Santos Thays Cristina Dos, Silva Hellen Paulo, Lima Karen Rodrigues, Salvador Maria Luiza Nonato, Cândido Geraldo de Sousa, Pimenta Laura Cristina Jardim Pôrto, Bertolini Natália Oliveira, Ribeiro Luciana Botelho, Fagundes Filipe Gomes, Orlando Débora Ribeiro, Borges Bruno Del Bianco, Dias-Peixoto Marco Fabrício, Machado Alan Rodrigues Teixeira, Dobbss Leonardo Barros, Pereira Luciano José, Andrade Eric Francelino
Faculty of Health Sciences, Universidade Federal de Lavras (UFLA), Lavras 37200-000, Minas Gerais, Brazil.
Department of Physical Education, University Center of Lavras (UNILAVRAS), Lavras 37200-000, Minas Gerais, Brazil.
Biomedicines. 2025 Feb 17;13(2):495. doi: 10.3390/biomedicines13020495.
Estrogen depletion alters bone mineralization and oxidative stress. Antioxidants like humic acids (HA) may help mitigate bone demineralization and redox imbalances. Thus, this study evaluated the effects of HA on bone mineral composition and oxidative stress markers in an experimental menopause model. Twenty-four female C57BL/6 mice were divided into four groups (n = 6/group): Sham; Sham + HA; Ovariectomized (OVX); and OVX + HA. The menopause model was induced by bilateral ovariectomy at the beginning of the experiment. HA derived from biomass vermicompost was administered daily by gavage for 28 days. After euthanasia, femurs and fragments of the gastrocnemius muscle, liver, and kidney were collected. Bone elemental composition was analyzed using scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy (EDS). Superoxide dismutase (SOD), catalase (CAT), and hydrogen peroxide (HO) activities were assessed in muscle, renal, and hepatic tissues. Data were analyzed using two-way ANOVA and Bonferroni's post hoc test. Untreated OVX mice exhibited a significant reduction in femoral calcium content ( < 0.05). However, HA treatment increased calcium levels and improved the Ca/P ratio ( < 0.05). HO activity was reduced in the liver and kidney of OVX + HA mice compared to untreated animals ( < 0.05). CAT activity in muscle increased in the OVX + HA group compared to the OVX ( < 0.05). HA treatment improved femoral elemental composition and modulated oxidative stress markers in an experimental menopause model.
雌激素缺乏会改变骨矿化和氧化应激。腐殖酸(HA)等抗氧化剂可能有助于减轻骨质脱矿和氧化还原失衡。因此,本研究在实验性绝经模型中评估了HA对骨矿物质组成和氧化应激标志物的影响。将24只雌性C57BL/6小鼠分为四组(每组n = 6):假手术组;假手术 + HA组;卵巢切除(OVX)组;以及OVX + HA组。在实验开始时通过双侧卵巢切除术诱导绝经模型。源自生物质蚯蚓堆肥的HA每天通过灌胃给药,持续28天。安乐死后,收集股骨以及腓肠肌、肝脏和肾脏的组织碎片。使用扫描电子显微镜(SEM)结合能量色散光谱(EDS)分析骨元素组成。评估肌肉、肾脏和肝脏组织中的超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和过氧化氢(HO)活性。使用双向方差分析和Bonferroni事后检验分析数据。未治疗的OVX小鼠股骨钙含量显著降低(<0.05)。然而,HA治疗增加了钙水平并改善了钙/磷比值(<0.05)。与未治疗的动物相比,OVX + HA小鼠肝脏和肾脏中的HO活性降低(<0.05)。与OVX组相比,OVX + HA组肌肉中的CAT活性增加(<0.05)。HA治疗改善了实验性绝经模型中的股骨元素组成并调节了氧化应激标志物。