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必需脂肪酸调节阿扑吗啡在猫尾状核切片中多巴胺受体上的活性。

Essential fatty acids modulate apomorphine activity at dopamine receptors in cat caudate slices.

作者信息

Davidson B, Kurstjens N P, Patton J, Cantrill R C

机构信息

Department of Medical Biochemistry, University of the Witwatersrand Medical School, Johannesburg, South Africa.

出版信息

Eur J Pharmacol. 1988 May 10;149(3):317-22. doi: 10.1016/0014-2999(88)90662-0.

DOI:10.1016/0014-2999(88)90662-0
PMID:2900769
Abstract

We have used a classical neurotransmitter release model to investigate the effect of dietary polyenoic fatty acids on the sensitivity of the presynaptic dopamine autoreceptor in slices of cat caudate nucleus. Maximum inhibition of [3H]dopamine release was seen only in animals fed a diet containing post delta-6-desaturation fatty acids of both the w3 and w6 series. The removal of either or both groups of fatty acids resulted in attenuation of sensitivity of the autoreceptor to apomorphine. We propose that a balance of w3 and w6 fatty acids is required to maintain normal dopaminergic function in the cat caudate nucleus.

摘要

我们使用经典的神经递质释放模型,研究了膳食多不饱和脂肪酸对猫尾状核切片中突触前多巴胺自身受体敏感性的影响。仅在喂食含有ω3和ω6系列δ-6-去饱和后脂肪酸饮食的动物中,观察到了[3H]多巴胺释放的最大抑制。去除其中一组或两组脂肪酸都会导致自身受体对阿扑吗啡的敏感性减弱。我们提出,需要ω3和ω6脂肪酸的平衡来维持猫尾状核中正常的多巴胺能功能。

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1
Essential fatty acids modulate apomorphine activity at dopamine receptors in cat caudate slices.必需脂肪酸调节阿扑吗啡在猫尾状核切片中多巴胺受体上的活性。
Eur J Pharmacol. 1988 May 10;149(3):317-22. doi: 10.1016/0014-2999(88)90662-0.
2
Polyenoic fatty acid deprivation of juvenile cats modulates 3H-dopamine release from presynaptic receptors in caudate slices.幼年猫多不饱和脂肪酸缺乏会调节尾状核切片中突触前受体释放3H-多巴胺。
In Vivo. 1988 May-Aug;2(3-4):295-8.
3
Stereoisomers of apomorphine differ in affinity and intrinsic activity at presynaptic dopamine receptors modulating [3H]dopamine and [3H]acetylcholine release in slices of cat caudate.阿扑吗啡的立体异构体对调节猫尾状核切片中[3H]多巴胺和[3H]乙酰胆碱释放的突触前多巴胺受体的亲和力和内在活性不同。
Eur J Pharmacol. 1983 Mar 18;88(1):81-8. doi: 10.1016/0014-2999(83)90394-1.
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Characterization of dopamine autoreceptor and [3H]spiperone binding sites in vitro with classical and novel dopamine receptor agonists.利用经典和新型多巴胺受体激动剂对多巴胺自身受体和[3H]螺哌隆结合位点进行体外表征。
Eur J Pharmacol. 1983 Mar 18;88(1):11-26. doi: 10.1016/0014-2999(83)90387-4.
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Rapid desensitization of presynaptic dopamine autoreceptors during exposure to exogenous dopamine.暴露于外源性多巴胺期间突触前多巴胺自身受体的快速脱敏
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J Neurosci. 1984 Feb;4(2):570-5. doi: 10.1523/JNEUROSCI.04-02-00570.1984.
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Interneurones are probably not involved in the presynaptic dopaminergic control of dopamine release in rabbit caudate nucleus.中间神经元可能不参与兔尾状核中多巴胺释放的突触前多巴胺能控制。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(2):129-33. doi: 10.1007/BF00504528.
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Amphetamine inhibits the electrically evoked release of [3H]dopamine from slices of the rabbit caudate.苯丙胺抑制兔尾状核切片中[3H]多巴胺的电诱发释放。
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False labelling of dopaminergic terminals in the rabbit caudate nucleus: uptake and release of [3H]-5-hydroxytryptamine.家兔尾状核中多巴胺能终末的错误标记:[3H]-5-羟色胺的摄取与释放
Br J Pharmacol. 1986 Jul;88(3):677-84. doi: 10.1111/j.1476-5381.1986.tb10250.x.

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