Jean-Faucher C, Berger M, Gallon C, de Turckheim M, Veyssière G, Jean C
Physiologie Comparée et Endocrinologie, CNRS UA 360, Université de Clermont II, Aubière, France.
J Endocrinol. 1987 Nov;115(2):241-6. doi: 10.1677/joe.0.1150241.
Kidneys of adult male mice are larger than those of females because of both cellular hyperplasia and hypertrophy. Administration of testosterone to adult female mice induced cellular hypertrophy but not hyperplasia, so that the weight of the kidney remained smaller than in male mice. The sexual dimorphism in kidney size is not congenital but programmed by neonatal endogenous androgens and expressed between 30 and 40 days of age. Treatment of newborn males with cyproterone acetate and of newborn females with testosterone induced female and male patterns of renal growth respectively. It appears that neonatal endogenous androgens are required to induce the characteristic cellular hyperplasia of the kidneys of male mice. Manipulation of androgen levels during neonatal and prepubertal life was found to affect the growth response of the kidney to androgens in adult male and female mice.
成年雄性小鼠的肾脏比雌性小鼠的大,这是由于细胞增生和肥大共同作用的结果。给成年雌性小鼠注射睾酮会诱导细胞肥大,但不会导致细胞增生,因此其肾脏重量仍比雄性小鼠的小。肾脏大小的性别差异并非先天性的,而是由新生儿内源性雄激素编程,并在30至40日龄时表现出来。用醋酸环丙孕酮治疗新生雄性小鼠,用睾酮治疗新生雌性小鼠,分别诱导出雌性和雄性的肾脏生长模式。看来,新生儿内源性雄激素是诱导雄性小鼠肾脏特征性细胞增生所必需的。研究发现,在新生儿期和青春期前对雄激素水平进行调控,会影响成年雄性和雌性小鼠肾脏对雄激素的生长反应。