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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Inverse relationship of cannabimimetic (R+)WIN 55, 212 on behavior and seizure threshold during the juvenile period
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Inverse relationship of cannabimimetic (R+)WIN 55, 212 on behavior and seizure threshold during the juvenile period

机译:大麻模拟物(R +)WIN 55、212与青少年时期行为和癫痫发作阈值成反比

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Cannabinoids have anti-convulsant effects in both in vivo and in vitro models of status epilepticus. Since the development of spontaneous seizures and neuronal vulnerability are age-dependent, we hypothesized that the anti-convulsant effects of cannabimimetics are also age-dependent. We administered a single injection of varied doses of (R+)WIN 55,212 (0.5, 1, 5 mg/kg) to postnatal (P) day 20 rats 90 min prior to induction of kainate (KA)-induced status epilepticus. The highest dose of (R+)WIN 55,212 (5 mg/kg) resulted in rapid onset of behavioral stupor, loss of balance, stiffening and immobility while standing on hind legs or laying flat in prone position; lower doses had minimal or no behavioral effect. After KA administration, seizure scores and electroencephalography (EEG) recordings were inversely related to (R+)WIN 55,212 dosage whereby higher doses were associated with high seizures scores and synchronous epileptiform activity and low doses with low seizure scores and diminished spiking in the EEG. Immunohistochemistry revealed a dose-dependent reduction in CB1 receptor expression with increasing concentrations of (R+)WIN 55,212 in presence or absence of KA seizures. Nissl and NeuN staining showed hippocampal injury was attenuated only when seizures were mild following low doses of WIN 55,212 (0.5, 1 mg/kg), consistent with the level of CB1 expression. Since low doses abolished seizures without psychotropic side-effects further study may facilitate a groundbreaking cannabamimetic therapeutic strategy to treat early-life seizures. Higher doses had adverse effects on behavior and failed to prevent seizures and protect CA1 neurons possibly due to inactivation or loss of CB1 receptors.
机译:大麻素在癫痫持续状态的体内和体外模型中均具有抗惊厥作用。由于自发性癫痫发作和神经元脆弱性的发展是年龄依赖性的,因此我们假设大麻模拟物的抗惊厥作用也是年龄依赖性的。我们在诱导海藻酸盐(KA)引起的癫痫持续状态前90分钟,对出生后(P)第20天的大鼠单次注射了不同剂量的(R +)WIN 55,212(0.5,1,5 mg / kg)。 (R +)WIN 55,212的最高剂量(5 mg / kg)导致站立时后肢站立或俯卧时行为性木僵迅速发作,失去平衡,僵硬和无法活动;较低的剂量几乎没有行为影响。 KA给药后,癫痫发作评分和脑电图(EEG)记录与(R +)WIN 55,212剂量成反比,其中高剂量与高癫痫发作评分和同步癫痫样活动相关,低剂量伴有低癫痫发作分数和EEG发作减少。免疫组织化学显示,在存在或不存在KA发作的情况下,随着(R +)WIN 55,212浓度的增加,CB1受体表达呈剂量依赖性降低。 Nissl和NeuN染色显示,仅在低剂量WIN 55,212(0.5,1 mg / kg)伴随轻度癫痫发作时才减轻海马损伤,这与CB1表达水平一致。由于低剂量可消除癫痫发作而无精神副作用,因此进一步的研究可能有助于突破性的大麻模拟疗法来治疗早期发作。较高剂量可能会对行为产生不利影响,可能无法预防癫痫发作和保护CA1神经元,这可能是由于CB1受体失活或丢失所致。

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