Trejo-Sánchez Itztli, Pérez-Monter Carlos, Huerta-Pacheco Sofía, Gutiérrez-Ospina Gabriel
Laboratorio de Biología de Sistemas, Instituto de Investigaciones Biomédicas, Departamento de Biología Celular y Fisiología, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Programa de Doctorado en Ciencias Biomédicas, Unidad de Posgrado, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Front Behav Neurosci. 2020 Jun 26;14:90. doi: 10.3389/fnbeh.2020.00090. eCollection 2020.
Distinct manifestations of sexual behavior are conceived as separate phenotypes. Each sexual phenotype is assumed to be associated with a characteristic brain. These notions have justified the phenotyping of heterosexual copulator males based upon their ejaculation's latencies (EL) or frequencies (i.e., cumulative ejaculation number; EN). For instance, men and male rats showing premature, normal or retarded ejaculation are assumed to be distinctive endophenotypes. This concept, nonetheless, contradicts past and recent evidence that supports that sexual behavior is highly variable within each sex, and that the brain sexual functional morphology represents an intricate sexual phenotypic mosaic. Hence, for ejaculatory male endophenotypes to be considered as a valid biological concept, it must show internal consistency at various levels of organization (including genetic architectures), after being challenged by intrinsic and/or extrinsic factors. We then judged the internal consistency of the presumed ejaculatory endophenotypes by assessing whether copulatory behavior and the expression of copulation relevant genes and brain limbic structures are specific to each of the presumed EL- or EN-ejaculatory endophenotypes. To do this, copulating male rats were first phenotyped in groups consistently displaying short, average or long ejaculation latencies or very high, high, average, low or very low EN, based in their copulatory performance. Then, the internal consistency of the presumed EL- or EN-endophenotypes was tested by introducing as covariates of phenotyping other copulatory parameters (e.g., number of intromissions) in addition to EL or EN, or by analyzing the expression levels of genes encoding for estrogen receptor alpha, progesterone receptor, androgen receptor, aromatase, DNA methyl-transferase 3a and DNA methyl-transferase 1 in the amygdala, medial preoptic area, ventromedial hypothalamus and olfactory bulb. We found that even though there were group-level differences in all the variables that were studied, these differences did not add-up to create the presumed EL- or EN-ejaculatory endophenotypes. In fact, the extensive overlapping of copulatory parameters and expression levels of copulation relevant genes in limbic structures across EL- or EN-phenotyped copulating male rats, is not consistent with the hypothesis that distinct ejaculatory endophenotypes exist and that they are associated with specific brain characteristics.
性行为的不同表现被视为不同的表型。每种性表型都被认为与特定的大脑相关。这些观念为基于异性交配雄性射精潜伏期(EL)或频率(即累积射精次数;EN)对其进行表型分析提供了依据。例如,表现出早泄、正常射精或射精延迟的男性和雄性大鼠被认为是不同的内表型。然而,这一概念与过去和最近的证据相矛盾,这些证据支持性行为在每个性别中具有高度变异性,并且大脑性功能形态代表了一个复杂的性表型镶嵌体。因此,要使射精雄性内表型被视为一个有效的生物学概念,在受到内在和/或外在因素挑战后,它必须在各个组织水平(包括遗传结构)上显示出内部一致性。然后,我们通过评估交配行为以及与交配相关基因和大脑边缘结构的表达是否特定于每种假定的EL或EN射精内表型,来判断假定的射精内表型的内部一致性。为此,首先根据交配表现将正在交配的雄性大鼠分为持续表现出短、平均或长射精潜伏期或非常高、高、平均、低或非常低的EN的组,对其进行表型分析。然后,通过引入除EL或EN之外的其他交配参数(如插入次数)作为表型分析的协变量,或者通过分析杏仁核、内侧视前区、腹内侧下丘脑和嗅球中编码雌激素受体α、孕激素受体、雄激素受体、芳香化酶、DNA甲基转移酶3a和DNA甲基转移酶1的基因的表达水平,来测试假定的EL或EN内表型的内部一致性。我们发现,尽管在所有研究的变量中存在组水平差异,但这些差异并未累加形成假定的EL或EN射精内表型。事实上,在EL或EN表型的交配雄性大鼠中,交配参数和边缘结构中与交配相关基因的表达水平广泛重叠,这与存在不同射精内表型且它们与特定大脑特征相关的假设不一致。