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Potential anti-depressive effects of thyrotropin releasing hormone (TRH) and its analogues.

作者信息

Ogawa N, Mizuno S, Mori A, Nukina I, Ota Z, Yamamoto M

出版信息

Peptides. 1984 Jul-Aug;5(4):743-6. doi: 10.1016/0196-9781(84)90016-0.

DOI:10.1016/0196-9781(84)90016-0
PMID:6436797
Abstract

The anti-depressive effects of thyrotropin releasing hormone (TRH) and its analogues (DN-1417: gamma-butyrolactone-gamma-carbonyl-histidyl-prolinamide citrate; MK-771: L-pyro-2-aminoadipyl-histidyl-thiazolidine-4-carboxamide) were examined in behavioral despair rats, an animal model of depression. TRH, DN-1417, MK-771, amitriptyline and diazepam were injected three times after the first forced swimming. One hr after the last injection, a 5-min swimming test was performed. Experimental animals were placed in a Hall's type open-field apparatus immediately before and after the 5-min test, and their locomotor activities were determined. No significant difference was noted in the locomotor activity immediately before the 5-min test among any group. In the 5-min swimming test, TRH, DN-1417 and MK-771 caused a dose-dependent decrease in immobility, showing an anti-depressive effect similar to amitriptyline. Diazepam showed no difference compared with the control group. After the swimming test, locomotor activity remarkably decreased in the control rats, while decreased locomotor activity was partially prevented in the TRH, DN-1417, MK-771 and amitriptyline treated rats which exhibited active movement not only during the swimming period but also after it. In terms of the minimum effective dose, TRH and DN-1417 seemed to be of similar potency, while MK-771 was 40-fold stronger than TRH. An examination of a possible correlation between the cross-reactivity of TRH analogues in a radioreceptor assay and the effects of the analogues on despair rats suggested that the structure-binding relationship was proportional to the structure-activity relationship.

摘要

相似文献

1
Potential anti-depressive effects of thyrotropin releasing hormone (TRH) and its analogues.
Peptides. 1984 Jul-Aug;5(4):743-6. doi: 10.1016/0196-9781(84)90016-0.
2
Effects of thyrotropin releasing hormone and its analogues on unconsciousness following head injury in mice.促甲状腺素释放激素及其类似物对小鼠头部受伤后意识丧失的影响。
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Increase in rat regional brain cyclic nucleotides by thyrotropin-releasing hormone (TRH) and its analog DN-1417.促甲状腺激素释放激素(TRH)及其类似物DN - 1417使大鼠脑局部区域环核苷酸增加。
Jpn J Pharmacol. 1983 Oct;33(5):915-26. doi: 10.1254/jjp.33.915.
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Analogs of thyrotropin-releasing hormone in potentiating the spinal monosynaptic reflex in vitro.促甲状腺激素释放激素类似物在体外增强脊髓单突触反射中的作用
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Intestinal absorption mechanisms of gamma-butyrolactone-gamma-carbonyl-L-histidyl-L-prolinamide citrate (DN-1417) and thyrotropin-releasing hormone (TRH).γ-丁内酯-γ-羰基-L-组氨酰-L-脯氨酰胺柠檬酸盐(DN-1417)和促甲状腺激素释放激素(TRH)的肠道吸收机制
J Pharmacobiodyn. 1985 Apr;8(4):278-85. doi: 10.1248/bpb1978.8.278.
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Thyrotropin-releasing hormone and its analog MK-771 increase the cerebroventricular perfusate content of dihydroxyphenylacetic acid.促甲状腺激素释放激素及其类似物MK-771可增加二羟基苯乙酸的脑室灌流液含量。
J Neurochem. 1984 Aug;43(2):593-6. doi: 10.1111/j.1471-4159.1984.tb00941.x.
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Thyrotropin-releasing hormone receptor activation in the spinal cord increases blood pressure and sympathetic tone to the vasculature and the adrenals.脊髓中促甲状腺激素释放激素受体的激活会升高血压,并增加对血管和肾上腺的交感神经张力。
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Intracerebroventricular injection of a TRH analogue, gamma-butyrolactone-gamma-carbonyl-L-histidyl-prolinamide, induces gastric lesions and gastric acid stimulation in rats.向大鼠脑室内注射促甲状腺激素释放激素类似物γ-丁内酯-γ-羰基-L-组氨酰-脯氨酰胺,会诱发胃部损伤并刺激胃酸分泌。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Aug;330(2):142-6. doi: 10.1007/BF00499907.
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A possible mechanism of action of thyrotropin-releasing hormone (TRH) and its analog DN-1417 on the release of dopamine from the nucleus accumbens and striatum in rats.促甲状腺激素释放激素(TRH)及其类似物DN-1417对大鼠伏隔核和纹状体中多巴胺释放的一种可能作用机制。
Jpn J Pharmacol. 1985 Dec;39(4):425-35. doi: 10.1254/jjp.39.425.

引用本文的文献

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Design and exploratory neuropharmacological evaluation of novel thyrotropin-releasing hormone analogs and their brain-targeting bioprecursor prodrugs.新型促甲状腺激素释放激素类似物及其脑靶向生物前体前药的设计与探索性神经药理学评价。
Pharmaceutics. 2013;5(2):318-28. doi: 10.3390/pharmaceutics5020318.
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Exploratory neuropharmacological evaluation of a conformationally constrained thyrotropin-releasing hormone analogue.一种构象受限的促甲状腺激素释放激素类似物的探索性神经药理学评估。
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Electroconvulsive seizures regulate gene expression of distinct neurotrophic signaling pathways.
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J Neurosci. 2004 Mar 17;24(11):2667-77. doi: 10.1523/JNEUROSCI.5377-03.2004.
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Is the forced swimming test a suitable model for revealing antidepressant activity?强迫游泳试验是揭示抗抑郁活性的合适模型吗?
Psychopharmacology (Berl). 1988;94(2):147-60. doi: 10.1007/BF00176837.
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Effect of low intravenous doses of TRH, acid-TRH and cyclo(His-Pro) on cerebral and peripheral blood flows.静脉注射低剂量促甲状腺激素释放激素、酸性促甲状腺激素释放激素和环(组氨酸-脯氨酸)对脑血流和外周血流的影响。
Br J Pharmacol. 1986 Mar;87(3):509-19. doi: 10.1111/j.1476-5381.1986.tb10193.x.
6
Changes in the behavioural response to a TRH analogue following chronic amitriptyline treatment and repeated electroconvulsive shock in the rat.大鼠经慢性阿米替林治疗和重复电休克后对促甲状腺激素释放激素类似物行为反应的变化。
Br J Pharmacol. 1986 May;88(1):129-39. doi: 10.1111/j.1476-5381.1986.tb09479.x.