School of Biomedical Engineering, Department of Biomaterials, Indian Institute of Technology, Banaras Hindu University, Varanasi, India.
Department of Surgical Sciences, Anesthesiology and Intensive Care Medicine, Uppsala University Hospital, Uppsala University, SE-75185, Uppsala, Sweden.
Mol Neurobiol. 2018 Jan;55(1):312-321. doi: 10.1007/s12035-017-0743-8.
Alzheimer's disease (AD) is one of the leading causes for disability and death affecting millions of people worldwide. Thus, novel therapeutic strategies are needed to reduce brain pathology associated with AD. In view of increasing awareness regarding involvement of histaminergic pathways in AD, we explored the role of one H3 receptor inverse agonist BF 2649 and one selective H3 receptor antagonist with partial H4 agonist activity in amyloid beta peptide (AβP) infusion-induced brain pathology in a rat model. AD-like pathology was produced by administering AβP (1-40) intracerebroventricular (i.c.v.) in the left lateral ventricle (250 ng/10 μl, once daily) for 4 weeks. Control rats received saline. In separate group of rats, either BF 2649 (1 mg/kg, i.p.) or clobenpropit (1 mg/kg, i.p.) was administered once daily for 1 week after 3 weeks of AβP administration. After 30 days, blood-brain barrier (BBB) breakdown, edema formation, neuronal, glial injuries, and AβP deposits were examined in the brain. A significant reduction in AβP deposits along with marked reduction in neuronal or glial reactions was seen in the drug-treated group. The BBB breakdown to Evans blue albumin and radioiodine in the cortex, hippocampus, hypothalamus, and cerebellum was also significantly reduced in these drug-treated groups. Clobenpropit showed superior effects than the BF2649 in reducing brain pathology in AD. Taken together, our observations are the first to show that blockade of H3 and stimulation of H4 receptors are beneficial for the treatment of AD pathology, not reported earlier.
阿尔茨海默病(AD)是导致全球数百万人残疾和死亡的主要原因之一。因此,需要新的治疗策略来减少与 AD 相关的脑病理学。鉴于人们越来越意识到组胺能途径在 AD 中的参与,我们研究了一种 H3 受体反向激动剂 BF 2649 和一种具有部分 H4 激动剂活性的选择性 H3 受体拮抗剂在 AD 大鼠模型中淀粉样β肽(AβP)输注诱导的脑病理学中的作用。通过在左侧侧脑室(250ng/10μl,每日一次)中脑室内(i.c.v.)给予 AβP(1-40)4 周来产生 AD 样病理学。对照组大鼠给予生理盐水。在另一组大鼠中,在给予 AβP 3 周后,每日一次给予 BF 2649(1mg/kg,ip)或 clobenpropit(1mg/kg,ip)1 周。30 天后,检查大脑中的血脑屏障(BBB)破坏、水肿形成、神经元、神经胶质损伤和 AβP 沉积。在药物治疗组中,AβP 沉积明显减少,神经元或神经胶质反应明显减少。皮质、海马、下丘脑和小脑的 Evans 蓝白蛋白和放射性碘 125 的 BBB 破坏也明显减少。Clobenpropit 在减轻 AD 脑病理学方面的效果优于 BF2649。总之,我们的观察结果是首次表明,阻断 H3 和刺激 H4 受体对 AD 病理学的治疗有益,这在以前的研究中没有报道过。