scholarly journals Inter- and intracellular relationship of substance P-containing neurons with serotonin and GABA in the dorsal raphe nucleus: combination of autoradiographic and immunocytochemical techniques.

1986 ◽  
Vol 34 (6) ◽  
pp. 735-742 ◽  
Author(s):  
R Mâgoul ◽  
B Onteniente ◽  
A Oblin ◽  
A Calas

Double-labeling experiments were performed at the electron microscopic level in the dorsal raphe nucleus of rat, in order to study the inter- and intracellular relationship of substance P with gamma-aminobutyric acid (GABA) and serotonin. Autoradiography for either [3H]serotonin or [3H]GABA was coupled, on the same tissue section, with peroxidase-antiperoxidase immunocytochemistry for substance P in colchicine-treated animals. Intercellular relationships were represented by synaptic contacts made by [3H]serotonin-labeled terminals on substance P-containing somata and dendrites, and by substance P-containing terminals on [3H]GABA-labeled cells. Intracellular relationships were suggested by the occurrence of the peptide within [3H]serotonin-containing and [3H]GABA-containing cell bodies and fibers. Doubly labeled varicosities of the two kinds were also observed in the supraependymal plexus adjacent to the dorsal raphe nucleus. The results demonstrated that, in addition to reciprocal synaptic interactions made by substance P with serotonin and GABA, the dorsal raphe nucleus is the site of intracellular relationships between the peptide and either the amine or the amino acid.

1989 ◽  
Vol 62 (2) ◽  
pp. 481-486 ◽  
Author(s):  
Z. Z. Pan ◽  
W. F. Colmers ◽  
J. T. Williams

1. Intracellular recordings from neurons within dorsal raphe nucleus in slices from rat brain were used to study an inhibitory postsynaptic potential (IPSP) evoked by electrical stimulation. 2. The IPSP was observed in approximately 70% of neurons, had a latency to onset of 40-65 ms, reached a peak in 350-400 ms, had a total duration of 1-2 s, and reversed polarity at the potassium equilibrium potential. 3. This IPSP was blocked by spiperone (1 microM) and prolonged by fluoxetine (300 nM-30 microM) suggesting that it was mediated by 5-hydroxytryptamine (5-HT). 4. Superfusion with gamma-aminobutyric acid (GABA) and excitatory amino acid receptor antagonists were used to block "fast" synaptic potentials that preceded the IPSP such that it could be studied in isolation. Blockade of the GABA-mediated synaptic potentials increased the amplitude of the IPSP by 1.3-fold. The amplitude of the IPSP was reduced by 30% after blockade of the excitatory amino acid-mediated synaptic potential. 5. The results indicate that the IPSP recorded in dorsal raphe neurons was caused by 5-HT released at least in part from indirect (synaptically induced) excitation of 5-HT-containing cells within the slice.


2009 ◽  
Vol 29 (12) ◽  
pp. 2303-2314 ◽  
Author(s):  
Baptiste Lacoste ◽  
Mustapha Riad ◽  
Marc-Olivier Ratté ◽  
Sandra M. Boye ◽  
Daniel Lévesque ◽  
...  

Neuroscience ◽  
1991 ◽  
Vol 42 (3) ◽  
pp. 757-775 ◽  
Author(s):  
K.G. Baker ◽  
G.M. Halliday ◽  
J.-P. Hornung ◽  
L.B. Geffen ◽  
R.G.H. Cotton ◽  
...  

2021 ◽  
Author(s):  
Xiaoju LIU ◽  
Hai-juan Wang ◽  
Jie Gao ◽  
Xiao-yu Wang ◽  
Yin-xia Ning

Abstract Background: To explore the intervention mechanism of Baixiangdan Capsule(BXD) and Shuyu Capsule(SY) in the treatment of anger-out and anger-in. A kind of GABABR1(GB1) mediated GABA in the dorsal raphe nucleus(DRN) regulating serotonin(5-HT) levels in the Prefrontal Cortex(PFC), Hippocampus and Hypothalamus in Anger-out and Anger-in male rats. To further explore the difference of Baixiangdan Capsule(BXD) and Shuyu Capsule(SY) in the treatment of anger-out and anger-in.Methods: The anger rat model was established by social isolation combined with resident-intruder paradigm, and behavioral evaluation was used to screen and distinguish anger-out and anger-in model rats. BXD and SY were intervention drugs of anger–out and anger-in rats respectively. On this basis, ELISA was used to detect GABA content in DRN and 5-HT contents in PFC, hippocampus and hypothalamus after different time course (0,1,3,5,7 days) treated with BXD and SY. The co expression of 5-HT and GB1 in DRN was detected by immunofluorescence double labeling technique. Finally, brain stereotactic localization was performed after baclofen, the GB1 specific agonist, and CGP35348, the GB1 specific inhibitor, were injected into the DRN, the 5-HT contents in PFC, hippocampus and hypothalamus was detected by ELISA.Results: After drug treatment, ABT scores and OFT total distance in BXD group were significantly decreased to the level of control group (P<0.05). On the contrary, that in SY group were significantly increased to the level of control group (P<0.05). The sugar water preference coefficient of BXD group and SY group was significantly increased to the normal level (P<0.05). With the increase of the medication duration, 5-HT levels in PFC, hypothalamus and hippocampus increased, gradually corrected its abnormal decline, and returned to the normal level on the 7th day. Besides, GABA level in DRN decreased, gradually corrected its abnormal increase, and also returned to normal level on the 7th day. A large number of 5-HT positive cells (red) in DRN could be seen on immunofluorescence section, and GB1 positive cells (green) could also be seen. Besides, after the drug intervention, 5-HT level in DRN was elevated to normal level (P<0.05). GB1 level in DRN was decreased to normal level in BXD group and SY group (P<0.05). Compared with saline injection, 5-HT levels in PFC, hypothalamus and hippocampus in each group was significantly decreased after injection of baclofen into the DRN (P < 0.05). On the contrary, 5-HT levels in PFC, hypothalamus and hippocampus in each group was significantly increased after the injection of CGP35348 into the DRN.Conclusions: BXD and SY can effectively improve the abnormal behavior changes of anger-out and anger-in rats, and the optimal duration of action is 7 days. The improvement way is to correct the following abnormal changes: The significantly increased GABA in DRN combined with a significantly increased GB1 on 5-HT neurons in DRN, which further mediated the synaptic inhibition effect, thereby reducing 5-HT level of 5-HT neurons in DRN, resulting in a significant decrease of 5-HT levels in PFC, hypothalamus and hippocampus. Therefore, GB1 mediated GABA in DRN can regulate 5-HT levels in PFC, hypothalamus and hippocampus, which may be one of the ways that BXD and SY treat anger-out and anger-in.


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