EFFECT OF INJEClTION OF THYROTROPIN—RELEASING HORMONE INTO NUCLEUS ACCUMBENS ON THE PAIN DISCH—ARGES IN NUCLEUS PARAFASCI—CULARIS OF RAT-THALAMUS
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EFFECT OF INJEClTION OF THYROTROPIN—RELEASING HORMONE INTO NUCLEUS ACCUMBENS ON THE PAIN DISCH—ARGES IN NUCLEUS PARAFASCI—CULARIS OF RAT-THALAMUS
Acupuncture ResearchIssue 3, Pages: 222-226(1990)
作者机构:
同济医科大学生理教研室
作者简介:
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Published:1990
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Nie zhiguo, Liu zuoyan. EFFECT OF INJEClTION OF THYROTROPIN—RELEASING HORMONE INTO NUCLEUS ACCUMBENS ON THE PAIN DISCH—ARGES IN NUCLEUS PARAFASCI—CULARIS OF RAT-THALAMUS[J]. Acupuncture research, 1990, (3): 222-226.
DOI:
Nie zhiguo, Liu zuoyan. EFFECT OF INJEClTION OF THYROTROPIN—RELEASING HORMONE INTO NUCLEUS ACCUMBENS ON THE PAIN DISCH—ARGES IN NUCLEUS PARAFASCI—CULARIS OF RAT-THALAMUS[J]. Acupuncture research, 1990, (3): 222-226.DOI:
EFFECT OF INJEClTION OF THYROTROPIN—RELEASING HORMONE INTO NUCLEUS ACCUMBENS ON THE PAIN DISCH—ARGES IN NUCLEUS PARAFASCI—CULARIS OF RAT-THALAMUS
摘要
近年来大量实验表明
广泛分布于中枢神经系统的促甲状腺素释放激素(TRH)参与多种生理功能的调节。脑室微量注射TRH
可提高小鼠的痛阈
提示TRH可能参与中枢镇痛过程、伏核、杏仁核及尾核是针刺镇痛和痛觉调制中的重要结构。免疫Glass microelectaod recording method was used to investigate the effect of thyrotropin-releasing hormone(TRH) into nucleus accumbens
nucleus amygdaloid or nucleus caudate-putamen on unit discharges of pain-excitation neurons (PEN) in nucleus parafascicularis of thalamus in rats. The results showed that: (1) TRH injccted into the nucleus accumbens results in a significant ihhibition of pa- in discharges of PEN in nucleus parafascicularis. But injection of TRH into nuc- leus amygdaloid
nucleus caudate-putamen had no significant effect. (2) Pretreat- ment with auropine abolished the inhibitory effect of TRH. (3)'Pretaeatment with haloperidol also adolished the inhibitory effect of TRH. (4) Pretaeatment with naloxone
propranolol or phen-tolamine did not affect the inhibitory effect of TRH. The results mentioned above suggested that nucleus accumbens could be a sp- ecial area in response to TRH and the effect of TRH seems to be involved in both cholinergic M-receptor and dopamine receptor.