Vaziri Zohreh, Abbassian Hassan, Sheibani Vahid, Haghani Masoud, Nazeri Masoud, Aghaei Iraj, Shabani Mohammad
Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
Histomorphometry and Stereology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran; Department of Physiology, Shiraz University of Medical Sciences, Shiraz, Iran.
Neurosci Lett. 2015 Mar 17;590:84-90. doi: 10.1016/j.neulet.2015.01.078. Epub 2015 Jan 30.
Essential tremor (ET) is a progressive neurological disorder with motor and non-motor symptoms. It has conclusively been shown that modulation of glutamate receptors could ameliorate ET. Recent studies have suggested that Berberine (BBR) has an inhibitory effect on glutamate receptors. Therefore, BBR may have therapeutic effects on ET. In this study, male Wistar rats (n=10 in each group) weighing 40-60 g were divided into control, harmaline (30 mg/kg, i.p.) and berberine (10, 20 or 50mg/kg, i.p, 15 min before harmaline injection) groups. Open field, rotarod, wire grip and foot print tests were used to evaluate motor performance. The results indicated that the administration of BBR (10 and 20mg/kg) attenuated harmaline-induced tremor in rats, but the beneficial effects of BBR could not be identified at dose 50mg/kg. In addition, BBR ameliorated gait disturbance in doses of 10 and 20mg/kg. The high dose of BBR not only failed to recover step width but also showed an adverse effect on left and right step length. The results indicate that BBR only in dose of 20mg/kg recovers mobility duration. The current study found a dose-dependent manner for the therapeutic effects of BBR in ET. Our study provides the initial evidence for the effects of BBR on motor function. Since BBR exerts its effects mainly through regulation of neurotransmitter release or blocke of NMDA receptors, thus, it is predicted that BBR ameliorate harmaline effect through blockade of NMDA receptors or glutamate release. This is an important issue for future research to evaluate the possible mechanisms involved.
特发性震颤(ET)是一种具有运动和非运动症状的进行性神经疾病。已有确凿证据表明,调节谷氨酸受体可改善特发性震颤。最近的研究表明,黄连素(BBR)对谷氨酸受体具有抑制作用。因此,BBR可能对特发性震颤具有治疗作用。在本研究中,将体重40 - 60克的雄性Wistar大鼠(每组n = 10)分为对照组、harmaline组(30毫克/千克,腹腔注射)和黄连素组(10、20或50毫克/千克,腹腔注射,在harmaline注射前15分钟)。采用旷场试验、转棒试验、握力试验和足迹试验评估运动性能。结果表明,给予BBR(10和20毫克/千克)可减轻harmaline诱导的大鼠震颤,但在50毫克/千克剂量下未发现BBR的有益作用。此外,BBR在10和20毫克/千克剂量下改善了步态障碍。高剂量的BBR不仅未能恢复步幅,而且对左右步长显示出不利影响。结果表明,仅20毫克/千克剂量的BBR可恢复活动持续时间。本研究发现BBR对特发性震颤的治疗作用呈剂量依赖性。我们的研究为BBR对运动功能的影响提供了初步证据。由于BBR主要通过调节神经递质释放或阻断NMDA受体发挥作用,因此,预计BBR通过阻断NMDA受体或谷氨酸释放来改善harmaline的作用。这是未来研究评估可能涉及的机制的一个重要问题。