Department of Surgery and Faculty of Kinesiology, University of Calgary, Calgary, AB T2N 4N1, Canada.
Bone & Joint Health Strategic Clinical Network, Alberta Health Services, Edmonton, AB T5J 3E4, Canada.
Int J Mol Sci. 2022 Apr 8;23(8):4119. doi: 10.3390/ijms23084119.
Sex-specific differences in biology and physiology likely start at the time of conception and progress and mature during the pre-puberty time frame and then during the transitions accompanying puberty. These sex differences are impacted by both genetics and epigenetic alterations during the maturation process, likely for the purpose of preparing for successful reproduction. For females, later in life (~45-50) they undergo another transition leading to a loss of ovarian hormone production at menopause. The reasons for menopause are not clear, but for a subset of females, menopause is accompanied by an increased risk of a number of diseases or conditions that impact a variety of tissues. Most research has mainly focused on the target cells in each of the affected tissues rather than pursue the alternative option that there may be commonalities in the development of these post-menopausal conditions in addition to influences on specific target cells. This review will address some of the potential commonalities presented by an integration of the literature regarding tissue-specific aspects of these post-menopausal conditions and data presented by space flight/microgravity (a condition not anticipated by evolution) that could implicate a loss of a regulatory function of the microvasculature in the risk attached to the affected tissues. Thus, the loss of the integration of the paracrine relationships between endothelial cells of the microvasculature of the tissues affected in the post-menopausal environment could contribute to the risk for post-menopausal diseases/conditions. The validation of this concept could lead to new approaches for interventions to treat post-menopausal conditions, as well as provide new understanding regarding sex-specific biological regulation.
生物学和生理学上的性别特异性差异可能在受孕时开始,并在青春期前的阶段发展和成熟,然后在伴随青春期的转变过程中进一步发展。这些性别差异受到遗传和表观遗传改变的影响,这可能是为了为成功繁殖做准备。对于女性来说,在生命的后期(约 45-50 岁),她们会经历另一次转变,导致更年期时卵巢激素产生丧失。更年期的原因尚不清楚,但对于一部分女性来说,更年期伴随着许多疾病或状况的风险增加,这些疾病或状况会影响多种组织。大多数研究主要集中在受影响组织中的靶细胞上,而不是考虑除了对特定靶细胞的影响之外,这些绝经后状况的发展可能还有共同之处这一替代选择。本综述将讨论一些潜在的共性,这些共性是通过整合关于这些绝经后状况的组织特异性方面的文献和太空飞行/微重力(一种进化没有预料到的情况)的数据提出的,这可能意味着受影响组织中小血管的调节功能丧失。因此,受影响组织中小血管内皮细胞的旁分泌关系的整合丧失可能导致绝经后疾病/状况的风险增加。这一概念的验证可能为绝经后疾病的治疗提供新的干预方法,并提供关于性别特异性生物学调节的新认识。