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NT79:一种具有选择性行为作用的新型神经降压素类似物。

NT79: A novel neurotensin analog with selective behavioral effects.

机构信息

Neuropsychopharmacology Laboratory, Mayo Clinic Florida, Jacksonville, FL 32224, USA.

出版信息

Brain Res. 2010 Jan 13;1308:35-46. doi: 10.1016/j.brainres.2009.10.050. Epub 2009 Oct 27.

Abstract

Neurotensin, a tridecapeptide, is widely distributed in the brain and gastrointestinal tract. It possesses analgesic, hypothermic, and antipsychotic-like properties. Neurotensin's effects are mediated mainly through two receptor subtypes, NTS1 and NTS2. Activation of NTS1 has been implicated in most of the pharmacological effects of neurotensin but is associated with hypothermia and hypotension. We report on a novel neurotensin analog with higher selectivity to NTS2, namely, NT79, which exhibits selective behavioral effects. NT79 was tested in animal models for pain (thermal-hot plate test; visceral-acetic acid-induced writhing test), and in animal models that are predictive of antipsychotic-like effects (apomorphine-induced climbing; d-amphetamine-induced hyperactivity; disruption of prepulse inhibition). Its effects on body temperature and on blood pressure were also determined. Neurochemical changes in extracellular neurotransmitters were measured using in vivo microdialysis while the rats were simultaneously evaluated for acetic acid-induced writhing with and without pretreatment with NT79. Binding data at molecularly cloned hNTS1 and hNTS2 suggest selectivity for hNTS2. NT79 blocked the acetic acid-induced writhing with an ED(50) of 0.14 microg/kg while having no effect on thermal nociception. The writhing was paralleled by an increase in 5-HT which was attenuated by NT79. NT79 demonstrated antipsychotic-like effects by blocking apomorphine-induced climbing, d-amphetamine-induced hyperactivity, and reducing d-amphetamine- and DOI-induced disruption of prepulse inhibition. Uniquely, it caused no significant hypothermia and was without effect on blood pressure. NT79, with its higher selectivity to NTS2, may be potentially useful to treat visceral pain, and psychosis without concomitant side effects of hypothermia or hypotension.

摘要

神经降压素是一种十三肽,广泛分布于脑和胃肠道中。它具有镇痛、解热和抗精神病样作用。神经降压素的作用主要通过两种受体亚型 NTS1 和 NTS2 介导。NTS1 的激活与神经降压素的大多数药理学作用有关,但与解热和低血压有关。我们报告了一种新型神经降压素类似物,对 NTS2 具有更高的选择性,即 NT79,它表现出选择性的行为作用。NT79 在动物疼痛模型(热板试验;内脏乙酸诱导扭体试验)和预测抗精神病样作用的动物模型(阿扑吗啡诱导攀爬;d-安非他命诱导多动;前脉冲抑制破坏)中进行了测试。还确定了其对体温和血压的影响。使用体内微透析测量细胞外神经递质的神经化学变化,同时评估 NT79 预处理前后对乙酸诱导扭体的影响。在分子克隆的 hNTS1 和 hNTS2 上的结合数据表明对 hNTS2 的选择性。NT79 以 0.14μg/kg 的 ED50 阻断乙酸诱导的扭体,而对热痛觉无影响。扭体伴随着 5-HT 的增加,NT79 减弱了这种增加。NT79 通过阻断阿扑吗啡诱导的攀爬、d-安非他命诱导的多动以及减少 d-安非他命和 DOI 诱导的前脉冲抑制破坏来显示出抗精神病样作用。独特的是,它不会导致明显的解热,也不会影响血压。NT79 对 NTS2 具有更高的选择性,可能对治疗内脏疼痛和精神病有用,而不会出现解热或低血压的副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e419/2792000/25942f53dc54/nihms155350f1.jpg

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