Attenuation potentials of royal jelly against hydroxyurea-induced infertility through inhibiting oxidation and release of pro-inflammatory cytokines in male rats

被引:11
作者
Tohamy, Hossam G. [1 ]
El-Karim, Dina R. Gad [2 ]
El-Sayed, Yasser S. [3 ]
机构
[1] Alexandria Univ, Fac Vet Med, Dept Pathol, Alexandria, Egypt
[2] Alexandria Univ, Fac Vet Med, Dept Clin Pathol, Alexandria, Egypt
[3] Damanhour Univ, Fac Vet Med, Dept Forens Med & Toxicol, Damanhour 22511, Egypt
关键词
Hydroxyurea; Royal jelly; Male infertility; Oxidative damage; Cytokines; Histopathology; SICKLE-CELL-DISEASE; TESTICULAR TOXICITY; LIPID-PEROXIDATION; SPERM PARAMETERS; NITRIC-OXIDE; IN-VITRO; DAMAGE; ACID; SPERMATOGENESIS; TESTOSTERONE;
D O I
10.1007/s11356-019-05521-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hydroxyurea (HDU), a class of antineoplastic drugs, has a powerful efficacy in the treatment of several types of malignancies. However, it has multiple adverse effects including reduced fertility, especially in males. Thus, 60 male albino rats were used to investigate the chemoprotective potentials of royal jelly on HDU-induced testicular damage. Animals were gastro-gavaged with HDU (225 or 450 mg kg(-1) bw day(-1)) before royal jelly (100 mg kg(-1) bw day(-1)) for 60 days. Blood samples and testicles were collected, and spermatozoon was obtained. In a dose-dependent manner, the sperm count, motility and liveability, and testosterone, GSH, and catalase concentrations were decreased in HDU groups, whereas MDA, FSH, LH, IL-6, and IFN-gamma expression levels were increased. Germinal epithelium degeneration, germ cell sloughing, reduction in the number of luminal spermatozoa, interstitial congestion, and severe leukocyte infiltration besides no glandular secretion in most of the acini were identified. However, royal jelly intake in HDU-treated rats successfully improved sperm quality, hormonal and antioxidant status, and reproductive organ histoarchitecture. Thus, it could be concluded that royal jelly is endowed with antioxidative and anti-inflammatory activities and could be, therefore, used as an adjuvant remedy to improve HDU-induced male subfertility.
引用
收藏
页码:21524 / 21534
页数:11
相关论文
共 55 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Hydroxyurea in Sickle Cell Disease: Drug Review [J].
Agrawal, Rohit Kumar ;
Patel, Rakesh Kantilal ;
Shah, Varsha ;
Nainiwal, Lalit ;
Trivedi, Bhadra .
INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2014, 30 (02) :91-96
[3]   Protective role of nimbolide against chemotherapeutic drug hydroxyurea induced genetic and oxidative damage in an animal model [J].
Ahmad, Md Fahim ;
Ansari, Mohd Owais ;
Jameel, Sana ;
Wani, Ab Latif ;
Parveen, Nuzhat ;
Siddique, Hifzur R. ;
Shadab, G. G. H. A. .
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2018, 60 :91-99
[4]  
Amirshahi Tayebeh, 2014, Iran J Reprod Med, V12, P209
[5]   Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males [J].
Berthaut, Isabelle ;
Guignedoux, Geoffroy ;
Kirsch-Noir, Frederique ;
de Larouziere, Vanina ;
Ravel, Celia ;
Bachir, Dora ;
Galacteros, Frederic ;
Ancel, Pierre-Yves ;
Kunstmann, Jean-Marie ;
Levy, Laurence ;
Jouannet, Pierre ;
Girot, Robert ;
Mandelbaum, Jacqueline .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 (07) :988-993
[6]   Adverse effect of hydroxyurea on spermatogenesis in patients with sickle cell anemia after 6 months of treatment [J].
Berthaut, Isabelle ;
Bachir, Dora ;
Kotti, Salma ;
Chalas, Celine ;
Stankovic, Katia ;
Eustache, Florence ;
Ravel, Celia ;
Habibi, Anoosha ;
Brailly-Tabard, Sylvie ;
Levy-Dutel, Laurence ;
Bleibtreu, Alexandre ;
Simon, Tabassome ;
Galacteros, Frederic ;
Lionnet, Francois ;
Mandelbaum, Jacqueline .
BLOOD, 2017, 130 (21) :2354-2356
[7]   Evaluation of the one-step eosin-nigrosin staining technique for human sperm vitality assessment [J].
Björndahl, L ;
Söderlund, I ;
Kvist, U .
HUMAN REPRODUCTION, 2003, 18 (04) :813-816
[8]  
Blanco-Rodríguez J, 1998, INT J ANDROL, V21, P109
[9]   EFFECT OF HYDROXYUREA ON THE FREQUENCY OF PAINFUL CRISES IN SICKLE-CELL-ANEMIA [J].
CHARACHE, S ;
TERRIN, ML ;
MOORE, RD ;
DOVER, GJ ;
BARTON, FB ;
ECKERT, SV ;
MCMAHON, RP ;
BONDS, DR ;
ORRINGER, E ;
JONES, S ;
STRAYHORN, D ;
ROSSE, W ;
PHILLIPS, G ;
PEACE, D ;
JOHNSONTELFAIR, A ;
MILNER, P ;
KUTLAR, A ;
TRACY, A ;
BALLAS, SK ;
ALLEN, GE ;
MOSHANG, J ;
SCOTT, B ;
STEINBERG, M ;
ANDERSON, A ;
SABAHI, V ;
PEGELOW, C ;
TEMPLE, D ;
CASE, E ;
HARRELL, R ;
CHILDERIE, S ;
EMBURY, S ;
SCHMIDT, B ;
DAVIES, D ;
KOSHY, M ;
TALISCHYZAHED, N ;
DORN, L ;
PENDARVIS, G ;
MCGEE, M ;
TELFER, M ;
DAVIS, A ;
CASTRO, O ;
FINKE, H ;
PERLIN, E ;
SITEMAN, J ;
GASCON, P ;
DIPAOLO, P ;
GARGIULO, S ;
ECKMAN, J ;
BAILEY, JH ;
PLATT, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (20) :1317-1322
[10]   In Vitro Anti-Inflammatory Effects of Three Fatty Acids from Royal Jelly [J].
Chen, Yi-Fan ;
Wang, Kai ;
Zhang, Yan-Zheng ;
Zheng, Yu-Fei ;
Hu, Fu-Liang .
MEDIATORS OF INFLAMMATION, 2016, 2016