Department of General Biology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil; Department of Animal Biology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Department of General Biology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil; Institut national de la santé et de la recherche médicale (Inserm), Institut de recherche en santé, environnement et travail (Irset), Université de Rennes 1, UMR 1085 Rennes, France.
J Trace Elem Med Biol. 2023 Dec;80:127271. doi: 10.1016/j.jtemb.2023.127271. Epub 2023 Jul 25.
Some residues such as the heavy metals cadmium (Cd), lead (Pb), chromium (Cr VI), nickel (Ni), and arsenic (As), this last one in its oxidized forms + 5 (arsenate) and + 3 (arsenite), can cause injuries to human health, so they are currently considered environmental health emergencies. In the testis, heavy metals can cause morphological and functional damage due to constant exposure acting chronically in individuals. Thus, we aimed to determine the toxicological mechanism of As, As, Cd, Cr VI, and Ni that leads to testicular damage and establish for the first time an order of toxicity among these studied heavy metals.
Forty-two Swiss mice at reproductive age (140 days) were used, randomly distributed into seven experimental groups (n = 6). Exposure to heavy metals was weekly performed, by intraperitoneal route. Group 1 received 0.7 mL 0.9% saline (control), and the other groups received 1.5 mg/ kg of As, As, Cd, Pb, Cr VI, or Ni, for six weeks.
These studied heavy metals did not accumulate in the testis tissue. However, exposure to Ni induced moderate pathologies in the seminiferous tubules, plus changes in the tunica propria, blood vessels, lymphatic space, and carbonyl protein levels. Cd exposure caused moderate tubular histopathologies and changes in the blood vessels and lymphatic space. Cr VI induced slight tubular histopathologies, changes in the lymphatic space, blood vessels, and SOD activity. Pb and As exposure triggered moderate tubular pathologies and changes in the SOD activity and carbonyl protein levels, respectively. Finally, As induced only slight tubular pathologies.
The testicular histopathologies caused by the studied heavy metals are mainly triggered by changes in testicular oxidative balance. Based on our findings of histomorphological alterations, the toxicity order among the heavy metals is Ni>Cd>Cr(VI)>PbAs >As. However, considering oxidative stress results, we propose the following testicular toxicity order for these heavy metals: Ni>As > Cd>Cr(VI)>Pb>As. Ni exposure shows the most harmful among the heavy metals to the testis.
一些残留物,如重金属镉(Cd)、铅(Pb)、铬(Cr VI)、镍(Ni)和砷(As),最后一种以其氧化形式+5(砷酸盐)和+3(亚砷酸盐)存在,会对人类健康造成伤害,因此它们目前被认为是环境健康紧急情况。在睾丸中,由于重金属在个体中持续慢性暴露,会导致形态和功能损伤。因此,我们旨在确定导致睾丸损伤的砷、砷、镉、Cr VI 和 Ni 的毒理学机制,并首次确定这些研究中的重金属的毒性顺序。
使用 42 只处于生殖期(140 天)的瑞士小鼠,随机分为七组(n=6)。每周通过腹腔途径暴露于重金属。第 1 组接受 0.7mL 0.9%生理盐水(对照),其他组接受 1.5mg/kg 的砷、砷、镉、铅、Cr VI 或 Ni,共 6 周。
这些研究中的重金属并未在睾丸组织中积累。然而,暴露于 Ni 会导致生精小管发生中度病理变化,同时还会改变固有层、血管、淋巴空间和羰基蛋白水平。Cd 暴露会导致中度管状组织病理学变化,并改变血管和淋巴空间。Cr VI 诱导轻微的管状组织病理学变化,改变淋巴空间、血管和 SOD 活性。Pb 和 As 暴露分别触发中度管状病理学变化以及 SOD 活性和羰基蛋白水平的改变。最后,As 仅诱导轻微的管状病理学变化。
研究中重金属引起的睾丸组织病理学变化主要是由睾丸氧化平衡的变化引起的。基于我们对组织形态学改变的发现,重金属的毒性顺序为 Ni>Cd>Cr(VI)>PbAs >As。然而,考虑到氧化应激的结果,我们提出这些重金属对睾丸的毒性顺序为:Ni>As >Cd>Cr(VI)>Pb>As。Ni 暴露在这些重金属中对睾丸的危害最大。