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葡萄叶水醇提取物对奥沙利铂神经毒性的作用:体外和体内证据。

Effect of Vitis vinifera hydroalcoholic extract against oxaliplatin neurotoxicity: in vitro and in vivo evidence.

机构信息

Department of Neuroscience, Psychology, Drug Research and Child Health - NEUROFARBA - Pharmacology and Toxicology Section, University of Florence, Florence, Viale Gaetano Pieraccini 6, 50139, Italy.

Aboca S.p.A. Società Agricola, Località Aboca, Sansepolcro, Arezzo, 52100, Italy.

出版信息

Sci Rep. 2018 Sep 25;8(1):14364. doi: 10.1038/s41598-018-32691-w.

DOI:10.1038/s41598-018-32691-w
PMID:30254294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6156221/
Abstract

Oxaliplatin treatment is associated with the development of a dose-limiting painful neuropathy impairing patient's quality of life. Since oxidative unbalance is a relevant mechanism of oxaliplatin neurotoxicity, we assessed the potential antioxidant properties of Vitis vinifera extract in reducing oxaliplatin-induced neuropathy as a valuable therapeutic opportunity. A hydroalcoholic extract of Vitis vinifera red leaf was characterized and tested in primary rat astrocyte cells treated with oxaliplatin (100 μM). Oxaliplatin lethality in the human adenocarcinoma cell line HT-29 was evaluated in the absence and presence of the extract. In vivo, pain hypersensitivity was measured in a rat model of neuropathy induced by oxaliplatin and ex vivo molecular targets of redox balance were studied. Vitis vinifera extract (50 μg mL, 4 h incubation) significantly reduced the oxaliplatin-dependent superoxide anion increase and lipid peroxidation in rat astrocytes but did not interfere with the mortality elicited by oxaliplatin in HT-29 cancer cells. In oxaliplatin-treated rats, a repeated daily administration of the Vitis vinifera extract (300 mg kg, p.o.) significantly prevented mechanical and thermal hypersensitivity to noxious and non noxious stimuli. mRNA and protein levels of Nrf2 were normalized in spinal cord and DRGs. Moreover, in the spinal cord, the extract significantly decreased the activation of astrocytes. Vitis vinifera reduced oxidative damages and relieved pain without influencing oxaliplatin anti-cancer activity.

摘要

奥沙利铂治疗与发展剂量限制的痛性周围神经病有关,损害患者的生活质量。由于氧化失衡是奥沙利铂神经毒性的一个相关机制,我们评估了葡萄(Vitis vinifera)叶提取物的潜在抗氧化特性,以减少奥沙利铂诱导的周围神经病,作为一种有价值的治疗机会。对葡萄(Vitis vinifera)红叶片的水醇提取物进行了表征,并在奥沙利铂(100 μM)处理的原代大鼠星形胶质细胞中进行了测试。在不存在和存在提取物的情况下,评估了奥沙利铂对人结肠癌细胞系 HT-29 的致死作用。在奥沙利铂诱导的周围神经病大鼠模型中测量了体内疼痛敏感性,并研究了氧化还原平衡的分子靶标。葡萄(Vitis vinifera)提取物(50 μg mL,4 小时孵育)显著降低了奥沙利铂依赖的大鼠星形胶质细胞中超氧阴离子增加和脂质过氧化,但不影响奥沙利铂在 HT-29 癌细胞中引起的死亡率。在奥沙利铂处理的大鼠中,重复每日给予葡萄(Vitis vinifera)提取物(300 mg kg,口服)可显著预防机械和热痛觉过敏对有害和非有害刺激。脊髓和 DRG 中的 Nrf2 的 mRNA 和蛋白水平均正常化。此外,在脊髓中,提取物显著降低了星形胶质细胞的激活。葡萄(Vitis vinifera)减轻了氧化损伤并缓解了疼痛,而不影响奥沙利铂的抗癌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/91b655c41166/41598_2018_32691_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/777ddae0b9bf/41598_2018_32691_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/19a4f58d311a/41598_2018_32691_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/2036f6e85c52/41598_2018_32691_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/d3e68094e7bf/41598_2018_32691_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/07ed5627597c/41598_2018_32691_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/40b54ae4f0dc/41598_2018_32691_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/ddb3af32abd0/41598_2018_32691_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/004e55bd92ce/41598_2018_32691_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/91b655c41166/41598_2018_32691_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/777ddae0b9bf/41598_2018_32691_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/19a4f58d311a/41598_2018_32691_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/2036f6e85c52/41598_2018_32691_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/d3e68094e7bf/41598_2018_32691_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/07ed5627597c/41598_2018_32691_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/40b54ae4f0dc/41598_2018_32691_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/ddb3af32abd0/41598_2018_32691_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/004e55bd92ce/41598_2018_32691_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6072/6156221/91b655c41166/41598_2018_32691_Fig9_HTML.jpg

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