Department of Integrative Physiology, and Cardiovascular Research Institute, University of North Texas Health Science Centre at Fort Worth, Fort Worth, TX 76107, USA.
J Neuroendocrinol. 2012 Apr;24(4):642-52. doi: 10.1111/j.1365-2826.2011.02273.x.
The present study aimed to measure the expression of transient receptor potential (TRP) channels in the magnocellular neurones of the paraventricular (PVN) and supraoptic nucleus (SON) in an animal model of hepatic cirrhosis associated with inappropriate vasopressin (AVP) release. In these studies, we used chronic bile duct ligation (BDL) in the rat, which is a commonly used model of hepatic cirrhosis, associated with elevated plasma AVP. The present study tested the hypothesis that changes in TRP vanilloid (TRPV) channel expression may be related to inappropriate AVP release in BDL rats. To test our hypothesis, we utilised laser capture microdissection of AVP neurones in the PVN and SON and western blot analysis from brain punches. Laser capture microdissection and quantitative reverse transcriptase-polymerase chain reaction demonstrated elevated TRPV2 mRNA in the PVN and SON of BDL compared to sham-ligated controls. AVP transcription was also increased as determined using intron specific primers to measure heteronuclear RNA. Immunohistochemistry demonstrated increased AVP and TRPV2 positive cells in both the PVN and SON after BDL. Also, there was an increased co-expression of TRPV2 and AVP cells after BDL. However, there was no change in the colocalisation counts of TRPV2 and oxytocin in both the magnocellular regions evaluated. In the SON but not the PVN, the transcription levels of TRPV4 were also significantly increased in BDL rats. Western blot analysis of punches containing the PVN and SON revealed that TRPV2 protein content was significantly increased in these brain regions in BDL rats compared to sham rats. Our data suggest that regionally specific changes in TRPV expression in the magnocellular neurosecretory cell AVP neurones could alter their osmosensing ability.
本研究旨在测量在与不适当血管加压素 (AVP) 释放相关的肝硬变动物模型中,室旁核 (PVN) 和视上核 (SON) 的大细胞神经元中瞬时受体电位 (TRP) 通道的表达。在这些研究中,我们使用慢性胆管结扎 (BDL) 作为大鼠肝硬变的常用模型,其与升高的血浆 AVP 相关。本研究检验了以下假说:TRP 香草素 (TRPV) 通道表达的变化可能与 BDL 大鼠中不适当的 AVP 释放有关。为了验证我们的假说,我们利用 PVN 和 SON 中 AVP 神经元的激光捕获显微解剖和脑穿刺的 Western blot 分析。激光捕获显微解剖和定量逆转录聚合酶链反应显示,与 sham 结扎对照组相比,BDL 大鼠的 PVN 和 SON 中 TRPV2 mRNA 升高。使用异核 RNA 测量的内含子特异性引物也表明 AVP 转录增加。免疫组织化学显示,BDL 后 PVN 和 SON 中 AVP 和 TRPV2 阳性细胞增加。此外,BDL 后 TRPV2 和 AVP 细胞的共表达也增加。然而,在评估的两个大细胞区域中,TRPV2 和催产素的共定位计数没有变化。在 SON 中,但不在 PVN 中,BDL 大鼠的 TRPV4 转录水平也显著增加。包含 PVN 和 SON 的脑穿刺的 Western blot 分析显示,与 sham 大鼠相比,BDL 大鼠这些脑区的 TRPV2 蛋白含量显著增加。我们的数据表明,大细胞神经分泌细胞 AVP 神经元中 TRPV 表达的区域特异性变化可能改变其渗透压感知能力。