• Title/Summary/Keyword: Somatostatin 신경세포

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IMMUNOHISTOCHEMICAL STUDY ON THE POSTNATAL DEVELOPMENT OF SOMATOSTATIN IMMUNOREACTIVE NEURONS IN THE RAT CEREBRAL CORTEX (흰쥐 대뇌피질에서의 Somatostatin 신경세포의 생후발달에 관한 면역조직화학적 연구)

  • Kim, Seon-Mi;Cha, Choong-Ik;Hong, Kang-E
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • v.4 no.1
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    • pp.79-90
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    • 1993
  • With immunohistochemical method, We have examined the distribution, the size, the number, and the morphology of somatostatin-immunoreactive neurons in the cerebral cortex of rats at the 1st. 2nd, 3rd, 4th postnatal week and the 2nd and 3rd months of age. The results are summarized as follows : 1) Strongly immunoreactive somatostatin neurons were found in the layer V and VI at the first postnatal week and then they were observed to be densely populated in the layer II and III from the 3rd postnatal week on as in the adult rat. 2) The size of the neuron was largest at the 2nd postnatal week while the number of the neurons was greatest in the 1st or 2nd postnatal week, depending on the different areas of the cortex. Overall the postnatal development of somatostatin neurons are well corresponds with the general principle of neuronal development of CNS.

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Immuno-Electron Microscopic Studies on the Localization of Serotonin and Somatostatin in the Optic Lobes of Cephalopods (Todarodes pacificus and Octopus minor) Inhabiting the Korean Waters (한국 연근해산 두족류 (Todarodes pacificus and Octopus minor) 시엽 (Optic lobe)내 Serotonin 및 Somatostatin의 분포에 관한 면역전자현미경적 연구)

  • Chang, Nam-Sub;Han, Jong-Min;Kim, Sang-Won;Lee, Kwang-Ju;Hwang, Sun-Jong;Lee, Jung-Chan
    • Applied Microscopy
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    • v.32 no.3
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    • pp.247-255
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    • 2002
  • In this study, we carried out immunostaining and immunogold labeling with antibodies to serotonin and somatostatin to examine the characteristics and functions of the neurons that secrete neurotransmitters in optic lobes of Todarodes pacificus and Octopus minor. As a result of immunostaining with anti-somatostatin, the nerve cells of Todarodes pacificus reacted as similar to the anti-serotonin, but in Octopus minor, only large cells in the outer granule cell layer reacted positively. In the immunogold labeling with anti-serotonin, the nerve cells in the inner grande cell layer and medulla of Todarodes pacificus reacted strongly, 30 gold particles being labeled per $0.5{\mu}m^2$ of the cytoplasm. However, in Octopus minor, only 17 gold particles were labeled, which stated a weak reaction. On the other hand, in the anti-somatostatin case, the nerve cells in the outer and inner granule cell layers and medulla of Todarodes pacificus showed strong reaction, 30 gold particles being labeled per $0.5{\mu}m^2$ of the cytoplasm while the nerve cells in the outer granule cell layer of Octopus minor reacted weakly, about 3 gold particles being labeled per the equivalent area. As a result of immunostaining and immunogold labeling with two types of antibodies to each part of the optic lobes, we found that the reactive nerve cells were distributed differently in the two species. In particular, the degree of reactivity to the immunostaining and immunogold labeling appeared stronger in Todarodes pacificus than in Octopus minor.

Immunohistochemical Studies on the Visceral Ganglion and Right Parietal Ganglion of the African Giant Snail, Achatina fulica (아프리카왕달팽이(Achatina fulica) 내장신경절 및 우체벽신경절에 관한 연구 I. 면역조직화학적 방법)

  • 장남섭;김상원;한종민;이광주;황선종
    • The Korean Journal of Malacology
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    • v.16 no.1_2
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    • pp.1-9
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    • 2000
  • The visceral ganglion and the right parietal ganglion of the African giant snail, Achatina fulica, consists of two hemispheres, each in left and right side, respectively, like a butterfly. The surface of cortex and medulla in the two ganglions are crowded with nerve cells, but nerve fibers form a network at the middle portion. The nerve cells in the cortex and medulla of the visceral ganglion and the right parietal ganglion are classified into the following four classes according to their sizes: giant (above 200 ${\mu}{\textrm}{m}$, in diameter), large (60-70 ${\mu}{\textrm}{m}$, in diameter), middle (30-40 ${\mu}{\textrm}{m}$, in diameter) and small (10-15 ${\mu}{\textrm}{m}$, in diameter) nerve cells, respectively. The giant and large nerve cells are rarely found(20-22 eas. in total) while the middle and small nerve cells are found in large quantities (middle: 400-500 eas., small: 700-800 eas.). In the AB/AY double staining, the giant nerve cell is identified as light yellow cells (LYC), while large and middle none cells as dark green cells (DGC) or yellow green cells (YGC), and small nerve cells as yellow cells (YC) or blue cells (BC), The DGC, which reacts positively to somatostatin immunostain reaction, inhibits the secretion of the growth control hormone. The giant and large nerve cells are identified to do the functions of phagocytosis as well as neurosecretion.

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Distribution of growth hormone-releasing factor- and somatostatin-immunoreactive neurons in the hypothalamus of the Korean squirrel(sciurus vulgalis coreae) (청서 시상하부의 growth hormone-releasing factor 및 somatostatin 면역반응신경세포의 분포)

  • Jeong, Young-gil;Son, Hwa-young;Yoon, Won-kee;Kim, Kil-soo;Won, Moo-ho;Ryu, Si-yun;Cho, Sung-whan;Kim, Moo-kang
    • Korean Journal of Veterinary Research
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    • v.35 no.4
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    • pp.671-681
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    • 1995
  • This study was attempted to investigate the topographical distribution, shape and immunoreactivity of growth hormone-releasing factor(GRF)- and somatostatin(SOM)-immunoreactive neurons in the hypothalamus of the Korean squirrels(Sciurus vulgalis coreae). For the light microscopical examination of immunohistochemistry, the brains were fixed with 4% paraformaldehyde solution by means of intracardiac perfusion. And the frozen sections($40{\mu}m$ thick) were stained immunohistochemically by ABC method. Distribution of GRF immunoreactive neurons($12-17{\mu}m$) was highest in the paraventricular nucleus, moderate in the periventricular and supraoptic nuclei, and low in the arcuate nucleus and lateral hypothalamic area. Their immunoreactive fibers were found very high in the median eminence, moderately in the supraoptic, paraventricular and periventricular nuclei, and low in the arcuate nucleus and lateral hypothalamic area. SOM immunoreactive perikarya($14-18{\mu}m$) were found moderately in the periventricular nucleus near the subependymal layer of the third ventricle, and low in the arcuate and suprachiasmatic nuclei. SOM immunoreactive fibers were found high in the median eminence, and moderately or low in the arcuate and periventricular nuclei.

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Effect of Cholecystokinin on Serotonin Release from Cultured Neurons of Fetal Rat Medulla Oblongata (연수 신경세포 배양에서 세로토닌 분비에 대한 Cholecystokinin의 작용)

  • Song Dong-Keun;Cho Hyun-Mi;Lee Tae-Hee;Suh Hong-Won;Kim Yung-Hi
    • The Korean Journal of Pharmacology
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    • v.31 no.1 s.57
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    • pp.11-15
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    • 1995
  • Serotonergic neurons in medulla oblongata play an important role in the endogenous descending pain inhibitory system. To illucidate the factors involved in the regulation of medullary serotonergic neurons, we studied the effects of cholecystokinin (CCK) and agents acting on various second messenger systems on 5-hydroxytryptamine (5-HT) release from cultured neurons of rat fetal (gestational age 14th day) medulla oblongata. Cultured cells maintained for 10 days in vitro were stimulated for 48 hours with CCK or other neuropeptides at 10 micromolar concentration. CCK ($10{\mu}M$) and substance P ($10{\mu}M$) significantly increased. 5-HT release. However, somatostatin, proctolin, thyrotropin releasing hormone, and interleukin-6 did not have any effects on 5-HT release. Nimodipine ($1{\mu}M$), a calcium channel blocker, almost completely, and calmidazolium ($1{\mu}M$), a calmodulin antagonist, significantly inhibited the CCK-induced 5-HT release. The total 5-HT content (intracellular 5-HT plus released 5-HT) was significantly increased by CCK. However, the intracellular 5-HT content was not significantly changed by CCK. Forskolin ($5{\mu}M$), an adenylate cyclase activiator, but not $2{\mu}M$ phorbol myristate acetate (PMA), a protein kinase C activator, significantly enhanced 5-HT release. The total 5-HT content (intracellular 5-HT plus released 5-HT) was significantly increased by forskolin. However, the intracellular 5-HT content was not significantly changed by forskolin. PMA had no effect on intracellular 5-HT levels. These results suggest that CCK regulates serotonergic neurons in the medulla oblongata by enhancing 5-HT secretion through calcium influx and caimodulin, and that cyclic AMP system but not protein kinase C system is involved in 5-HT release.

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