Shoaib Mohammad, Shah Syed Wadood Ali, Ali Niaz, Shah Ismail, Ullah Shafi, Ghias Mehreen, Tahir Muhammad Nawaz, Gul Farah, Akhtar Sohail, Ullah Abd, Akbar Wajid, Ullah Asad
Department of Pharmacy, University of Malakand, Malakand, Khyber Pakhtunkhwa, Pakistan.
Department of Pharmacology, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Khyber Pakhtunkhwa, Pakistan.
BMC Complement Altern Med. 2016 Jun 13;16:178. doi: 10.1186/s12906-016-1157-2.
Tissue damage is associated with pain, which is an alarming sign. Aspirin and morphine have been widely used in recent decades for management of pain. Medicinal herbs have been in use for treatment of different diseases for centuries. Many of these herbs possess analgesic activity with relatively less incidences of adverse effects. The strong positive correlation of alkaloids in medicinal plants for analgesic activity persuades an intention to determine possible analgesic activity of total alkaloids extracted from the selected medicinal plants using animal models to answer its possible mechanisms.
Crude alkaloids from selected medicinal plants (Woodfordia fruticosa, Adhatoda vasica, Chenopodium ambrosioides, Vitex negundo, Peganum harmala and Broussonetia papyrifera) were extracted as per reported literature. The test crude alkaloids were screened foracute toxicity study. Writhings induced by acetic acid, tail immersion method and formalin-induced nociception assay procedures were used for possible analgesic effects of the crude alkaloids.
Crude alkaloids were safe up to dose of 1250 mg/kg body weight in mice. The alkaloids significantly reduced the abdominal constrictions, and increased the time for paw licking response in both phases with a significant raise in latency time in nociception models (P ≤ 0.05). Moreover, the antinociceptive response was significantly attenuated by pretreatment with naloxone suggesting involvement of the opioid receptors for possible antinociceptive action.
Crude alkaloids of Woodfordia fruticosa and Peganum harmala showed prominent analgesic potentials through inhibition of peripheral as well as central nervous system mechanisms. Further work is required for isolation of the pharmacologically active constituents.
组织损伤与疼痛相关,疼痛是一种警示信号。近几十年来,阿司匹林和吗啡已被广泛用于疼痛管理。几个世纪以来,草药一直用于治疗各种疾病。这些草药中的许多都具有镇痛活性,且不良反应发生率相对较低。药用植物中生物碱与镇痛活性的强正相关促使人们有意使用动物模型来确定从选定药用植物中提取的总生物碱的可能镇痛活性,并探究其可能的作用机制。
按照已报道的文献方法,从选定的药用植物(紫铆、鸭嘴花、土荆芥、黄荆、骆驼蓬和构树)中提取粗生物碱。对受试粗生物碱进行急性毒性研究。采用乙酸诱导扭体法、热板法和福尔马林诱导的伤害感受试验程序来检测粗生物碱的可能镇痛作用。
在小鼠中,粗生物碱在高达1250mg/kg体重的剂量下是安全的。生物碱显著减少了腹部收缩次数,并增加了两个阶段舔爪反应的时间,同时伤害感受模型中的潜伏期显著延长(P≤0.05)。此外,用纳洛酮预处理后,抗伤害感受反应显著减弱,提示阿片受体可能参与了抗伤害感受作用。
紫铆和骆驼蓬的粗生物碱通过抑制外周及中枢神经系统机制显示出显著的镇痛潜力。需要进一步开展工作以分离出药理活性成分。