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评价 chvar. 精油的镇痛潜力和安全性。

Evaluation of the analgesic potential and safety of chvar. essential oil.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu Province, China.

School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu Province, China.

出版信息

Bioengineered. 2021 Dec;12(2):9860-9871. doi: 10.1080/21655979.2021.1996149.

DOI:10.1080/21655979.2021.1996149
PMID:34699310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8810075/
Abstract

chvar. essential oil (BEO, 18.2% v/v borneol) is a by-product of steam distillation to produce natural crystalline borneol (NCB, 98.4% v/v borneol). Given the known medicinal properties of borneol, the analgesic function and safety were studied. Horn's method and the Draize test revealed a gender difference in mice regarding acute oral LD, i.e., low-toxicity to female mice (2749 mg/kg), but practically nontoxic to male mice (5081 mg/kg). There was no acute and skin or eye irritation when BEO was applied directly, if the BEO concentration was less than 50%. The analgesic effect of BEO was evaluated by the glacial acetic acid-induced writhing pain model. Continuous topical application of BEO to the abdomen of mice for 6 d, significantly reduced observed writhing in mice ( < 0.001) with a strong dose-response relationship (r = -0.9006). Concomitantly, the levels of the serum pain-related mediators, prostaglandin E (PGE) and transient receptor potential melastatin-8 (TRPM8) were significantly reduced ( < 0.001), and the latter showed a strong dose-response relationship (r = -0.9427). Therefore, BEO had similar analgesic functions to borneol and was demonstrated to be safe for medicinal use.

摘要

苍术酮(BEO,18.2%v/v 龙脑)是水蒸气蒸馏生产天然结晶龙脑(NCB,98.4%v/v 龙脑)的副产品。鉴于龙脑的已知药用特性,研究了其镇痛功能和安全性。Horn 法和 Draize 试验揭示了雌雄小鼠在急性口服 LD 方面存在性别差异,即雌鼠的低毒性(2749mg/kg),而雄鼠实际上无毒(5081mg/kg)。如果 BEO 浓度低于 50%,直接应用 BEO 不会引起急性皮肤或眼睛刺激。通过醋酸致小鼠扭体疼痛模型评价 BEO 的镇痛作用。连续 6d 局部应用 BEO 于小鼠腹部,明显减少观察到的小鼠扭体次数(<0.001),呈强剂量-反应关系(r=-0.9006)。同时,血清疼痛相关介质前列腺素 E(PGE)和瞬时受体电位 melastatin-8(TRPM8)的水平显著降低(<0.001),后者呈强剂量-反应关系(r=-0.9427)。因此,BEO 具有与龙脑相似的镇痛作用,且被证明可安全用于药用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/24c7cdd3d458/KBIE_A_1996149_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/b3ec8636887c/KBIE_A_1996149_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/7c6d03a8f0b3/KBIE_A_1996149_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/fd5594c5d24a/KBIE_A_1996149_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/043baca72f00/KBIE_A_1996149_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/050ddd222ad0/KBIE_A_1996149_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/24c7cdd3d458/KBIE_A_1996149_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/b3ec8636887c/KBIE_A_1996149_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/7c6d03a8f0b3/KBIE_A_1996149_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/fd5594c5d24a/KBIE_A_1996149_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/043baca72f00/KBIE_A_1996149_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/050ddd222ad0/KBIE_A_1996149_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a29/8810075/24c7cdd3d458/KBIE_A_1996149_F0005_B.jpg

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