2.Hydrogen sulfide and nervous system regulation.
Cheng-Fang ZHOU ; Xiao-Qing TANG
Chinese Medical Journal 2011;124(21):3576-3582
OBJECTIVEThis review discusses the current status and progress in studies on the roles of hydrogen sulfide (H(2)S) in regulation of neurotoxicity, neuroprotection, and neuromodulator, as well as its therapeutic potential for neurodegenerative disorders.
DATA SOURCESThe data used in this review were mainly from Medline and PubMed published in English from 2001 to August 2011. The search terms were "hydrogen sulfide", "neuron", and "neurodegenerative disorders".
STUDY SELECTIONArticles regarding the regulation of neuronal function, the protection against neuronal damage and neurological diseases, and their possible cellular and molecular mechanisms associated with H(2)S were selected.
RESULTSThe inhibited generation of endogenous H(2)S is implicated in 1-methy-4-phenylpyridinium ion, 6-OHDA, and homocysteine-triggered neurotoxicity. H(2)S elicits neuroprotection in Alzheimer's disease and Parkinson's disease models as well as protecting neurons against oxidative stress, ischemia, and hypoxia-induced neuronal death. H(2)S offers anti-oxidant, anti-inflammatory and anti-apoptotic effects, as well as activates ATP-sensitive potassium channels and cystic fibrosis transmembrane conductance regulator Cl- channels. H(2)S regulates the long-term potentiation (LTP) and GABAB receptors in the hippocampus, as well as intracellular calcium and pH homeostasis in neurons and glia cells.
CONCLUSIONSThese articles suggest that endogenous H(2)S may regulate the toxicity of neurotoxin. H(2)S not only acts as a neuroprotectant but also serves as a novel neuromodulator.
Animals ; Humans ; Hydrogen Sulfide ; metabolism ; Nervous System ; metabolism ; Neuroprotective Agents ; metabolism ; Neurotoxins ; metabolism ; Neurotransmitter Agents ; metabolism
3.Epilepsy in various metabolic disorders.
Korean Journal of Pediatrics 2008;51(12):1290-1294
Seizures are a frequent symptom in metabolic disorders, although metabolic disorders are rarely found to be the cause of epilepsy. A precise diagnosis might not only influence treatment, but it might also call for counseling of the family, even if there are no direct therapeutic consequences. We review the main characteristics of epilepsy in metabolic disorders with regard to energy metabolism, toxic effects, neurotransmitters, and vitamins.
Counseling
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Energy Metabolism
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Epilepsy
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Humans
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Neurotransmitter Agents
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Seizures
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Vitamins
4.Progress in fluorescent visualization techniques for neurotransmitter detection.
Qiao HU ; Yuxin SHI ; Xiaoling YANG ; Jing ZHANG ; Bo LI ; Xiaoling LIAO ; Xue LIU
Chinese Journal of Biotechnology 2020;36(6):1051-1059
Neurotransmitters play an important role in nervous system. Temporal and spatial changes of neurotransmitter distribution are crucial to information processing in neural networks. Biosensors that can visually monitor neurotransmitters are one of the vital tools to explore a variety of physiological and pathological activities. This article reviews recent advances in monitoring neurotransmitters with high temporal and spatial resolution, and introduces the latest fluorescent imaging methods for typical neurotransmitters, including glutamate, dopamine, γ-aminobutyric acid and acetylcholine. The article also summarizes the basic principles, advantages and disadvantages of various visually detection methods, and provides systematic suggestions for designing neurotransmitter sensors with high temporal and spatial resolution.
Animals
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Biosensing Techniques
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instrumentation
;
trends
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Fluorescence
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Humans
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Neurotransmitter Agents
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metabolism
5.Therapy for hepatic encephalopathy.
Chinese Journal of Hepatology 2004;12(5):306-307
6.Detection of monoamine neurotransmitters and its metabolites by high performance liquid chromatograph after pre-column derivatization of dansyl chloride column.
Xiao HUANG ; Jia-wen CHEN ; Li-ping HE ; Xue-jun KANG
Chinese Journal of Preventive Medicine 2012;46(12):1117-1120
OBJECTIVETo develop a high performance liquid chromatography (HPLC) for detection of monoamine neurotransmitters and its metabolites after pre-column derivatization with dansyl chloride.
METHODSThe C(18) chromatograph column (150 mm×4.6 mm×5 µm) was selected for detection, and derived by dansyl chloride (10 mg/ml) under the condition of 50°C water bath by pH11 buffer solution. 20 µl acetic acid acetone solution (1.0 mol/L) was then mixed in for termination of the reaction. Then the solution was cooling to room temperature, 0.1 mol/L acetic acid zinc-acetonitrile-tetrahydrofuran solution was adopted for mobile phrase, with the volume ratio at 62:35:3. The flow rate was 1.0 ml/min between 0-10 min, 2.0 ml/min between 10-35 min. The ultraviolet detection wavelength was 286 nm. The above method separately detected monoamine neurotransmitters and its metabolites and evaluated the limit of detection, accurate degree and accuracy degree.
RESULTSThe linear relations between each component was good in the range of 1 - 20 µg/ml (r = 0.999). The lowest detection limit of norepinephrine, dopamine, 5-hydroxytryptamine and the metabolites 3-methoxy-4-benzoglycols, homovanillic acid and 5-heteroauxin were separately 0.60, 0.80, 0.41, 0.21, 0.19 and 0.1 µg/ml; while the average recovery rates were between 78.5% - 95.9%, and the relative standard deviation (RSD) was 6.62%, 7.64%, 2.98%, 3.60%, 5.09% and 3.09%, respectively. In the process of selection and optimization of the chromatographic conditions, we observed the importance of metal ions to discretion, and discussed the temperature, pH of the buffer solution and dosage of dansyl chloride in derivation. Under the above conditions, the reaction was perfect, and the baseline of the detected materials thoroughly separated.
CONCLUSIONThe method to detect monoamine neurotransmitters and its metabolites by HPLC and pre-column derivatization with dansyl chloride was established; and this method could provide reference for the detection of polyamine by HPLC.
Biogenic Monoamines ; analysis ; metabolism ; Chromatography, High Pressure Liquid ; methods ; Dansyl Compounds ; Neurotransmitter Agents ; analysis ; metabolism
7.Bone and Energy Metabolism.
Journal of Korean Diabetes 2013;14(4):174-177
Bone remodeling requires a large amount of energy, and is regulated by various hormones. Leptin, produced by adipocytes, is a well-known regulator of energy balance and is also involved in controlling bone mass through interaction with the central nervous system. Serotonin, downstream of leptin, is also emerging as a candidate for controlling energy balance and bone metabolism. Currently, bone is also considered to be an endocrine regulator of energy metabolism. Osteocalcin, secreted from osteoblasts, is known to be a key regulator of glucose and fat metabolism. In this review, we describe a novel concept that asserts that there exists a biological link between bone and energy metabolism, and we summarize what is currently known about the relationship between bone and energy metabolism.
Adipocytes
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Bone Remodeling
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Central Nervous System
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Energy Metabolism*
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Glucose
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Leptin
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Metabolism
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Neurotransmitter Agents
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Osteoblasts
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Osteocalcin
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Serotonin
8.Research progress--the role of astrocyte in neuronal functions.
Journal of Zhejiang University. Medical sciences 2008;37(5):531-536
Astrocytes can regulate synaptic transmission by releasing gliotransmitter, and also can promote synaptogenesis and neurogenesis by releasing estrogen, thrombospondins, IL-1beta and IL-6. Astrocytes may play critical roles in neural nutrition and neuroprotection, so that it might be a new target for treatment of certain central nervous system diseases.
Astrocytes
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physiology
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Estrogens
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metabolism
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Humans
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Interleukin-1beta
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metabolism
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Neurogenesis
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physiology
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Neurons
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physiology
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Neurotransmitter Agents
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metabolism
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Synaptic Transmission
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physiology
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Thrombospondins
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metabolism
9.Behavioral and neurobiological abnormalities induced by social isolation as a useful animal model of schizophrenia.
Ming LEI ; Lu LUO ; Shi-Qi MA ; Yan ZHANG ; Xi-Hong WU ; Liang LI
Acta Physiologica Sinica 2013;65(1):101-108
Social isolation influences the development of the brain, causing dysfunctions at behavioral, cellular and molecular levels. The present paper summarizes the abnormalities induced by social isolation in behaviors, neurotransmitters and cell apoptosis. At the behavioral level, social isolation induces hyperlocomotion, abnormalities in startle reflex and prepulse inhibition (PPI), and dysfunctions in conditioned learning, reversal learning and memory. Moreover, social isolation causes changes of neurotransmitters, such as the increase of dopamine in the nucleus accumbens, the amygdala and other brain regions in the limbic system, the decrease of dopamine in medial prefrontal cortex, the decrease of 5-HT in the nucleus accumbens and the hippocampus, and changes of glutamine in the prefrontal cortex. Finally, social isolation affects cell apoptosis in different brain areas, such as the medial prefrontal cortex, amygdala, nucleus accumbens, and hippocampus. Both the changes in neurotransmitters and cell apoptosis may contribute to the behavioral dysfunctions in social isolated rats. Since schizophrenic patients have similar abnormalities in behaviors and neurotransmitters, isolation rearing can be used as a useful animal model of schizophrenia.
Animals
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Brain
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physiopathology
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Disease Models, Animal
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Neurotransmitter Agents
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metabolism
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Rats
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Schizophrenia
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physiopathology
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Social Isolation
10.Mechanisms of postoperative pain.
Chinese Medical Journal 2007;120(22):1949-1950