Bimatoprost Ophthalmic Solution (BOS) 0.3 mg w/v for 1 Open Trial of Long-term Preventive Therapy of Migraine in 3 patients with Pathophysiologic Shift from Brain to Eye

Gupta Vinod Kumar
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Abstract

Known since antiquity, migraine is a complex primary disorder, an episodic painful Autonomic Nervous System (ANS) storm, generally following the stress/post-stress phase. Despite exhaustive study of neuropeptides, neurochemicals, molecules, neurogenetics, neuroimaging along with animal and human experiments over the last 50 years, the scientific basis of migraine remains unknown. Straddling eight decades from Cortical Spreading Depression (CSD) to Calcitonin-Gene Related Peptide (CGRP) and its antagonists, exponentially increasing data have failed to create a gestalt synthesis. This article lays cohesive and robust fundamental principles for the comprehension and management of migraine. The continuum between migraine and non-congestive Primary Open-Angle Glaucoma (POAG), Normal Tension Glaucoma (NTG), or Low-Tension Glaucoma (LTG) is advancing. The case of sustained remission of migraine attacks (> 75%) over 3 years - 5 years with ocular hypotensive topical Bimatoprost Ophthalmic Solution (BOS) 0.3% in an N-of-1 trial in 3 patients with refractory migraine is presented. A cause-effect-adaptive process underlies the ANS-stress/post-stress-linked biology of migraine. Vasopressin-serotonin-norepinephrine ‘homeostatic-adaptive system’ Lowers Intraocular Pressure (IOP), while enhancing anti-stress, antinociception, vasomotor, and behaviour control functions, thereby selectively decreasing algogenic neural traffic in the ophthalmic division of trigeminal nerve (V1), and, raising the threshold to develop migraine. Striking migraine headache-aborting feature of vomiting is also likely linked to a several hundred-fold increase in arginine-vasopressin secretion. Eye-cover tests and self-ocular digital displacement are essential to studying the visual aura. Real-time physical displacement of Scintillating Scotoma (SS) and floating ‘stars’ is reported. The basis of spontaneous onset and offset, self-limited duration of migraine attacks, as well as female preponderance, and age/menopause decline in prevalence, are elucidated. Intraocular implants with long-term ocular hypotensive effects, including bimatoprost, are the future of migraine management. Controlled trials are required to establish the migraine-preventive effect of topical bimatoprost, a revolutionary advance in neuroscience.
比马前列素眼科溶液(BOS)0.3 毫克/毫升,用于 3 例病理生理从脑转移至眼的偏头痛长期预防治疗开放试验
自古以来,偏头痛就是一种复杂的原发性疾病,是一种发作性自律神经系统(ANS)疼痛风暴,通常发生在压力/压力后阶段。尽管在过去 50 年中对神经肽、神经化学物质、分子、神经遗传学、神经影像学以及动物和人体实验进行了详尽的研究,但偏头痛的科学基础仍然是未知的。从皮质扩展性抑郁(CSD)到降钙素基因相关肽(CGRP)及其拮抗剂,横跨八十年的时间里,呈指数级增长的数据未能形成一个格式塔综合体。本文为偏头痛的理解和管理提供了连贯而有力的基本原则。偏头痛与非充血性原发性开角型青光眼(POAG)、正常张力性青光眼(NTG)或低张力性青光眼(LTG)之间的连续性正在不断推进。本文介绍了在一项 N-of-1 试验中,3 名难治性偏头痛患者使用眼部降压外用比马前列素眼药水(BOS)0.3% 后,偏头痛发作在 3-5 年间持续缓解(> 75%)的病例。偏头痛的自律神经系统(ANS)-应激/应激后相关生物学特性的基础是一个因果-适应过程。血管加压素-羟色胺-去甲肾上腺素 "平衡适应系统 "可降低眼压(IOP),同时增强抗应激、抗痛觉、血管运动和行为控制功能,从而有选择性地减少三叉神经眼分部(V1)的藻类神经流量,并提高偏头痛的发病阈值。呕吐可缓解偏头痛的显著特点也可能与精氨酸加压素分泌量增加几百倍有关。眼罩测试和自眼数字位移对研究视觉先兆至关重要。报告了闪烁视网膜瘤(SS)和漂浮 "星星 "的实时物理位移。阐明了偏头痛自发发作和偏移、自限性发作持续时间、女性偏多以及年龄/更年期发病率下降的基础。包括比马前列素在内的具有长期降眼压作用的眼内植入物是治疗偏头痛的未来趋势。需要进行对照试验,以确定局部用药比马前列素的偏头痛预防效果,这是神经科学的革命性进步。
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