Acute and subacute toxicity study of 1,8-cineole in mice

被引:0
|
作者
Xu, Jiao [1 ,4 ]
Hu, Zhi-Qiang [1 ]
Wang, Chuan [1 ]
Yin, Zhong-Qiong [1 ]
Wei, Qin [2 ]
Zhou, Li-Jun [1 ]
Li, Li [1 ]
Du, Yong-Hua [2 ]
Jia, Ren-Yong [1 ]
Li, Mei [3 ]
Fan, Qiao-Jia [1 ]
Liang, Xiao-Xia [1 ]
He, Chang-Liang [1 ]
Yin, Li-Zi [1 ]
机构
[1] Sichuan Agr Univ, Coll Vet Med, Yaan 625014, Sichuan, Peoples R China
[2] Yibin Coll, Key Lab Southwest Special Econ Plant Protect & Ut, Yibin 644000, Peoples R China
[3] Sichuan Agricutural Univ, Coll Forestry, Yaan 625014, Peoples R China
[4] Leshan Vocat & Tech Coll, Leshan 614000, Peoples R China
基金
中国国家自然科学基金;
关键词
1,8-cineole; toxicity; histopathology; ultrastructural changes; mice; ESSENTIAL OIL; EUCALYPTUS; RATS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of acute and subacute toxicity of 1,8-cineole in Kunming mice were studied. After acute oral administration, the LD50 value (95% CL) was 3849 mg/kg (3488.8 similar to 4247.1 mg/kg). In the subacute toxicity study, there were no significant differences in body weight and relative organ weight between the control group and 1,8-cineole treatment groups. The histopathological examinations showed that granular degeneration and vacuolar degeneration appeared in liver and kidney tissue after administration of high dose of 1,8-cineole. Under electron microscopy, a series of ultrastructural changes were observed: The electron microscopy assays indicated that the influence of 1,8-cineole on the target organ at the subcellular level were mainly on the mitochondria, endoplasmic reticulum and other membrane type structure of liver and kidney.
引用
收藏
页码:1495 / 1501
页数:7
相关论文
共 50 条
  • [21] 1,8-CINEOLE FROM ALPHA-TERPINEOL
    COXON, JM
    HARTSHOR.MP
    MITCHELL, JW
    RICHARDS, KE
    CHEMISTRY & INDUSTRY, 1968, (20) : 652 - &
  • [22] Enhanced chlorhexidine skin penetration with 1,8-cineole
    A. L. Casey
    T. J. Karpanen
    B. R. Conway
    T. Worthington
    P. Nightingale
    R. Waters
    T. S. J. Elliott
    BMC Infectious Diseases, 17
  • [23] Evolution and Occurrence of 1,8-Cineole (Eucalyptol) in Australian Wine
    Capone, Dimitra L.
    Van Leeuwen, Katryna
    Taylor, Dennis K.
    Jeffery, David W.
    Pardon, Kevin H.
    Elsey, Gordon M.
    Sefton, Mark A.
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2011, 59 (03) : 953 - 959
  • [24] Biological Activity of 1,8-Cineole from Levant Wormwood
    Zh. K. Asanova
    E. M. Suleimenov
    G. A. Atazhanova
    A. D. Dembitskii
    R. N. Pak
    A. Dar
    S. M. Adekenov
    Pharmaceutical Chemistry Journal, 2003, 37 (1) : 28 - 30
  • [25] STEREOSPECIFIC HYDROXYLATION OF 1,8-CINEOLE USING A MICROBIAL BIOCATALYST
    LIU, WG
    ROSAZZA, JPN
    TETRAHEDRON LETTERS, 1990, 31 (20) : 2833 - 2836
  • [26] 1,8-Cineole: a review of source, biological activities, and application
    Cai, Zi-Min
    Peng, Jian-Qing
    Chen, Yi
    Tao, Ling
    Zhang, Yan-Yan
    Fu, Ling-Yun
    Long, Qing-De
    Shen, Xiang-Chun
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2021, 23 (10) : 938 - 954
  • [27] Eucalyptol (1,8-cineole): an underutilized ally in respiratory disorders?
    Galan, Derick M.
    Ezeudu, Ngozi E.
    Garcia, Jasmine
    Geronimo, Chalice A.
    Berry, Nicholas M.
    Malcolm, Benjamin J.
    JOURNAL OF ESSENTIAL OIL RESEARCH, 2020, 32 (02) : 103 - 110
  • [28] STEREOCHEMISTRY OF 1,8-CINEOLE DERIVATIVES - 2-CINEOLYLAMINES
    BONDAVALLI, F
    MINARDI, G
    SCHENONE, P
    ANNALI DI CHIMICA, 1970, 60 (12) : 829 - +
  • [29] 1,8-Cineole: Chemical and Biological Oxidation Reactions and Products
    Azerad, Robert
    CHEMPLUSCHEM, 2014, 79 (05): : 634 - 655
  • [30] 1,8-cineole: An attractant for the banana weevil, Cosmopolites sordidus
    Ndiege, IO
    Budenberg, WJ
    Otieno, DO
    Hassanali, A
    PHYTOCHEMISTRY, 1996, 42 (02) : 369 - 371