Imafidon Christian Eseigbe, Akomolafe Rufus Ojo, Sanusi Abubakar Abefe, Ogundipe Oluwadare Joshua, Olukiran Olaoluwa Sesan, Ayowole Oladele Abraham
Department of Physiological Sciences, Faculty of Basic Medical Sciences, Obafemi Awolowo University, Ile-Ife, Osun, Nigeria.
Department of Medicine, Obafemi Awolowo University, Ile-Ife, Osun, Nigeria.
J Intercult Ethnopharmacol. 2015 Oct-Dec;4(4):284-92. doi: 10.5455/jice.20151107021034. Epub 2015 Nov 13.
To determine the effects of polyphenol-rich extract of the leaves of Vernonia amygdalina (PEVA) on the feeding pattern of rats that were exposed to cadmium (Cd) toxicity.
Thirty male Wistar rats, weighing 160-180 g, were divided into 6 groups of 5 rats each as follows; Group 1 received distilled water orally (0.2 ml/100 g), daily, throughout the period of study. Group 2 received Cd alone (in the form of CdSO4) at 5 mg/kg/day via intraperitoneal route for 5 consecutive days. Group 3 were pre-treated with Cd as Group 2 and thereafter left untreated for a period of 4-week. After the oral lethal dose of PEVA was determined, Groups 4, 5, and 6 were pre-treated with Cd as Group 2 after which they received graded doses of PEVA at 100, 200 and 400 mg/kg/day (0.2 ml/100 g), respectively via oral route for 4 weeks. Blood samples were collected for some plasma biochemical assays while urine samples were collected using metabolic cages.
PEVA administration significantly increased (P < 0.05) the body weight and feeding patterns that were significantly reduced (P < 0.05) by Cd toxicity. PEVA also significantly reinstated the plasma antioxidant status, as well as glucose and urine volume of the rats toward control values (P < 0.05).
PEVA can be an herbal alternative in the treatment or management of subjects manifesting alterations in feeding pattern and urine volume that is Cd-induced.
确定扁桃斑鸠菊叶富含多酚的提取物(PEVA)对暴露于镉(Cd)毒性的大鼠进食模式的影响。
30只体重160 - 180克的雄性Wistar大鼠,分为6组,每组5只,分组如下:第1组在整个研究期间每天经口给予蒸馏水(0.2毫升/100克)。第2组通过腹腔注射途径连续5天给予单独的Cd(以CdSO4形式),剂量为5毫克/千克/天。第3组如第2组一样预先用Cd处理,然后4周不进行处理。在确定PEVA的口服致死剂量后,第4、5和6组如第2组一样预先用Cd处理,之后分别以100、200和400毫克/千克/天(0.2毫升/100克)的剂量经口给予分级剂量的PEVA,持续4周。采集血样进行一些血浆生化检测,同时使用代谢笼收集尿样。
给予PEVA显著增加了体重和进食模式(P < 0.05),而Cd毒性显著降低了体重和进食模式(P < 0.05)。PEVA还显著恢复了大鼠的血浆抗氧化状态以及血糖和尿量至对照值(P < 0.05)。
PEVA可作为一种草药替代品,用于治疗或管理表现出由Cd诱导的进食模式和尿量改变的受试者。