Departments of Physical Therapy and Rehabilitation Science, University of Iowa, Iowa City, Iowa, 52242.
Neuroscience and Pharmacology, University of Iowa, Iowa City, Iowa, 52242.
eNeuro. 2024 Aug 28;11(8). doi: 10.1523/ENEURO.0332-24.2024. Print 2024 Aug.
Animal studies consistently demonstrate that testosterone is protective against pain in multiple models, including an animal model of activity-induced muscle pain. In this model, females develop widespread muscle hyperalgesia, and reducing testosterone levels in males results in widespread muscle hyperalgesia. Widespread pain is believed to be mediated by changes in the central nervous system, including the rostral ventromedial medulla (RVM). The enzyme that converts testosterone to estradiol, aromatase, is highly expressed in the RVM. Therefore, we hypothesized that testosterone is converted by aromatase to estradiol locally in the RVM to prevent development of widespread muscle hyperalgesia in male mice. This was tested through pharmacological inhibition of estrogen receptors (ERs), aromatase, or ER-α in the RVM which resulted in contralateral hyperalgesia in male mice (C57BL/6J). ER inhibition in the RVM had no effect on hyperalgesia in female mice. As prior studies show modulation of estradiol signaling alters GABA receptor and transporter expression, we examined if removal of testosterone in males would decrease mRNA expression of GABA receptor subunits and vesicular GABA transporter (VGAT). However, there were no differences in mRNA expression of GABA receptor subunits of VGAT between gonadectomized and sham control males. Lastly, we used RNAscope to determine expression of ER-α in the RVM and show expression in inhibitory (VGAT+), serotonergic (tryptophan hydroxylase 2+), and μ-opioid receptor expressing (MOR+) cells. In conclusion, testosterone protects males from development of widespread hyperalgesia through aromatization to estradiol and activation of ER-α which is widely expressed in multiple cell types in the RVM.
动物研究一致表明,睾丸酮在多种模型中具有保护作用,可以缓解疼痛,包括活动引起的肌肉疼痛模型。在该模型中,雌性动物会出现广泛的肌肉痛觉过敏,而雄性动物睾丸酮水平降低会导致广泛的肌肉痛觉过敏。广泛的疼痛被认为是由中枢神经系统的变化介导的,包括吻侧腹内侧髓质(RVM)。将睾丸酮转化为雌二醇的酶,即芳香酶,在 RVM 中高度表达。因此,我们假设睾丸酮在 RVM 中被芳香酶转化为雌二醇,以防止雄性小鼠出现广泛的肌肉痛觉过敏。这通过在 RVM 中抑制雌激素受体(ERs)、芳香酶或 ER-α来测试,结果导致雄性小鼠出现对侧痛觉过敏(C57BL/6J)。在 RVM 中抑制 ER 对雌性小鼠的痛觉过敏没有影响。由于先前的研究表明雌二醇信号的调节会改变 GABA 受体和转运体的表达,我们检查了雄性小鼠去势是否会降低 GABA 受体亚单位和囊泡 GABA 转运体(VGAT)的 mRNA 表达。然而,去势雄性和假手术对照雄性之间的 GABA 受体亚单位和 VGAT 的 mRNA 表达没有差异。最后,我们使用 RNAscope 确定了 RVM 中 ER-α的表达,并显示其在抑制性(VGAT+)、5-羟色胺能(色氨酸羟化酶 2+)和μ-阿片受体表达(MOR+)细胞中表达。总之,睾丸酮通过芳香化为雌二醇和激活广泛表达于 RVM 中多种细胞类型的 ER-α,来保护雄性免受广泛痛觉过敏的发展。