 and > 30 mg kg-1, respectively. The extract of callus of Phyllanthus obtained in indole-3-butyric acid and indole-3-acetic acid media (3-90 mg kg-1, i.p.) caused a similar analgesic effect. In the formalin test, the extract of P. tenellus obtained in indole butyric acid medium (3-100 mg kg-1, i.p.) inhibited only the second phase of formalin-induced pain with an ID50 value of about 100 mg kg-1. Both the indole acetic acid and indole butyric acid methanolic extracts of P. tenellus and P. corcovadensis (10-100 mg kg-1, i.p.) dose-dependently inhibited both phases of formalin-induced pain (ID50 values for the second phase were approx. 100 and 52 mg kg-1, respectively). However, the extract of callus from Phyllanthus failed to affect formalin-induced paw oedema, as well as the response to radiant heat in the tail-flick test. In addition, the analgesic effect of morphine, but not the analgesic effects caused by Phyllanthus callus extract, was fully antagonized by naloxone.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在评估叶下珠愈伤组织培养物甲醇提取物在几种小鼠疼痛模型中的镇痛作用。科科瓦多叶下珠、垂序商陆和叶下珠的提取物(含2,4-二氯苯氧乙酸的培养基)(3 - 90 mg kg-1,腹腔注射)对0.6%乙酸诱导的腹部收缩产生分级抑制作用,其半数抑制剂量(即使对照反应降低50%的剂量)分别约为30、19和> 30 mg kg-1。在吲哚-3-丁酸和吲哚-3-乙酸培养基中获得的叶下珠愈伤组织提取物(3 - 90 mg kg-1,腹腔注射)产生类似的镇痛作用。在福尔马林试验中,在吲哚丁酸培养基中获得的叶下珠提取物(3 - 100 mg kg-1,腹腔注射)仅抑制福尔马林诱导疼痛的第二阶段,半数抑制剂量约为100 mg kg-1。叶下珠和科科瓦多叶下珠的吲哚乙酸和吲哚丁酸甲醇提取物(10 - 100 mg kg-1,腹腔注射)剂量依赖性地抑制福尔马林诱导疼痛的两个阶段(第二阶段的半数抑制剂量分别约为100和52 mg kg-1)。然而,叶下珠愈伤组织提取物未能影响福尔马林诱导的爪肿胀以及甩尾试验中对辐射热的反应。此外,纳洛酮可完全拮抗吗啡的镇痛作用,但不能拮抗叶下珠愈伤组织提取物引起的镇痛作用。(摘要截短至250字)

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