Ray S, Bagchi D, Lim P M, Bagchi M, Gross S M, Kothari S C, Preuss H G, Stohs S J
Department of Pharmacology, Toxicology and Medicinal Chemistry, Arnold & Marie Schwartz College of Pharmacy and Health Sciences Long Island University, Brooklyn, NY 11201, USA.
Res Commun Mol Pathol Pharmacol. 2001 Mar-Apr;109(3-4):165-97.
Grape seed proanthocyanidins are known to possess a broad spectrum of pharmacological, medicinal and therapeutic properties. Previous studies in our laboratories have demonstrated the various protective abilities of a novel IH636 grape seed proanthocyanidin extract (GSPE) against various pathologic conditions. However no extensive safety studies have been conducted on grape seed proanthocyanidins to date. This study demonstrates the acute and chronic safety studies on GSPE. Acute oral toxicity, dermal toxicity, dermal irritation and eye irritation studies have been conducted. The LD50 of GSPE was found to be greater than 5000 mg/kg when administered once orally via gastric intubation to fasted male and female albino rats. The LD50 of GSPE was found to be greater than 2000 mg/kg when administered once for 24 hr to the clipped, intact skin of male and female albino rats. In addition, 2000 mg/kg was found to be the no-observed-effect level (NOEL) for systemic toxicity under the conditions of the study. In a dermal irritation study, GSPE received a descriptive rating classification of moderately irritating. Extensive chronic studies were also conducted. We have assessed the effects of chronic administration of 100 mg GSPE/kg/day for twelve months and its effect on seven vital target organs, namely, brain, heart, intestine, kidney, liver, lung and spleen, and on serum chemistry changes in male B6C3F1 mice. Furthermore, the dose-dependent chronic effects of GSPE in female B6C3F1 mice were evaluated. Mice were fed 0, 100, 250 or 500 mg GSPE/kg/day for six months and the effects of GSPE exposure were examined on brain, duodenum, heart, kidney, liver, lung, pancreas and spleen, and on serum chemistry changes in female mice. These acute studies demonstrated that GSPE is safe and did not cause any detrimental effects in vivo under the conditions investigated in this study.
已知葡萄籽原花青素具有广泛的药理、药用和治疗特性。我们实验室之前的研究已经证明了一种新型的IH636葡萄籽原花青素提取物(GSPE)对各种病理状况的多种保护能力。然而,迄今为止尚未对葡萄籽原花青素进行广泛的安全性研究。本研究展示了对GSPE的急性和慢性安全性研究。已经进行了急性经口毒性、皮肤毒性、皮肤刺激性和眼刺激性研究。当通过胃管对禁食的雄性和雌性白化大鼠一次性经口给药时,发现GSPE的半数致死量(LD50)大于5000毫克/千克。当对雄性和雌性白化大鼠的剪毛完整皮肤一次性给药24小时时,发现GSPE的LD50大于2000毫克/千克。此外,在本研究条件下,发现2000毫克/千克是全身毒性的未观察到有害作用水平(NOEL)。在一项皮肤刺激性研究中,GSPE获得了中度刺激性的描述性评级分类。还进行了广泛的慢性研究。我们评估了连续十二个月每天以100毫克GSPE/千克的剂量慢性给药对雄性B6C3F1小鼠的七个重要靶器官,即脑、心脏、肠道、肾脏、肝脏、肺和脾脏的影响,以及对血清化学变化的影响。此外,还评估了GSPE在雌性B6C3F1小鼠中的剂量依赖性慢性影响。给小鼠喂食0、100、250或500毫克GSPE/千克/天,持续六个月,并检查GSPE暴露对雌性小鼠的脑、十二指肠、心脏、肾脏、肝脏、肺、胰腺和脾脏的影响,以及对血清化学变化的影响。这些急性研究表明,在本研究调查的条件下,GSPE是安全的,在体内不会引起任何有害影响。