The non-antibiotic properties of tetracyclines: Clinical potential in ophthalmic disease

被引:79
作者
Federici, Thomas J. [1 ]
机构
[1] SUNY Stony Brook, Dept Ophthalmol, Hlth Sci Ctr, Stony Brook, NY 11794 USA
关键词
Chemically modified non-antibacterial tetracyclines; Choroidal neovascularization; Corneal neovascularization; Retinal neovascularization; Tetracycline; ENDOTHELIAL GROWTH-FACTOR; MATRIX-METALLOPROTEINASE ACTIVITY; MOLECULAR-WEIGHT HEPARIN; MACULAR DEGENERATION; OCULAR ROSACEA; CHOROIDAL NEOVASCULARIZATION; PHOTODYNAMIC THERAPY; DIABETIC-RETINOPATHY; CYTOKINE EXPRESSION; CHRONIC BLEPHARITIS;
D O I
10.1016/j.phrs.2011.06.013
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Beyond their decades of long use as broad-spectrum antibiotics, tetracyclines and their derivatives have been shown to exhibit non-antimicrobial properties including their ability to interact with matrix metalloproteinases (MMP), tissue inhibitors of MMPs, growth factors and cytokines. As such, they are capable of affecting inflammation, immunomodulation, cell proliferation, and angiogenesis. Although they have been used to treat a variety of conditions including acne, cutaneous sarcoid, and rheumatoid arthritis, amongst others, their use in treating ophthalmologic disease is in its infancy. Materials and methods: A literature review on the role of non-antimicrobial properties of tetracyclines, semisynthetic tetracyclines, and chemically modified non-antibacterial tetracyclines (CMTs) and their clinical properties was performed. The effects of these compounds in relation to ophthalmic disease are presented. Results: Due to their non-antimicrobial properties, tetracyclines and their derivatives are capable of influencing a wide variety of ocular diseases in animal models. By affecting expression of MMP-9 and tumor necrosis factor (TNF)-alpha, these compounds decrease corneal permeability, improve corneal smoothness, and reduce meibomian gland dysfunction; this improves the tear film which in turn restores the optical quality of the tear film and cornea. Sterile corneal ulceration may be inhibited via anticollagenase activity; this has been demonstrated in both animal models and case reports. CMTs suppress cataractogenesis in a diabetic rat model, possibly by affecting MMPs. With respect to retinal disease, tetracyclines can inhibit both microglial-mediated cell death and retinal cell apoptosis as well as prevent retinal capillary damage via caspase inhibition thus preventing retinal neovascularization. Experimental choroidal neovascularization is reduced by inhibition of MMP-2 and MMP-9, elevation of pigment epithelial derived growth factor (PEDF), and reduction of vascular endothelial growth factor (VEGF) expression via Fas ligand. Discussion: Due to their non-antimicrobial properties, tetracyclines and their derivatives are capable of influencing a wide variety of ocular disease in animal models. Research suggests that they are able to reduce inflammation in the eyelid meibomian glands, improve optical clarity of the cornea, retard cataract formation, and limit ocular angiogenesis. They may have a role in treating the leading causes of vision loss: cataract, age-related macular degeneration, and diabetic retinopathy, all of which are anticipated to increase in incidence due to the aging population. Conclusions: Tetracyclines, semisynthetic tetracyclines, and CMTs may have a role in the treatment of several important ophthalmologic diseases; however, further research is required, including prospective multicenter clinical trials. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:614 / 623
页数:10
相关论文
共 120 条
[1]
Akpek EK, 1997, OPHTHALMOLOGY, V104, P1863, DOI 10.1016/S0161-6420(97)30015-3
[2]
Age-related macular degeneration: Etiology, pathogenesis, and therapeutic strategies [J].
Ambati, J ;
Ambati, BK ;
Yoo, SH ;
Ianchulev, S ;
Adamis, AP .
SURVEY OF OPHTHALMOLOGY, 2003, 48 (03) :257-293
[3]
[Anonymous], 1986, Arch Ophthalmol, V104, P694
[4]
[Anonymous], 1981, OPHTHALMOLOGY, V88, P583
[5]
Arnold J, 2001, AM J OPHTHALMOL, V131, P541
[6]
Short term oral minocycline treatment of meibomianitis [J].
Aronowicz, J. D. ;
Shine, W. E. ;
Oral, D. ;
Vargas, J. M. ;
McCulley, J. P. .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2006, 90 (07) :856-860
[7]
Inhibition of experimental angiogenesis of cornea by various doses of doxycycline and combination of triamcinolone acetonide with low-molecular-weight heparin and doxycycline [J].
Aydin, Erdinc ;
Kivilcim, Muhamet ;
Peyman, Gholam A. ;
Esfahani, Mohammad Riazi ;
Kazi, Abdul Ahad ;
Sanders, Donald R. .
CORNEA, 2008, 27 (04) :446-453
[8]
OXYTETRACYCLINE IN THE TREATMENT OF OCULAR ROSACEA - A DOUBLE-BLIND TRIAL [J].
BARTHOLOMEW, RS ;
REID, BJ ;
CHEESBROUGH, MJ ;
MACDONALD, M ;
GALLOWAY, NR .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1982, 66 (06) :386-388
[9]
Desiccating stress decreases apical corneal epithelial cell size - Modulation by the metalloproteinase inhibitor doxycycline [J].
Beardsley, Robert M. ;
De Paiva, Cintia S. ;
Power, David F. ;
Pflugfelder, Stephen C. .
CORNEA, 2008, 27 (08) :935-940
[10]
Bhatt LK, 2010, AM J TRANSL RES, V2, P181