RETRACTED: Research Article Flavocoxid Protects Against Cadmium-Induced Disruption of the Blood-Testis Barrier and Improves Testicular Damage and Germ Cell Impairment in Mice (Retracted article. See vol. 190, pg. 110, 2022)

被引:48
作者
Minutoli, Letteria [1 ]
Micali, Antonio [2 ]
Pisani, Antonina [2 ]
Puzzolo, Domenico [2 ]
Bitto, Alessandra [1 ]
Rinaldi, Mariagrazia [1 ]
Pizzino, Gabriele [1 ]
Irrera, Natasha [1 ]
Galfo, Federica [1 ]
Arena, Salvatore [3 ]
Pallio, Giovanni [1 ]
Mecchio, Anna [1 ]
Germana, Antonino [4 ]
Bruschetta, Daniele [2 ]
Laura, Rosaria [5 ]
Magno, Carlo [6 ]
Marini, Herbert [1 ]
Squadrito, Francesco [1 ]
Altavilla, Domenica [3 ]
机构
[1] Univ Messina, Dept Clin & Expt Med, Messina, Italy
[2] Univ Messina, Dept Biomed Sci & Morphol & Funct Images, Messina, Italy
[3] Univ Messina, Dept Paediat Gynaecol Microbiol & Biomed Sci, Messina, Italy
[4] Univ Messina, Dept Vet Sci, Messina, Italy
[5] Univ Messina, Dept Biol & Environm Sci, Messina, Italy
[6] Univ Messina, Dept Human Pathol, Messina, Italy
关键词
flavocoxid; seminiferous tubules; germ cells; p-ERK; 1/2; TNF-alpha; light microscopy; SEMINIFEROUS EPITHELIUM; OXIDATIVE STRESS; DUAL INHIBITOR; EXPRESSION; 5-LIPOXYGENASE; CYCLOOXYGENASE-2; PERMEABILITY; INVOLVEMENT; INFERTILITY; MECHANISM;
D O I
10.1093/toxsci/kfv185
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cadmium (Cd) causes male infertility. There is the need to identify safe treatments counteracting this toxicity. Flavocoxid is a flavonoid that induces a balanced inhibition of cyclooxygenase (COX)-1 and COX-2 peroxidase moieties and of 5-lipoxygenase (LOX) and has efficacy in the male genitourinary system. We investigated flavocoxid effects on Cd-induced testicular toxicity in mice. Swiss mice were divided into 4 groups: 2 control groups received 0.9% NaCl (vehicle; 1 ml/kg/day) or flavocoxid (20 mg/kg/day ip); 2 groups were challenged with cadmium chloride (CdCl2; 2 mg/kg/day ip) and administered with vehicle or flavocoxid. The treatment lasted for 1 or 2 weeks. The testes were processed for biochemical and morphological studies. CdCl2 increased phosphorylated extracellular signal-regulated kinase (p-ERK) 1/2, tumor necrosis factor (TNF)-alpha, COX-2, 5-LOX, malondialdehyde (MDA), B-cell-lymphoma (Bcl)-2-associated X protein (Bax), follicle-stimulating hormone (FSH), luteinizing hormone (LH), transforming growth factor (TGF) -beta 3, decreased Bcl-2, testosterone, inhibin-B, occludin, N-Cadherin, induced structural damages in the testis and disrupted the blood-testis barrier. Many TUNEL-positive germ cells and changes in claudin-11, occludin, and N-cadherin localization were present. Flavocoxid administration reduced, in a time-dependent way, p-ERK 1/2, TNF-alpha, COX-2, 5-LOX, MDA, Bax, FSH, LH, TGF-beta 3, augmented Bcl-2, testosterone, inhibin B, occludin, N-Cadherin, and improved the structural organization of the testis and the blood-testis barrier. Few TUNEL-positive germ cells were present and a morphological retrieval of the intercellular junctions was observed. In conclusion, flavocoxid has a protective anti-inflammatory, antioxidant, and antiapoptotic function against Cd-induced toxicity in mice testis. We suggest that flavocoxid may play a relevant positive role against environmental levels of Cd, otherwise deleterious to gametogenesis and tubular integrity.
引用
收藏
页码:311 / 329
页数:19
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