The monoaminergic modulation of spinal motor function and the alteration in the motor disease
The monoaminergic modulation of spinal motor function and the alteration in the motor disease
批准号:
15590134
负责人:
ONO Hideki
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004
中文摘要
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英文摘要
The descending noradrenergic and serotonergic systems modulate the function of the spinal α-motoneurons which control movements of body and limbs. However, the function and changes in neuronal disease are unclear. In the present study, the following results were obtained.1. Serotonergic agonists have been shown both to increase and decrease spinal motor transmission. Motoneurons possess somatodendritic serotonin (5-HT)_2 receptors, which account for the increased excitability. However, it is unclear which receptor subtypes mediate the inhibitory effects on spinal reflexes. We showed that 5-HT_<1B> and 5-HT_<1D> receptors located in the spinal cord mediate the 5-HT-induced inhibition of spinal reflexes.2. Spinal reflexes and recurrent and presynaptic inhibitions in streptozotocin (STZ)-induced diabetic rats were examined. The recurrent inhibition which is mediated by glycine was depressed in diabetic rats. In addition, the inhibitory effect of 5-HT was decreased in those rats. These res … More ults show that the diabetogenic degeneration occurred in not only sensory but also motor systems.3. The relationships between ataxia and the monoamines concentrations of central nervous systems were examined in spinocerebellar atrophy (SCD) model mice. Two SCD model mice, rolling mouse Nagoya (RMN) and Ara-C mice which were produced by the administration of cytosine arabinoside on 2, 3, 4 days after birth, were used. The concentrations of monoamines were increased in CNS of these SCD model mice. The repeated administration of taltirelin hydrate, which is clinically used for SCD treatment, improved ataxia, but did not affect the monoamines concentration of CNS in RMN and Ara-C mice.4. We showed that the noxious stimuli-evoked flexor reflex of mice were composed from Aδ-fiber mediated short-latency and C-fiber-mediated long-latency withdrawal movements. These withdrawal movements are facilitated by repeated stimulation, it is called wind-up. In STZ-induced diabetic mice, the wind-up of C-fiber-mediated movement, but not Aδ-fiber-mediated one, was enhanced significantly. Less
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Kimura, S., Honda, M., Tanabe, M., Ono, H.: "Noxious stimuli evoke a biphasic flexor reflex composed of AS-fiber-mediated short-latency and C-fiber-mediated long latency withdrowal movements in mice"J.of Pharmacological Sciences. (2004)
Kimura, S.、Honda, M.、Tanabe, M.、Ono, H.:“有害刺激会引起小鼠双相屈肌反射,由 AS 纤维介导的短潜伏期和 C 纤维介导的长潜伏期缩回运动组成
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Endogenously released 5-hydroxytryptamine depress the spinal mono-synaptic reflex via 5-HT_<1D> receptors
内源性释放的 5-羟色胺通过 5-HT_<1D> 受体抑制脊髓单突触反射
DOI:
--
发表时间:
2004
期刊:
Eur.J.Pharmacology 503
影响因子:
--
作者:
[Honda, M. et al.]
通讯作者:
M. et al.
Honda, M., Tanabe, M., Ono H.: "Serotonergic depression of spinal monosynaptic transmission is mediated by 5-HT_<1B> receptors"Eur.J.Pharmacology. 482. 155-161 (2003)
Honda,M.,Tanabe,M.,Ono H.:“脊髓单突触传递的血清素能抑制是由5-HT_ 1B 受体介导的”Eur.J.Pharmacology。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Endogenously released 5-hydroxytryptamine depress the spinal monosynaptic reflex via 5-HT_<1D> receptors
内源性释放的 5-羟色胺通过 5-HT_<1D> 受体抑制脊髓单突触反射
DOI:
--
发表时间:
2004
期刊:
Eur. J. Pharmacol. 503
影响因子:
--
作者:
[Kimura, S. et al., S.Kimura et al., M.Honda et al.]
通讯作者:
M.Honda et al.
DOI:
10.1254/jphs.fp0040785
发表时间:
2005-02-01
期刊:
JOURNAL OF PHARMACOLOGICAL SCIENCES
影响因子:
3.5
作者:
[Kimura, S, Tanabe, M, Ono, H]
通讯作者:
Ono, H
共 8 条
Spinal Cord Injury : Establishment of Measurement for Electrophysiological Function and Pharmacological Evaluation of Drugs
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批准号:20590086
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.08万
-
财政年份:2008
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负责人:ONO Hideki
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依托单位:
Role of imidazoline receptors in modulation of muscle tone and pain
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批准号:12672124
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.11万
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财政年份:2000
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负责人:ONO Hideki
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依托单位:
下行性の筋緊張制御における脊髄のセロトニン1Aおよび2受容体の役割
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批准号:09672258
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:1997
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负责人:ONO Hideki
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依托单位:
The Study of TRH-containing Nervous Systems in the Spinal Cord
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批准号:60571035
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$0.26万
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财政年份:1985
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负责人:ONO Hideki
-
依托单位:
海外基金