Tham M, Sim M K, Tang F R
Department of Pharmacology, Faculty of Medicine, National University of Singapore, 119260, Singapore, Singapore.
Regul Pept. 2001 Sep 15;101(1-3):51-7. doi: 10.1016/s0167-0115(01)00260-9.
The renin-angiotensin system (RAS) in the hypoglossal nuclei of the rat was studied by immunohistochemistry. Antibodies to angiotensin AT(1) receptor (AT1), angiotensinogen (ANG), renin (REN), angiotensin converting enzyme (ACE) and angiotensin II (AII) were used. All the components of the RAS with the exception of renin were detected. Light and electron microscopy revealed the following results: ANG was predominantly found in astrocytes, with small amounts in neuronal dendrites; ACE was found in the cytoplasm of neurons, dendrites and astrocyte processes; AT1 was found in the cytoplasm of neurons and dendrites, but not on the membrane; and AII was found mainly in astrocytes with some located in the dendrites and cytoplasm. Right hypoglossal nerve lesion caused an increase in expression of AT1 in neurons as early as 2 days post-lesion. An increase in expression of ANG in astrocytes was also seen, but at a much later time of 3 weeks post-lesion. For AII, staining occurred in both the neurons and astrocytes in the undamaged hypoglossal nucleus. Nerve lesion caused a disappearance of neuronal stains and an increase in astrocyte stains. There were no changes in ACE staining after nerve lesion. We speculate that ANG and AII are made within the astrocytes, whereas ACE could either be uptaken from blood or de novo synthesized. AT1 may potentially be internal soluble receptors. As to the function of AII in the hypoglossal nucleus, the data do not support AII as a neurotransmitter in the hypoglossal nucleus. It may function as a neuromodulator and also be involved in basic cellular activities, e.g. regulation of transcription factors.
采用免疫组织化学方法对大鼠舌下神经核中的肾素-血管紧张素系统(RAS)进行了研究。使用了针对血管紧张素AT(1)受体(AT1)、血管紧张素原(ANG)、肾素(REN)、血管紧张素转换酶(ACE)和血管紧张素II(AII)的抗体。除肾素外,RAS的所有成分均被检测到。光镜和电镜检查结果如下:ANG主要存在于星形胶质细胞中,少量存在于神经元树突中;ACE存在于神经元、树突和星形胶质细胞突起的细胞质中;AT1存在于神经元和树突的细胞质中,但不在细胞膜上;AII主要存在于星形胶质细胞中,部分存在于树突和细胞质中。右侧舌下神经损伤后,早在损伤后2天,神经元中AT1的表达就增加。星形胶质细胞中ANG的表达也增加,但在损伤后3周的较晚时间。对于AII,在未受损的舌下神经核的神经元和星形胶质细胞中均有染色。神经损伤导致神经元染色消失,星形胶质细胞染色增加。神经损伤后ACE染色无变化。我们推测ANG和AII是在星形胶质细胞内产生的,而ACE可能是从血液中摄取或重新合成的。AT1可能是潜在的内部可溶性受体。至于AII在舌下神经核中的功能,数据不支持AII作为舌下神经核中的神经递质。它可能作为神经调节剂发挥作用,也参与基本的细胞活动,如转录因子的调节。