1.Change of GABA immunoreactivity in area tempestas of epileptic sensitive rats.
Xin-Lu DU ; Jie ZHAO ; Wan-Qin ZHANG
Chinese Journal of Applied Physiology 2002;18(2):207-208
Animals
;
Epilepsy
;
immunology
;
metabolism
;
Hippocampus
;
metabolism
;
Male
;
Rats
;
Rats, Sprague-Dawley
;
gamma-Aminobutyric Acid
;
immunology
;
metabolism
2.Effect of propofol at uptake equilibrium on γ-aminobutyric acid in different cerebral regions in dogs.
Yan WANG ; Chun-Shui LIN ; Miao-Ning GU ; Gao-Feng GUO ; Zhi-Feng ZHOU ; Ying CHEN
Journal of Southern Medical University 2012;32(3):427-429
OBJECTIVETo investigate the effect of propofol at doses for different anesthesia depths on γ-aminobutyric acid (GABA) in different cerebral regions at propofol uptake equilibrium in dogs.
METHODSTwelve 12-18-month-old healthy hybrid dogs weighing 10-12 kg were randomly divided into light anesthesia group (n=6) and deep anesthesia group (n=6) with a single bolus dose of propofol (5.5 and 7.0 mg/kg, respectively) completed in 15 s followed by intravenous propofol infusion at a constant rate (55 and 70 mg·kg(-1)·h(-1), respectively). Blood samples (2 ml) were taken from the internal carotid artery and jugular vein to measure plasma propofol concentrations 50 min after the start of the infusion. The dogs were then sacrificed and tissues were taken from different brain regions and the cervical cord to measure GABA concentrations using high-pressure liquid chromatography (HPLC).
RESULTSThe plasma propofol concentrations in internal carotid artery and jugular vein were similar in both light anesthesia group (3.00 ± 0.31 and 3.10 ± 0.51 µg/ml, respectively, P>0.05) and deep anesthesia group (6.41 ± 0.05 and 6.40 ± 0.11 µg/ml, respectively, P>0.05). GABA concentrations in the brain regions were significantly higher in deep anesthesia group than in light anesthesia group (P<0.05). The dorsal thalamus and hypothalamus showed greater GABA variations [(83.83 ± 2.230%) and (85.83 ± 1.72)%] compared to other brain regions at different anesthesia depths (P<0.05).
CONCLUSIONSIn both groups, plasma propofol concentrations in the internal carotid artery and internal jugular vein reach equilibrium at 50 min of propofol infusion. The variation of GABA is associated with the anesthesia depth of propofol, and GABA variation in the dorsal thalamus and hypothalamus plays an important role in propofol anesthesia.
Anesthetics, Intravenous ; pharmacokinetics ; Animals ; Brain ; metabolism ; Dogs ; Female ; Male ; Propofol ; blood ; pharmacokinetics ; gamma-Aminobutyric Acid ; metabolism
3.Effect of gamma-aminobutyric acid on the sperm acrosin activity.
Shu-Ling BIAN ; Wei ZHANG ; Hui ZHU ; Jiang NI ; Lan-Chun YAO ; Liang CHEN
National Journal of Andrology 2002;8(5):326-328
OBJECTIVESTo investigate the effect of gamma-aminobutyric acid (GABA) on the sperm acrosin activity in normal men and positive antisperm antibody (AsAb) men.
METHODSSperm acrosin activity was detected by BAEE/ADH method.
RESULTSGABA could increase the sperm acrosin activity in normal and AsAb positive patients (P < 0.01). The results also indicated that GABA significantly increased Na(+)-K(+)-ATPase activity (P < 0.01), Ca(2+)-ATPase activity (P < 0.05) and SOD activity (P < 0.01) of sperm.
CONCLUSIONSThe results demonstrated that GABA could influence the sperm acrosin activity.
Acrosin ; metabolism ; Humans ; Male ; Spermatozoa ; drug effects ; immunology ; metabolism ; gamma-Aminobutyric Acid ; pharmacology
4.Pathogenesis of hepatic encephalopathy.
Chinese Journal of Hepatology 2004;12(5):304-304
5.Effect of thiopental sodium on the release of glutamate and gamma-aminobutyric acid from rats prefrontal cortical synaptosomes.
Hongliang, LIU ; Shanglong, YAO
Journal of Huazhong University of Science and Technology (Medical Sciences) 2004;24(6):602-4
To investigate the effect of thiopental sodium on the release of glutamate and gamma-aminobutyric acid (GABA) from synaptosomes in the prefrontal cortex, synaptosomes were made, the spontaneous release and the evoked release by 30 mmol/L KCl or 20 micromol/L veratridine of glutamate and GABA were performed under various concentrations of thiopental sodium (10-300 micromol/L), glutamate and GABA concentrations were determined by reversed-phase high-performance liquid chromatography. Our results showed that spontaneous release and evoked release of glutamate were significantly inhibited by 30 micromol/L, 100 micromol/L and 300 micromol/L thiopental sodium, IC50 of thiopental sodium was 25.8 +/- 2.3 micromol/L for the spontaneous release, 23.4 +/- 2.4 micromol/L for KCl-evoked release, and 24.3 +/- 1.8 micromol/L for veratridine-evoked release. But GABA spontaneous release and evoked release were unaffected. The study showed that thiopental sodium with clinically related concentrations could inhibit the release of glutamate, but had no effect on the release of GABA from rats prefrontal cortical synaptosomes.
Glutamic Acid/*metabolism
;
Hypnotics and Sedatives/pharmacology
;
Prefrontal Cortex/*metabolism
;
Rats, Sprague-Dawley
;
Synaptosomes/*metabolism
;
Thiopental/*pharmacology
;
gamma-Aminobutyric Acid/*metabolism
6.The changes of GABA and GABAergic neurons in inferior colliculus of unilateral cochlear damage rats.
Qinying WANG ; Qingquan HUA ; Shenqing WANG ; Bokui XIAO ; Hua LIAO
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2007;21(7):321-323
OBJECTIVE:
To observe the changes of GABA and GABAergic neurons in rat inferior colliculus following unilateral cochlear damage and explore the function and significance of GABA in reorganization of auditory center after deafferentation.
METHOD:
Twenty sprague dawley rats were divided into four groups randomly. The technique of direct anti-GABA immunocytochemistry (SP) was used in this study. The quantity of GABA was measured by 835-50 type Amino Acid Automatism Analyzer and compared at one week, two weeks and one month after unilateral cochlear ablation, respectively.
RESULT:
Compared with controlled groups, the quantity levels of GABA decreased and the number of GABAergic neurons also reduced one week after unilateral cochlear damage and there was a significant difference in GABA between two groups( P <0. 05); after one month, the quantity of GABA and the number of GABAergic neurons almost reached the normal level, the differences were no significant.
CONCLUSION
The dynamic change of GABA in rat inferior colliculus reflected the neuronal activity, which implied that GABA may play an important role in reorganization of auditory center after unilateral cochlear damage.
Animals
;
Cochlea
;
metabolism
;
pathology
;
Inferior Colliculi
;
metabolism
;
Neurons
;
metabolism
;
Rats
;
Rats, Sprague-Dawley
;
gamma-Aminobutyric Acid
;
metabolism
8.Progress in studies on the role of gamma-aminobutyric acid.
Chinese Medical Journal 2012;125(7):1322-1330
9.Effects of pyrethroids on the activity of gamma-aminobutyric acid transferase in rat brain.
Zhi-ying JI ; Nian SHI ; Su-qing WANG ; Jie DONG ; Mao-shan CHEN
Chinese Journal of Industrial Hygiene and Occupational Diseases 2003;21(3):197-199
OBJECTIVETo study the effects of pyrethroids on the activity of gamma-aminobutyric acid transferase (GABAT) in rat brain.
METHODThe coupled enzyme ultraviolet spectrophotography was applied to observe the effects of deltamethrin (DM) and permethrin (PM) on the activities of GABAT in rat cerebral cortex, hippocampus, corpus striatum and cerebellum in vitro and in vivo.
RESULTSIn vitro, DM and PM had no significant effects on the activities of GABAT in rat cerebral cortex, hippocampus, corpus striatum and cerebellum at the final concentration of 10(-9) - 10(-4) mol/L. When 37.5 mg/kg DM and 600 mg/kg PM were orally administrated to the rats at one time, the activities of GABAT in rat cerebral cortex, hippocampus and cerebellum in the DM group [(2.96 +/- 0.43), (2.13 +/-0.44), (5.12 +/- 1.36) nmol x mg pro(-1) x min(-1), respectively] were lower than those in the control group [(3.43 +/- 0.41), (2.68 +/- 0.47), (6.74 +/- 1.64) nmol x mg pro(-1) x min(-1)] (P < 0.05), and the activities of GABAT in rat cerebral cortex and hippocampus in the PM group [(4.57 +/- 0.30), (4.18 +/- 0.63) nmol.mg pro(-1) x min(-1), respectively] were higher than those in the control group (P < 0.05). When 12.5 mg/kg DM and 200 mg/kg PM were orally administrated to the rats once a day for consecutive five days, the two pesticides had no significant effects on the activities of GABAT in rat cerebral cortex, hippocampus, corpus striatum and cerebellum (P > 0.05).
CONCLUSIONSIn vitro, DM and PM had no significant effects on the activity of GABAT in rat brain; in vivo, DM and PM may have different effects on the activity of GABAT in rat brain, which deserve further study.
Animals ; Brain ; drug effects ; enzymology ; In Vitro Techniques ; Insecticides ; toxicity ; Male ; Pyrethrins ; toxicity ; Rats ; Spectrophotometry ; Transferases ; metabolism ; gamma-Aminobutyric Acid ; metabolism
10.Screening and identification of GABA-producing microbes in fermentation process of Sojae Semen Praeparatum.
Jing-Jing XIONG ; Jia-Xiu REN ; Shu-Han ZHOU ; Ming-Sheng SU ; Li-Yuan WANG ; Mei-Zhi WENG ; Wei-Hua XIE ; Xiao-Mei XIE
China Journal of Chinese Materia Medica 2019;44(11):2266-2273
A high-content GABA was found in Sojae Semen Praeparatum(SSP), which is a famous traditional Chinese medicine and officially listed in Chinese Pharmacopoeia. To screen out and identify GABA-producing microbes from samples at different time points during the fermenting process of SSP, traditional microbiological methods combined with molecular biological methods were used to study the predominant GABA-producing microorganisms existing in the fermenting process of SSP. This study would lay a foundation for further studying the processing mechanism of SSP. The fermenting process of SSP was based on Chinese Pharmacopoeia(2010 edition), and samples were taken at different time points during the fermenting process of SSP. The bacteria and fungi from samples at different time points in the fermenting process of SSP were cultured, isolated and purified by selective medium, and dominant strains were selected. The dominant bacteria were cultured in the designated liquid medium to prepare the fermentation broths, and GABA in the fermentation broth was qualitatively screened out by thin-layer chromatography. The microbial fermentation broth with GABA spots in the primary screening was quantitatively detected by online pre-column derivatization and high performance liquid chromatography established in our laboratory. GABA-producing microorganisms were screened out from predominant strains, and their GABA contents in fermentation broth were determined. The DNA sequences of GABA-producing bacteria and fungi were amplified using 16S rDNA and 18S rDNA sequences by PCR respectively. The amplified products were sequenced, and the sequencing results were identified through NCBI homology comparison. Molecular biological identification was made by phylogenetic tree constructed by MEGA 7.0 software. Through the homology comparison of NCBI and the construction of phylogenetic tree by MEGA 7.0 software, nine GABA-producing microorganisms were screened out and identified in this study. They were Bacillus subtilis, Enterococcus faecium, E. avium, Aspergillus tamarii, A. flavus, A. niger, Cladosporium tenuissimum, Penicillium citrinum and Phanerochaete sordida respectively. For the first time, nine GABA-producing microorganisms were screened out and identified in the samples at different time points during the fermenting process of SSP in this study. The results indicated that multiple predominant GABA-producing microorganisms exist in the fermenting process of SSP and may play an important role in the formation of GABA.
Bacteria
;
classification
;
metabolism
;
Chromatography, High Pressure Liquid
;
Fermentation
;
Fungi
;
classification
;
metabolism
;
Phylogeny
;
Seeds
;
microbiology
;
Soybeans
;
microbiology
;
gamma-Aminobutyric Acid
;
biosynthesis