Acute and sub acute toxicity study of Clerodendrum inerme, Jasminum mesnyi Hance and Callistetnon citrinus

被引:12
作者
Bhushan, Bharat [1 ]
Sardana, Satish [1 ]
Bansal, Gulshan [2 ]
机构
[1] Hindu Coll Pharm, Dept Pharrnacognosy, Sonepat, Haryana, India
[2] Panjabi Univ, Dept Pharmaceut Sci & Drug Res, Patiala, Punjab, India
关键词
Acute toxicity; Subacute toxicity; Albino rats; Clerodendrum inerme; Jasminum mesnyi Hance; Callisteinon citrinus;
D O I
10.1016/S2221-6189(14)60069-X
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To study acute and sub acute toxicity study inerme (C. inerme, Jasminum mesnyi (J. mesnyi) Hance and Callistemon citrinus). Methods: The acute toxicity test was conducted in Swiss albino mice. The extracts of C. inerme, J. mesnyi Hance and C. citrinus was administered in single dose of 0.5, 1.0, 2.0, 3.0, 4.0 and 5.0 g/kg and observed for behavioral changes and modality, if any. In sub-acute toxicity study, Wistar rats of either sex were administered 1/5th of the maximum tolerated dose, p.o. for 4 weeks. Rats were observed weekly for any change in their body weight, food and water intake during 28 d of the treatment. At the end of 28 d, blood samples of the rats were collected for hematological and biochemical study. Results: In acute toxicity study, all four extracts of three plants were found to be well tolerated up to the dose of 2 000 mg/kg. These produced neither mortality nor any change in the behavior in mice. In sob-acute toxicity study, all four extracts of three plants at the LDS dose level did not produce any significant alteration in hematological and biochemical parameters in rats. Conclusions: The results demonstrated that there is a wide margin of safety for the therapeutic use of each of the four extracts of three plants. The findings also corroborated the traditional use of these extracts.
引用
收藏
页码:324 / 327
页数:4
相关论文
共 23 条
  • [1] Bhardwaj S, 2012, INT J PHARM BIO SCI, V1, P103
  • [2] Biswas N. R., 1998, Indian Journal of Pharmacology, V30, P239
  • [3] Bonge KP, 2012, EUR J EXP BIOL, V2, P1284
  • [4] Burger C, 2005, J PHARM PHARM SCI, V8, P370
  • [5] INERMINOSIDE-A1, INERMINOSIDE-C AND INERMINOSIDE-D, 3 IRIDOID GLYCOSIDES FROM CLERODENDRUM INERME
    CALIS, I
    HOSNY, M
    YURUKER, A
    [J]. PHYTOCHEMISTRY, 1994, 37 (04) : 1083 - 1085
  • [6] Chatterjee A., 1997, TREATISE INDIAN MED, P17
  • [7] Deshpade J., 2006, HDB MED HERBS, P117
  • [8] Devbhuti D, 2008, ACTA POL PHARM, V65, P501
  • [9] Acute and chronic toxicological studies of Ajuga iva in experimental animals
    El Hilaly, J
    Israili, ZH
    Lyoussi, B
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2004, 91 (01) : 43 - 50
  • [10] Ghosh MN, 2008, FUNDAMENTALS EXPT PH, P176