Abstract
The aim of this experiment is to explore the effects of aluminum chloride (AlCl3) on the ATPase enzymes and gonadotropin receptors in the testes. Eighty male Wistar rats were orally exposed to 0 mg/kg body weight (BW) (control group, CG), 64 mg/kg BW (low-dose group, LG), 128 mg/kg BW (mid-dose group, MG), or 256 mg/kg BW (high-dose group, HG) for 120 days. The microstructure and ultrastructure of testes; the activities of Na+-K+-ATPase, Mg2+-ATPase, and Ca2+-ATPase; and the mRNA and protein expressions of follicle-stimulating hormone receptor (FSHR) and luteinizing hormone receptors (LHR) in the testes were examined. The results showed that the testes histological structure were damaged; the activities of Na+-K+-ATPase, Mg2+-ATPase, and Ca2+-ATPase, the mRNA and protein expressions of FSHR and LHR in the testes were all decreased in the rats with AlCl3 exposure. It indicates that AlCl3 causes the dysfunction of testes in rats.
Similar content being viewed by others
References
Tahmasbpour E, Balasubramanian D, Agarwal A (2014) A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART). J Assist Reprod Genet 31(9):1115–1137
Agarwal A, Tvrda E, Sharma R (2014) Relationship amongst teratozoospermia, seminal oxidative stress and male infertility. Reprod Biol Endocrinol 12:45
Oberholster PJ, Myburgh JG, Ashton PJ, Coetzee JJ, Botha AM (2012) Bioaccumulation of aluminium and iron in the food chain of Lake Loskop, South Africa. Ecotoxicol Environ Saf 75(1):134–141
Rengel Z (2004) Aluminum cycling in the soil-plant-animal-human continuum. Biometals 17:669–689
Djouina M, Esquerre N, Desreumaux P, Vignal C, Body-Malapel M (2016) Toxicological consequences of experimental exposure to aluminum in human intestinal epithelial cells. Food Chem Toxicol 91:108–116
Ige SF, Akhigbe RE (2012) The role of Allium Cepa on aluminum-induced reproductive dysfunction in experimental male rat models. J Hum Reprod Sci 5(2):200–205
Zhang F, Sun X, Yu H, Yang X, Song M, Han Y et al (2017) Effects of aluminum trichloride on the cartilage stimulatory growth factors in rats. Biometals 30(1):143–150
Moselhy WA, Helmy NA, Abdel-Halim BR, Nabil TM, Abdel-Hamid MI (2012) Role of ginger against the reproductive toxicity of aluminium chloride in albino male rats. Reprod Domest Anim 47(2):335–343
Abdel-Moneim AM (2013) Effects of taurine against histomorphological and ultrastructural changes in the testes of mice exposed to aluminium chloride. Arh Hig Rada Toksikol 64(3):405–414
Yousef MI, El-Morsy AM, Hassan MS (2005) Aluminium-induced deterioration in reproductive performance and seminal plasma biochemistry of male rabbits: protective role of ascorbic acid. Toxicology 215(1–2):97–107
Sushma NJ, Rao KJ (2007) Total ATPases activity in different tissues of albino mice exposed to aluminium acetate. J Environ Biol 28(2 Suppl):483–484
Fu Y, Jia FB, Wang J, Song M, Liu SM, Li YF et al (2014) Effects of sub-chronic aluminum chloride exposure on rat ovaries. Life Sci 100(1):61–66
Rawi SM, Seif Al Nassr FM (2015) Zinc sulphate and vitamin E alleviate reproductive toxicity caused by aluminium sulphate in male albino rats. Toxicol Ind Health 31(3):221–234
Zhu YZ, Sun H, Fu Y, Wang J, Song M, Li M et al (2014) Effects of sub-chronic aluminum chloride on spermatogenesis and testicular enzymatic activity in male rats. Life Sci 102:36–40
Li X, Huang W, Gu J, Du X, Lei L, Yuan X et al (2015) SREBP-1c overactivates ROS-mediated hepatic NF-κB inflammatory pathway in dairy cows with fatty liver. Cell Signal 27(10):2099–2109
Sun X, Yuan X, Chen L, Wang T, Wang Z, Sun G et al (2017) Histamine induces bovine rumen epithelial cell inflammatory response via NF-κB pathway. Cell Physiol Biochem 42(3):1109–1119
Sun H, Hu C, Jia L, Zhu Y, Zhao H, Shao B et al (2011) Effects of aluminum exposure on serum sex hormones and androgen receptor expression in male rats. Biol Trace Elem Res 144(1–3):1050–1058
Kopácek J, Hejzlar J, Kana J, Norton SA, Porcal P, Turek J (2009) Trends in aluminium export from a mountainous area to surface waters, from deglaciation to the recent: effects of vegetation and soil development, atmospheric acidification, and nitrogen-saturation. J Inorg Biochem 103:1439–1448
Speit G, Merkions O (2002) Evaluation of mutagenic effects of formaldehyde in vitro: detection of cross-links and mutat in mouse lymphoma cells. Mutagenesis 17:183–187
Zaman K, Zaman W, Siddique H (1993) Hematological and enzymatic results of aluminum intoxication in rats. Comp Biochem Physiol C 105(1):73–76
Silva VS, Gonçalves PP (2003) The inhibitory effect of aluminium on the (Na+/K+)ATPase activity of rat brain cortex synaptosomes. J Inorg Biochem 97(1):143–150
Ohyashiki T, Karino T, Suzuki S, Matsui K (1996) Effect of aluminum ion on Fe(2+)-induced lipid peroxidation in phospholipid liposomes under acidic conditions. J Biochem 120(5):895–900
Suwalsky M, Norris B, Villena F, Cuevas F, Sotomayor P, Zatta P (2004) Aluminum fluoride affects the structure and functions of cell membranes. Food Chem Toxicol 42(6):925–933
Mundy WR, Kodavanti PR, Dulchinos VF, Tilson HA (1994) Aluminum alters calcium transport in plasma membrane and endoplasmic reticulum from rat brain. J Biochem Toxicol 9(1):17–23
Garrosa M, Llanes F, Gayoso MJ (2011) Histopathological changes in gerbil liver and kidney after aluminum subchronic intoxication. Histol Histopathol 26(7):883–892
Nichol BE, Oliveira LA, Glass A, Siddiqi MY (1993) The effects of aluminum on the influx of calcium, potassium, ammonium, nitrate, and phosphate in an aluminum-sensitive cultivar of barley (Hordeum Vulgare L.) Plant Physiol 101(4):1263–1266
Gandolfi L, Stella MP, Zambenedetti P, Zatta P (1998) Aluminum alters intracellular calcium homeostasis in vitro. Biochim Biophys Acta 1406(3):315–320
Chaitanya TV, Mallipeddi K, Bondili JS, Nayak P (2012) Effect of aluminum exposure on superoxide and peroxide handling capacities by liver, kidney, testis and temporal cortex in rat. Indian J Biochem Biophys 49(5):395–398
Mailloux RJ, Hamel R, Appanna VD (2006) Aluminum toxicity elicits a dysfunctional TCA cycle and succinate accumulation in hepatocytes. J Biochem Mol Toxicol 20(4):198–208
Kajikawa M, Fujimoto S, Tsuura Y, Mukai E, Takeda T, Hamamoto Y et al (2002) Ouabain suppresses glucose-induced mitochondrial ATP production and insulin release by generating reactive oxygen species in pancreatic islets. Diabetes 51(8):2522–2529
Guo CH, Hsu GS, Chuang CJ, Chen PC (2009) Aluminum accumulation induced testicular oxidative stress and altered selenium metabolism in mice. Environ Toxicol Pharmacol 27(2):176–181
Maghraoui S, Clichici S, Ayadi A, Login C, Moldovan R, Daicoviciu D (2014) Oxidative stress in blood and testicle of rat following intraperitoneal administration of aluminum and indium. Acta Physiol Hung 101(1):47–58
Acknowledgements
This study was supported by a grant from the Natural Science Foundation of Heilongjiang Province (C201425).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
The experimental protocol was approved by the Ethics Committee on the Use and Care of Animals, Northeast Agricultural University, China.
Conflict of Interest
The authors declare that they have no conflict of interest.
Rights and permissions
About this article
Cite this article
Sun, X., Sun, H., Yu, K. et al. Aluminum Chloride Causes the Dysfunction of Testes Through Inhibiting the ATPase Enzyme Activities and Gonadotropin Receptor Expression in Rats. Biol Trace Elem Res 183, 296–304 (2018). https://doi.org/10.1007/s12011-017-1120-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12011-017-1120-1