Schindler M, Holloway S, Hathway G, Woolf C J, Humphrey P P, Emson P C
Glaxo Institute of Applied Pharmacology, Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QJ, UK.
Brain Res. 1998 Jul 6;798(1-2):25-35. doi: 10.1016/s0006-8993(98)00361-8.
Somatostatin is a neuromodulator and neurotransmitter in the central nervous system. Administration of somatostatin to the spinal cord or brain areas involved in nociception has been shown to result in analgesia. Little information is available about the somatostatin receptor types which may be involved in mediating the neuromodulatory and analgesic effects of the peptide. To define the neuronal systems expressing the sst2(a) receptor in brain areas associated with analgesia, immunohistochemical co-localisation studies were carried out in the periaqueductal grey (PAG) and spinal cord using an antibody specific for the sst2(a) receptor. To further define sst2(a) receptor expressing neurones, sst2(a) receptor immunohistochemistry was combined with retrograde tracing using fluorogold. In the PAG, sst2(a) receptor expressing neurones were found to co-express calbindin D28k (36%), the glutamate transporter EAAC-1 (25%), and GABA transporter GAT-1 ( approximately 10%). A total of 65% of sst2(a) positive neurones projected to the thalamus. In the spinal cord, the sst2(a) receptor shows cellular co-localisation with EAAC-1 and GAT-1. Immunohistochemistry and receptor autoradiography using [125I]BIM 23027 after dorsal rhizotomy of the lumbar dorsal roots, L4 and L5, suggests that the somatostatin sst2(a) receptor is not present on primary afferent neurones. Dorsal hemisections of the mid thoracic cord did not alter the immunohistochemical signal for the somatostatin sst2(a) receptor, providing further evidence for an intrinsic localisation of the receptor protein in the dorsal horn of the spinal cord. These data show that the somatostatin sst2(a) receptor exists on morphologically and neurochemically heterogenous neurones and is closely associated with brain areas involved in analgesia and the modulation of nociception.
生长抑素是中枢神经系统中的一种神经调质和神经递质。已证明向参与痛觉感受的脊髓或脑区给予生长抑素会产生镇痛作用。关于可能参与介导该肽的神经调节和镇痛作用的生长抑素受体类型的信息很少。为了确定在与镇痛相关的脑区中表达sst2(a)受体的神经元系统,使用针对sst2(a)受体的特异性抗体在导水管周围灰质(PAG)和脊髓中进行了免疫组织化学共定位研究。为了进一步确定表达sst2(a)受体的神经元,将sst2(a)受体免疫组织化学与使用荧光金的逆行追踪相结合。在PAG中,发现表达sst2(a)受体的神经元共表达钙结合蛋白D28k(36%)、谷氨酸转运体EAAC-1(25%)和GABA转运体GAT-1(约10%)。总共65%的sst2(a)阳性神经元投射到丘脑。在脊髓中,sst2(a)受体显示与EAAC-1和GAT-1细胞共定位。在切断腰4和腰5背根后,使用[125I]BIM 23027进行免疫组织化学和受体放射自显影表明,初级传入神经元上不存在生长抑素sst2(a)受体。胸段脊髓背侧半切术并未改变生长抑素sst2(a)受体的免疫组织化学信号,为该受体蛋白在脊髓背角的内在定位提供了进一步证据。这些数据表明,生长抑素sst2(a)受体存在于形态学和神经化学上异质性的神经元上,并与参与镇痛和痛觉调制的脑区密切相关。