期刊论文详细信息
Chemistry Central Journal
Hexane soluble extract of Mallotus philippensis (Lam.) Muell. Arg. root possesses anti-leukaemic activity
Musa Khan2  Rizwana Aleem Qureshi4  Masroor Hussain3  Khalid Mehmood5  Rahmat Ali Khan1 
[1] Department of Biotechnology, Faculty of Biological Sciences, University of Science and Technology Bannu, Khyber Pakutunkhwa, Pakistan
[2] National Engineering and Scientific Commission (NESCOM), Rawalpindi, Pakistan
[3] Khyber Medical University, Peshawar, Pakistan
[4] Department of Plant Sciences, Quaid-i-Azam University Islamabad, Islamabad, Pakistan
[5] Department of Pharmacy, Hazara University Havelian Campus, Abbottabad, Pakistan
关键词: Cyclin D1;    Cdc25A;    GC-MS;    HL-60 cells;    Mallotus philippensis;   
Others  :  787837
DOI  :  10.1186/1752-153X-7-157
 received in 2013-03-13, accepted in 2013-09-10,  发布年份 2013
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【 摘 要 】

Background

Mallotus philippensis (Lam.) Muell. Arg. is a well known medicinal plant of Asia and Australia. Various compounds from different aerial parts of the plant have been reported possessing potent pharmacological, antiviral, antibacterial and cytotoxic activities. We were interested to determine the effects of some root extracts from M. philippensis on human promyelocytic leukemia HL-60 cell proliferation, cell cycle regulators and apoptosis in order to investigate its anti-leukemic potential.

Results

Root extract of M. philippensis was initially extracted in organic solvents, hexane, ethyl acetate, and n-butanol. The hexane extract showed highest toxicity against p53-deficient HL-60 cells (IC50 1.5 mg dry roots equivalent/ml medium) after 72 h and interestingly, inhibition of cell proliferation was preceded by the upregulation of the proto-oncogenes Cdc25A and cyclin D1 within 24 h. The hexane extract induced 18% apoptosis after 48 h of treatment. Chemical composition of the hexane extract was analyzed by GC-MS and the 90% fragments were matched with polyphenolic compounds.

Conclusions

The present study confirms that the hexane fraction of M. philippensis root extract possesses anti-leukemic activity in HL-60 cells. The polyphenols were the main compounds of the hexane extract that inhibited proliferation and induced apoptosis.

【 授权许可】

   
2013 Khan et al.; licensee Chemistry Central Ltd.

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【 参考文献 】
  • [1]Satyavati GV, Gupta KA, Tandon N: Medicinal Plants of India Volume 2. New Delhi: Indian Council of Medical Research; 1987:201-206.
  • [2]Gupta AK, Chauhan JS: Constituents from the stem of Bauhinia variegate. Nat Acad Sci Lett 1984, 7:15-16.
  • [3]Lounasmaa M, Widen CJ, Tuuf CM, Huhtikangas A: On the phloroglucinol derivatives of Mallotus philippinensis. Planta Med 1975, 28:16-31.
  • [4]Usmanghani K, Saeed A, Alam MT: Indusynic Medicine. Karachi: Research Institute of Indusyunic Medicine; 1997:285-287.
  • [5]Zabihullah O, Rasheed A, Akhter N: Ethnobotanical survey in Kot Manzaray Baba valley Pakistan. J Plant Sci 2006, 12:115-121.
  • [6]Arisawa M, Fujita A, Hayashi T, Morita N, Kikuchi T, Tezuka Y: Studies on cytotoxic constituents in pericarps of Mallotus japonicus. Chem Pharm Bull 1990, 38:698-700.
  • [7]Arisawa M, Fujita A, Morita N, Koshimura S: Cytotoxic and antitumor constituents in pericarps of Mallotus japonicas. Planta Med 1990, 56:377-379.
  • [8]Fujita A, Hayashi T, Arisawa M, Shimizu M, Morita N, Kikuchi T, Tezuka Y: Studies on cytotoxic constituents in pericarps of Mallotus japonicas. J Nat Prod 1988, 51:708-712.
  • [9]Daikonya A, Katsuki S, Wu JB, Kitanaka S: Anti-allergic agents from natural sources Anti-allergic activity of new phloroglucinol derivatives from Mallotus philippensis (Euphorbiaceae). Chem Pharm Bull 2002, 50:1566-1569.
  • [10]Zaidi SFH, Yoshida I, Butt F, Yusuf MA, Usmanghani K, Kadowaki M, Sugiyama T: Potent bactericidal constituents from Mallotus philippensis against Clarithromycin and Metronidazole resistant strains of Japanese and Pakistani Helicobacter pylori. Bio Pharma Bull 2009, 32:631-636.
  • [11]Nakane H, Arisawa M, Fujita A, Koshimura S, Ono K: Inhibition of HIV-reverse transcriptase activity by some phloroglucinol derivatives. FEBS Lett 1991, 286:83-85.
  • [12]Jabbar A, Raza MA, Iqbal Z, Khan MN: An inventory of the ethnobotanicals used as anthelmintics in the Southern Punjab (Pakistan). J Ethnopharm 2006, 108:152-154.
  • [13]Kumar VP, Chauhan NS, Padh H, Rajani M: Non-timber forest products of Nepal. J Ethnopharm 2006, 107:182-188.
  • [14]Tanaka R, Nakata T, Yamaguchi C, Wada S, Yamada T, Tokuda H: Potential anti-tumor-promoting activity of 3α-Hydroxy-D:A-friedooleanan-2-one from the stem bark of Mallotus philippensis. Planta Med 2008, 74:413-416.
  • [15]Grusch M, Polgar D, Gfatter S, Leuhuber K, Huettenbrenner S, Leisser C: Maintenance of ATP favours apoptosis over necrosis triggered by benzamide riboside. Cell Death Diff 2002, 9:169-178.
  • [16]Bandopandhyay M, Dhingra VK, Mukerjee SK, Pardeshi NP, Seshadri TR: Triterpenoids and other components of Mallotus philippensis. Euphorbiaceae. Phytochem 1972, 11:1511.
  • [17]Ahluwalia VK, Sharma ND, Mittal B, Gupata SR: Novel prenylated flavanoids from Mallotus philippensis. Muell Arg Ind J Chem 1988, 27B:238-241.
  • [18]Tanaka T, Ito T, Iinuma M, Takahashit Y, Naganaw H: Dimeric chalcone derivatives from Mallotus philippensis. Phytochem 1998, 48:1423-1427.
  • [19]Furusawa M, Ido Y, Tanaka T, Ito T, Nakaya K, Ibrahim I: Novel, complex flavonoids from Mallotus philippensis (Kamala tree). H Chim Act 2005, 88:1048-1058.
  • [20]Kikuchi T, Toyoda T: Isolation and structure determination of pachysandiol-A and a note on the stereochemistry of cerin. Tetrhedran Lett 1967, 33:3181-3185.
  • [21]Talapatra SK, Pradhan DK, Talapatra B: Terpenoids and related compounds: part XV. 3á-Hydroxyfriedel-2-one and 2â-acetoxyfriedel-3-one (epicerin acetate), two new pentacyclic triterpenoids from cork waste, their partial syntheses and one-step conversions to friedelin. Ind J Chem 1978, 16:361-365.
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