Heba Abuzaied, Dina Bashir, Eman Rashad, Maha Rashad, Hany El-Habback
{"title":"人参提取物可减轻大鼠模型中二氧化钛纳米颗粒的肾毒性","authors":"Heba Abuzaied, Dina Bashir, Eman Rashad, Maha Rashad, Hany El-Habback","doi":"10.21608/javs.2024.253254.1296","DOIUrl":null,"url":null,"abstract":"Titanium dioxide nanoparticles (TiO 2 -NPs) are widely utilized in cosmetics, food, and paintings. Although TiO 2 -NPs may cause toxicity through a variety of routes, oxidative stress is by far the most common. Ginseng is employed in a variety of medical applications because of its potency as an antioxidant. Thus, the purpose of this study is to assess the protective and therapeutic benefits of Panax ginseng against TiO 2 -NPs administration in the kidneys of male rats. Thirty-five mature male albino rats were divided into five groups of seven rats each at random. The experimental groups were as follows: Group I served as the control group; Group II received 200 mg/kg of ginseng orally; Group III received 200 mg/kg of TiO 2 - NPs orally; Group IV served as the protective group; rats were pretreated with ginseng 1 hour before TiO 2 -NPs at a dose similar to GII and GIII, respectively; and Group V served as the treatment group; rats received TiO 2 -NPs for 14 days, then ginseng for another 14 days at a dose identical to GIII and GII, respectively . After 4 weeks, serum samples were collected, and kidney tissues were dissected for biochemical and histopathological examinations. Treatment with TiO 2 -NPs elevated malonaldehyde (MDA), kidney biomarkers, and reduced glutathione (GSH) and glutathione peroxidase (GPx) levels. Furthermore, TiO 2 -NPs induce upregulation of cysteine-aspartic acid protease (caspase3) and cyclooxygenase (COX-2). Histopathologically, TiO 2 -NPs caused degenerative changes in renal tissue, including renal corpuscles, and showed hypertrophy with capillary congestion. Most renal tubules showed marked luminal dilation with epithelial cell flattening. Additionally, there was reduced immunoreactivity of Ki-67 in the kidney sections. Ginseng, on the other hand, substantially mitigated the detrimental impacts that TiO 2 -NPs had on the rat renal tissues by down-regulating the genes for COX-2 and caspase3, restoring these biochemical and molecular parameters, and ameliorating the histological changes. In conclusion, ginseng could potentially be used to alleviate the renal toxicity brought on by TiO 2 -NPs.","PeriodicalId":15040,"journal":{"name":"Journal of Applied Veterinary Sciences","volume":"409 16","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ginseng Extract can alleviate The Induced-renal Toxicity of Titanium Dioxide Nanoparticles in a Rat Model\",\"authors\":\"Heba Abuzaied, Dina Bashir, Eman Rashad, Maha Rashad, Hany El-Habback\",\"doi\":\"10.21608/javs.2024.253254.1296\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Titanium dioxide nanoparticles (TiO 2 -NPs) are widely utilized in cosmetics, food, and paintings. Although TiO 2 -NPs may cause toxicity through a variety of routes, oxidative stress is by far the most common. Ginseng is employed in a variety of medical applications because of its potency as an antioxidant. Thus, the purpose of this study is to assess the protective and therapeutic benefits of Panax ginseng against TiO 2 -NPs administration in the kidneys of male rats. Thirty-five mature male albino rats were divided into five groups of seven rats each at random. The experimental groups were as follows: Group I served as the control group; Group II received 200 mg/kg of ginseng orally; Group III received 200 mg/kg of TiO 2 - NPs orally; Group IV served as the protective group; rats were pretreated with ginseng 1 hour before TiO 2 -NPs at a dose similar to GII and GIII, respectively; and Group V served as the treatment group; rats received TiO 2 -NPs for 14 days, then ginseng for another 14 days at a dose identical to GIII and GII, respectively . After 4 weeks, serum samples were collected, and kidney tissues were dissected for biochemical and histopathological examinations. Treatment with TiO 2 -NPs elevated malonaldehyde (MDA), kidney biomarkers, and reduced glutathione (GSH) and glutathione peroxidase (GPx) levels. Furthermore, TiO 2 -NPs induce upregulation of cysteine-aspartic acid protease (caspase3) and cyclooxygenase (COX-2). Histopathologically, TiO 2 -NPs caused degenerative changes in renal tissue, including renal corpuscles, and showed hypertrophy with capillary congestion. Most renal tubules showed marked luminal dilation with epithelial cell flattening. Additionally, there was reduced immunoreactivity of Ki-67 in the kidney sections. Ginseng, on the other hand, substantially mitigated the detrimental impacts that TiO 2 -NPs had on the rat renal tissues by down-regulating the genes for COX-2 and caspase3, restoring these biochemical and molecular parameters, and ameliorating the histological changes. 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引用次数: 0
摘要
二氧化钛纳米粒子(TiO 2 -NPs)被广泛应用于化妆品、食品和绘画中。尽管 TiO 2 -NPs 可通过多种途径产生毒性,但氧化应激是迄今为止最常见的一种。人参具有抗氧化作用,因此被广泛应用于各种医疗领域。因此,本研究的目的是评估人参对雄性大鼠肾脏施用 TiO 2 -NPs 的保护和治疗作用。35 只成熟的雄性白化大鼠被随机分为 5 组,每组 7 只。实验组如下I 组为对照组;II 组口服 200 毫克/千克人参;III 组口服 200 毫克/千克 TiO 2 - NPs;IV 组为保护组,大鼠在服用 TiO 2 -NPs 前 1 小时服用人参,剂量分别与 GII 和 GIII 相同;V 组为治疗组,大鼠服用 TiO 2 -NPs 14 天,然后再服用人参 14 天,剂量分别与 GIII 和 GII 相同。4 周后,收集血清样本,解剖肾组织进行生化和组织病理学检查。用 TiO 2 -NPs 治疗会提高丙二醛(MDA)、肾脏生物标志物、还原型谷胱甘肽(GSH)和谷胱甘肽过氧化物酶(GPx)的水平。此外,TiO 2 -NPs还诱导半胱氨酸-天冬氨酸蛋白酶(caspase3)和环氧化酶(COX-2)的上调。从组织病理学角度看,TiO 2 -NPs导致包括肾小球在内的肾组织发生退行性变化,并表现出肥大和毛细血管充血。大多数肾小管管腔明显扩张,上皮细胞扁平。此外,肾切片中 Ki-67 的免疫活性降低。另一方面,人参通过下调 COX-2 和 caspase3 的基因,恢复了这些生化和分子参数,并改善了组织学变化,从而大大减轻了 TiO 2 -NPs 对大鼠肾组织的不利影响。总之,人参可用于减轻 TiO 2 -NPs 对肾脏的毒性。
Ginseng Extract can alleviate The Induced-renal Toxicity of Titanium Dioxide Nanoparticles in a Rat Model
Titanium dioxide nanoparticles (TiO 2 -NPs) are widely utilized in cosmetics, food, and paintings. Although TiO 2 -NPs may cause toxicity through a variety of routes, oxidative stress is by far the most common. Ginseng is employed in a variety of medical applications because of its potency as an antioxidant. Thus, the purpose of this study is to assess the protective and therapeutic benefits of Panax ginseng against TiO 2 -NPs administration in the kidneys of male rats. Thirty-five mature male albino rats were divided into five groups of seven rats each at random. The experimental groups were as follows: Group I served as the control group; Group II received 200 mg/kg of ginseng orally; Group III received 200 mg/kg of TiO 2 - NPs orally; Group IV served as the protective group; rats were pretreated with ginseng 1 hour before TiO 2 -NPs at a dose similar to GII and GIII, respectively; and Group V served as the treatment group; rats received TiO 2 -NPs for 14 days, then ginseng for another 14 days at a dose identical to GIII and GII, respectively . After 4 weeks, serum samples were collected, and kidney tissues were dissected for biochemical and histopathological examinations. Treatment with TiO 2 -NPs elevated malonaldehyde (MDA), kidney biomarkers, and reduced glutathione (GSH) and glutathione peroxidase (GPx) levels. Furthermore, TiO 2 -NPs induce upregulation of cysteine-aspartic acid protease (caspase3) and cyclooxygenase (COX-2). Histopathologically, TiO 2 -NPs caused degenerative changes in renal tissue, including renal corpuscles, and showed hypertrophy with capillary congestion. Most renal tubules showed marked luminal dilation with epithelial cell flattening. Additionally, there was reduced immunoreactivity of Ki-67 in the kidney sections. Ginseng, on the other hand, substantially mitigated the detrimental impacts that TiO 2 -NPs had on the rat renal tissues by down-regulating the genes for COX-2 and caspase3, restoring these biochemical and molecular parameters, and ameliorating the histological changes. In conclusion, ginseng could potentially be used to alleviate the renal toxicity brought on by TiO 2 -NPs.