Ameliorative Potentials of Quercetin against Lead-Induced Hematological and Testicular Alterations in Albino Rats

被引:16
作者
Al-Omair, Mohammed A. [1 ]
Sedky, Azza [2 ]
Ali, Awatef [2 ]
Elsawy, Hany [1 ,3 ]
机构
[1] King Faisal Univ, Dept Chem, Coll Sci, Al Ahsaa, Saudi Arabia
[2] Univ Alexandria, Dept Zool, Fac Sci, Alexandria, Egypt
[3] Tanta Univ, Dept Chem, Fac Sci, Tanta, Egypt
来源
CHINESE JOURNAL OF PHYSIOLOGY | 2017年 / 60卷 / 01期
关键词
blood; lead acetate toxicity; quercetin; testicular alteration; INDUCED OXIDATIVE STRESS; HEAVY-METAL EXPOSURE; SPERM; ACETATE; DAMAGE;
D O I
10.4077/CJP.2017.BAF440
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Lead is one of the oldest environmental and occupational toxins. Health hazards from increased lead exposure as a result of industrial and environmental pollution are recognized. The aim of the present study was to investigate the protective effects of quercetin as a model of an antioxidant drug against the toxic effects of lead acetate on the blood and the testis of rats. The lead concentrations were determined in blood and the testis. Testosterone (T), luteinizing hormone (LH) and follicle stimulating hormone (FSH) were assessed in serum. Hemoglobin (Hb) content, packed cell volume (PCV), white blood cell (WBC) and red blood cell (RBC) counts were evaluated in the whole blood. Our results showed that administration of lead acetate was associated with an increased lead levels in blood as well as in the testis. Lead acetate administration also caused a decrease in testicular function, Hb content, PCV and RBC count in comparison to the respective mean values of the control. In addition, lead acetate increased WBC count and induced alterations in sperm count, sperm motility and sperm abnormality and histopathology. In the contrary, administration of lead acetate along with quercetin partially restored the studied parameters to normal values. In conclusion, the treatment with quercetin may provide a partial protection against the toxic effects induced by lead acetate in blood and the testis of rats.
引用
收藏
页码:54 / 61
页数:8
相关论文
共 47 条
  • [21] Quercetin and Cancer Chemoprevention
    Gibellini, Lara
    Pinti, Marcello
    Nasi, Milena
    Montagna, Jonas P.
    De Biasi, Sara
    Roat, Erika
    Bertoncelli, Linda
    Cooper, Edwin L.
    Cossarizza, Andrea
    [J]. EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2011, 2011 : 1 - 15
  • [22] Grant L.D., 2009, Environmental Toxicants: Human Exposures and Their Health Effects, V3rd
  • [23] Procyanidin content and variation in some commonly consumed foods
    Hammerstone, JF
    Lazarus, SA
    Schmitz, HH
    [J]. JOURNAL OF NUTRITION, 2000, 130 (08) : 2086S - 2092S
  • [24] Flavonoids as peroxynitrite scavengers: the role of the hydroxyl groups
    Heijnen, CGM
    Haenen, GRMM
    van Acker, FAA
    van der Vijgh, WJF
    Bast, A
    [J]. TOXICOLOGY IN VITRO, 2001, 15 (01) : 3 - 6
  • [25] Relationships between reproductive performance and organochlorine contaminants in great black-backed gulls (Larus marinus)
    Helberg, M
    Bustnes, JO
    Erikstad, KE
    Kristiansen, KO
    Skaare, JU
    [J]. ENVIRONMENTAL POLLUTION, 2005, 134 (03) : 475 - 483
  • [26] Detection of the effects of repeated dose combined propoxur and heavy metal exposure by measurement of certain toxicological, haematological and immune function parameters in rats
    Institóris, L
    Siroki, O
    Ündeger, Ü
    Basaran, N
    Banerjee, BD
    Dési, I
    [J]. TOXICOLOGY, 2001, 163 (2-3) : 185 - 193
  • [27] Ismail HAA., 2014, J APPL LIFE SCI INT, V1, P1, DOI [10.9734/JALSI/2014/12057, DOI 10.9734/JALSI/2014/12057]
  • [28] Contribution of protein kinase C and glutamate in Pb2+-induced cytotoxicity
    Jadhav, AL
    Ramesh, GT
    Gunasekar, PG
    [J]. TOXICOLOGY LETTERS, 2000, 115 (02) : 89 - 98
  • [29] Khairwal V., 2015, INT J ADV RES SCI EN, V4, P289
  • [30] Inhibitory effects of flavonoids on free radical-induced hemolysis and their oxidative effects on hemoglobin
    Kitagawa, S
    Sakamoto, H
    Tano, H
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (08) : 999 - 1001