Influence of α-tocopherol, propolis and piperine on therapeutic potential of tiferron against beryllium induced toxic manifestations

被引:24
作者
Nirala, Satendra Kumar [1 ,3 ]
Bhadauria, Monika [1 ,4 ]
Mathur, Ramesh [1 ]
Mathur, Asha [2 ]
机构
[1] Jiwaji Univ, Sch Studies Zool, Gwalior 474011, India
[2] KRG Coll, Gwalior 474009, India
[3] Lanzhou Univ, Inst Cell Biol, Sch Life Sci, Lanzhou 730000, Peoples R China
[4] Lanzhou Univ, Natl Lab Appl Org Chem, Lanzhou 730000, Peoples R China
关键词
beryllium toxicity; biochemical alterations; tiferron; alpha-tocopherol; propolis; piperine; combined therapy;
D O I
10.1002/jat.1250
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The therapeutic potential of the chelator tiferron (sodium-4,5-dihydroxy-1,3-benzene disulphonate; 300 mg kg(-1), i.p.) and adjuvants, i.e. alpha-tocopherol (25 mg kg(-1), p.o.), propolis (a honey-bee hive product; 200 mg kg(-1), p.o.) and piperine (10 mg kg(-1), p.o.) were evaluated individually and in combination against beryllium induced biochemical alterations and oxidative stress consequences. Female albino rats were exposed to beryllium nitrate (1 mg kg(-1), i.p.) daily for 28 days followed by treatment with the above mentioned therapeutic agents for 5 consecutive days. Administration of beryllium altered blood biochemical variables with significant depletion in hemoglobin, blood sugar, total serum protein, albumin and significant enhancement in the release of serum transaminases. A significantly increased lipid peroxidation and a decreased level of glutathione after beryllium exposure indicated oxidative stress in the liver and kidney. Beryllium exposure decreased total protein and glycogen contents, whereas triglycerides and cholesterol increased significantly in liver and kidney. Individual administration of all the four compounds showed significant therapeutic potential in reverse of some of the biochemical parameters mentioned above. Furthermore, the combination of tiferron with a-tocopherol, propolis or piperine, respectively, could reverse all the variables significantly more towards the control. None of the test compounds showed any significant change in choleretic activity (bile flow and bile solids), indicating that these compounds had no adverse effects at these dose levels. It was concluded that all the combinations of tiferron and adjuvants played a beneficial role in reducing beryllium induced systemic toxicity at relatively lower doses and the combination of tiferron and propolis showed a more pronounced therapeutic potential. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:44 / 54
页数:11
相关论文
共 81 条
  • [1] INHIBITION OF PHOSPHOGLUCOMUTASE BY BERYLLIUM
    ALDRIDGE, WN
    THOMAS, M
    [J]. BIOCHEMICAL JOURNAL, 1966, 98 (01) : 100 - +
  • [2] [Anonymous], 2002, Agency for toxic substances and disease registry
  • [3] ARKHIPOVA OG, 1964, DOKL AKAD NAUK SSSR+, V158, P1235
  • [4] ASATOOR AM, 1954, PROCESS BIOCH 0116, P56
  • [5] Piperine derived from black pepper increases the plasma levels of coenzyme Q10 following oral supplementation
    Badmaev, V
    Majeed, M
    Prakash, L
    [J]. JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2000, 11 (02) : 109 - 113
  • [6] EFFECT OF PIPERINE ON BIOAVAILABILITY AND PHARMACOKINETICS OF PROPRANOLOL AND THEOPHYLLINE IN HEALTHY-VOLUNTEERS
    BANO, G
    RAINA, RK
    ZUTSHI, U
    BEDI, KL
    JOHRI, RK
    SHARMA, SC
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1991, 41 (06) : 615 - 617
  • [7] Recent progress in pharmacological research of propolis
    Banskota, AH
    Tezuka, Y
    Kadota, S
    [J]. PHYTOTHERAPY RESEARCH, 2001, 15 (07) : 561 - 571
  • [8] Chemical constituents of Brazilian propolis and their cytotoxic activities
    Banskota, AH
    Tezuka, Y
    Prasain, JK
    Matsushige, K
    Saiki, I
    Kadota, S
    [J]. JOURNAL OF NATURAL PRODUCTS, 1998, 61 (07): : 896 - 900
  • [9] BEUTLER E, 1988, MODERN NUTR HLTH DIS, P298
  • [10] EFFECTIVENESS OF SODIUM 4,5-DIHYDROXYBENZENE-1,3-DISULFONATE (TIRON) IN PROTECTING AGAINST URANIUM-INDUCED DEVELOPMENTAL TOXICITY IN MICE
    BOSQUE, MA
    DOMINGO, JL
    LLOBET, JM
    CORBELLA, J
    [J]. TOXICOLOGY, 1993, 79 (02) : 149 - 156