Faculty of Medicine, Department of Physiology, Institute of Cardiovascular Sciences, St. Boniface Hospital Research, Winnipeg, Canada.
J Cell Physiol. 2011 Jan;226(1):181-6. doi: 10.1002/jcp.22321.
This study was undertaken to determine alterations in the β-adrenoceptor (β-AR) signaling system in male and female rats at 4 weeks after the induction of arteriovenous (AV) fistula or shunt. AV shunt produced a greater degree of cardiac hypertrophy and larger increase in cardiac output in male than in female animals. Increases in plasma levels of norepinephrine and epinephrine (EPI) due to AV shunt were also higher in male than females. While no difference in the β(1)-AR affinity was seen in males and females, AV shunt induced increase in β(1)-AR density in female rats was higher than that in males. Furthermore, no changes in basal adenylyl cyclase (AC) V/VI mRNA levels were seen; however, the increase in EPI-stimulated AC activities was greater in AV shunt females than in males. AV shunt decreased myocardial β(1)-AR mRNA level in male rats and increased β(2)-AR mRNA level in female hearts; an increase in G(i)-protein mRNA was detected only in male hearts. Although GRK2 gene expression was increased in both sexes, an increase in GRK3 mRNA was seen only in AV shunt female rats. β-arrestin1 mRNA was elevated in females whereas β-arrestin 2 gene expression was increased in both male and female AV shunt rats. While these data demonstrate gender associated differences in various components of the β-AR system in cardiac hypertrophy due to AV shunt, only higher levels of plasma catecholamines may account for the greater increase in cardiac output and higher degree of cardiac hypertrophy in males.
本研究旨在确定动静脉(AV)瘘或分流后 4 周雄性和雌性大鼠β-肾上腺素能受体(β-AR)信号系统的变化。AV 分流在雄性动物中引起更大程度的心脏肥大和心输出量增加,而在雌性动物中则更大。由于 AV 分流,雄性动物血浆去甲肾上腺素和肾上腺素(EPI)水平的升高也高于雌性动物。虽然雄性和雌性之间β(1)-AR 亲和力没有差异,但 AV 分流诱导的雌性大鼠β(1)-AR 密度增加高于雄性。此外,基础腺苷酸环化酶(AC)V/VI mRNA 水平没有变化;然而,AV 分流雌性的 EPI 刺激 AC 活性增加大于雄性。AV 分流降低了雄性大鼠心肌β(1)-AR mRNA 水平,增加了雌性心脏β(2)-AR mRNA 水平;仅在雄性心脏中检测到 G(i)-蛋白 mRNA 的增加。尽管 GRK2 基因表达在两性中均增加,但仅在 AV 分流雌性大鼠中观察到 GRK3 mRNA 的增加。β-arrestin1 mRNA 在雌性中升高,而β-arrestin 2 基因表达在雄性和雌性 AV 分流大鼠中均增加。虽然这些数据表明由于 AV 分流导致心脏肥大的β-AR 系统的各种成分存在性别相关差异,但只有更高水平的血浆儿茶酚胺才能解释男性心输出量增加和心脏肥大程度更高的原因。