de Sousa Júlia Ingryd Targino, Gonçalves Juliana de Lima, de Queiroz Alexandra Mussolino, de Carvalho Fabrício Kitazono, de Paula-Silva Francisco Wanderley Garcia
Department of Pediatric Dentistry, Ribeirão Preto School of Dentistry, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
PLoS One. 2024 Dec 19;19(12):e0315667. doi: 10.1371/journal.pone.0315667. eCollection 2024.
Dental development is a complex process influenced by genetic and environmental factors. Dental enamel, primarily composed of hydroxyapatite, is formed through complex cellular and biochemical mechanisms. Although this is a stable process, genetic, nutritional, and environmental factores can lead to developmental defects such as hypomineralization and hypoplasia. Molar incisor hypomineralization is a type of hypomineralization that represents a public health challenge. Its etiology is not yet fully understood, but factors such as hypoxia, medication exposure, adverse events in early childhood, and genetic influences are considered. This study protocol aims to investigate whether postnatal adverse events can impact amelogenesis, exploring the role of stress in the etiology of dental enamel defects. Specific objectives include evaluating enamel structure and mechanical properties by comparing the offspring of rats exposed to postnatal maternal separation with control animals (non-exposed). Additionally, we will evaluate weight, length, survival assessment, and developmental milestones between the groups. Macrophotographic analysis, microtomography, microhardness testing, and electron microscopy will enable a detailed assessment of enamel morphology and its mechanical properties. Histological and molecular analyses-such as immunohistochemistry, indirect immunofluorescence, and in situ zymography-will be performed to evaluate possible changes in proteins and enzymes that are essential for proper enamel biomineralization.
牙齿发育是一个受遗传和环境因素影响的复杂过程。牙釉质主要由羟基磷灰石组成,通过复杂的细胞和生化机制形成。尽管这是一个稳定的过程,但遗传、营养和环境因素可导致发育缺陷,如矿化不足和发育不全。磨牙切牙矿化不足是一种矿化不足类型,是一个公共卫生挑战。其病因尚未完全了解,但诸如缺氧、药物暴露、幼儿期不良事件和遗传影响等因素被考虑在内。本研究方案旨在调查出生后不良事件是否会影响釉质形成,探索应激在牙釉质缺陷病因中的作用。具体目标包括通过比较出生后经历母体分离的大鼠后代与对照动物(未暴露)来评估釉质结构和力学性能。此外,我们将评估两组之间的体重、体长、生存评估和发育里程碑。宏观摄影分析、显微断层扫描、显微硬度测试和电子显微镜将能够详细评估釉质形态及其力学性能。将进行组织学和分子分析,如免疫组织化学、间接免疫荧光和原位酶谱分析,以评估对正常釉质生物矿化至关重要的蛋白质和酶的可能变化。