慢性开角型青光眼血清鸢尾素水平

B. Turgut, K. Mercan, N. Ilhan, O. Çatak
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引用次数: 2

摘要

青光眼是一种进行性神经退行性疾病,其特征是视神经头(ONH)水平的视网膜神经节细胞(RGCs)轴突的丧失和视野(VF)的丧失。虽然眼压升高被认为是青光眼发病的最重要因素,但临床报告表明,仅靠降低眼压的治疗策略不足以预防所有患者的青光眼进展。因此,神经保护在青光眼的治疗中可能至关重要。3 - 6神经保护被定义为使用治疗剂来预防、减少甚至逆转因神经退行性疾病或创伤性或神经毒性损伤而导致的神经元细胞死亡。近年来的研究表明,在一些中枢神经系统(CNS)的神经退行性疾病如阿尔茨海默病(AD)中已经建立了几种神经保护治疗方法。7−11鸢尾素是一种运动诱导的112个氨基酸糖基化蛋白,由肌肉组织中纤维连接蛋白III型结构域蛋白5 (FNDC5)的蛋白水解裂解形成。已经证明鸢尾素在调节葡萄糖稳态和白色脂肪组织向棕色脂肪组织的转化中起作用。鸢尾素水平升高是能量代谢增加、体重减轻和改善葡萄糖耐量的原因。12−14鸢尾素最早是在小鼠骨骼肌中发现的,并被证明存在于许多其他组织中,包括直肠、心包、颅内动脉、心脏、舌头、视神经(ON)、小舌、大脑、卵巢、输卵管、垂体、精囊、肾上腺、食道、腔静脉、肾脏、阴茎、视网膜、睾丸、尿道、膀胱、脊髓、肝脏、小肠、扁桃体、甲状腺和阴道据报道,鸢尾素免疫反应性存在于豪猪眼睛的神经视网膜和肌肉纤维中在另一项研究中,已经证明鸢尾素的免疫反应性存在于除外核层以外的所有视网膜层以及仓鼠的角膜中
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Serum irisin levels in chronic open-angle glaucoma
Glaucoma is a progressive and neurodegenerative disease characterized by the loss of the axons of retinal ganglion cells (RGCs) at the level of the optic nerve head (ONH) and visual field (VF) loss.1,2 Although elevated intraocular pressure (IOP) is considered as most important factor in the pathogenesis of glaucoma, clinical reports demonstrate that treatment strategies on lowering IOP is not alone enough to prevent glaucoma progression in all patients. Thus, neuroprotection may be crucial in the treatment of glaucoma.3−6 Neuroprotection is defined as the use of therapeutic agents to prevent, reduce, and even to reverse neuronal cell death because of a neurodegenerative disease or a traumatic or a neurotoxic injury. Recent studies demonstrated that several neuroprotective treatments have been established in some neurodegenerative diseases of the central nervous system (CNS) disease like Alzheimer’s disease (AD).7−11 Irisin is an exercise-induced, 112-amino acid glycosylated protein that is formed by the proteolytic cleavage of fibronectin type III domain-containing protein 5 (FNDC5) in muscle tissue. It has been demonstrated that irisin works in the regulation in glucose homeostasis and the convertion of white adipose tissue to brown. Elevated irisin level increase in energy metabolism, weight loss and improves glucose tolerance causes.12−14 Irisin was firstly discovered from mouse skeletal muscle, and it was shown to be present in a variety of a lot of other tissues including rectum, pericardium, intracranial artery, heart, tongue, optic nerve (ON), uvula, brain, ovary, oviduct, pituitary, seminal vesicles, adrenal gland, esophagus, vena cava, kidney, penis, retina, testis, urethra, urinary bladder, spinal cord, liver, small intestine, tonsil, thyroid, and vagina.15 It has been reported that irisin immunoreactivity is present in the neural retina and muscle fibers in the eye of porcupine.16 In another study, it has been demonstrated that irisin immunoreactivity was found in all layers of the retina excluding the outer nuclear layer and also in the cornea in hamsters.17
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