دورية أكاديمية

Arachidonic acid cascade and platelet-activating factor in the network of eye inflammatory mediators: therapeutic implications in uveitis.

التفاصيل البيبلوغرافية
العنوان: Arachidonic acid cascade and platelet-activating factor in the network of eye inflammatory mediators: therapeutic implications in uveitis.
المؤلفون: Bazan NG; Louisiana State University, Eye Center, New Orleans., de Abreu MT, Bazan HE, Belfort R Júnior
المصدر: International ophthalmology [Int Ophthalmol] 1990 Oct; Vol. 14 (5-6), pp. 335-44.
نوع المنشور: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
اللغة: English
بيانات الدورية: Publisher: Kluwer Country of Publication: Netherlands NLM ID: 7904294 Publication Model: Print Cited Medium: Print ISSN: 0165-5701 (Print) Linking ISSN: 01655701 NLM ISO Abbreviation: Int Ophthalmol Subsets: MEDLINE
أسماء مطبوعة: Publication: Dordrecht : Kluwer
Original Publication: The Hague, Junk.
مواضيع طبية MeSH: Arachidonic Acids/*metabolism , Endophthalmitis/*physiopathology , Platelet Activating Factor/*metabolism , Uveitis/*physiopathology, Animals ; Arachidonic Acid ; Arachidonic Acids/therapeutic use ; Autoimmunity ; Endophthalmitis/drug therapy ; Humans ; Hypersensitivity/immunology ; Inflammation/immunology ; Platelet Activating Factor/therapeutic use ; Uveitis/drug therapy
مستخلص: The cellular and biochemical events triggered by uveitis involve a complex array of cells and a heterogeneous network of mediators of intraocular inflammation. Resident cells are activated and inflammatory cells are recruited. Chemical mediators from the arachidonic acid cascade, prostaglandins, hydroxyeicosatetraenoic acids, and leukotrienes, are formed. Several of these metabolites are modulators of cellular functions, but when generated in sustained, excessive amounts, they contribute to enhanced vascular permeability and to the onset of pathophysiological responses. Another very active membrane-derived mediator is platelet-activating factor. This important mediator of immune and inflammatory responses may play a central role in uveitis due to cell priming, since interleukin-1, tumor necrosis factor, and other as yet unidentified mediators are also being generated. The concomitant accumulation of these networks of mediators in various parts of the uveal tract leads to spreading of the intraocular inflammatory response and cellular damage. At both early and late stages of uveitis, the generation of free radicals is also a major contributor to the impairment of function. Free radicals are generated in two distinct sites: in the oxidative burst of recruited white cells and in free radical formation and lipid peroxidation in resident cells. The identification of the cellular events that lead to the accumulation of networks of mediators of inflammation and their effects has important therapeutic implications in uveitis.
Number of References: 48
References: Br Med J. 1972 Aug 19;3(5824):452-3. (PMID: 5069222)
Am J Ophthalmol. 1980 Feb;89(2):173-9. (PMID: 7355973)
Can J Ophthalmol. 1971 Jul;6(3):205-11. (PMID: 4998497)
Invest Ophthalmol Vis Sci. 1983 Aug;24(8):1079-85. (PMID: 6135672)
Br Med J. 1977 May 28;1(6073):1387-9. (PMID: 324574)
Exp Eye Res. 1971 Mar;11(2):170-7. (PMID: 5001095)
Arch Ophthalmol. 1982 Apr;100(4):585-7. (PMID: 7041866)
Invest Ophthalmol Vis Sci. 1989 Jun;30(6):1101-3. (PMID: 2732024)
Trans Pac Coast Otoophthalmol Soc Annu Meet. 1976;57:213-21. (PMID: 1029099)
Curr Eye Res. 1984 Jan;3(1):243-52. (PMID: 6317285)
Arch Ophthalmol. 1973 Mar;89(3):217-20. (PMID: 4570752)
Arch Ophthalmol. 1981 Jun;99(6):1090-2. (PMID: 7236108)
Nat New Biol. 1972 Oct 25;239(95):248-9. (PMID: 4507809)
Biochem Biophys Res Commun. 1987 Dec 31;149(3):915-20. (PMID: 2827658)
Mod Probl Ophthalmol. 1976;16:75-9. (PMID: 765788)
Curr Eye Res. 1987 Feb;6(2):321-35. (PMID: 3471387)
Arch Ophthalmol. 1982 Mar;100(3):465-7. (PMID: 7039575)
Am J Ophthalmol. 1984 Jul 15;98(1):62-5. (PMID: 6234809)
J Immunol. 1985 Aug;135(2):1357-60. (PMID: 2861228)
Prog Clin Biol Res. 1989;312:73-84. (PMID: 2508131)
Invest Ophthalmol Vis Sci. 1982 Apr;22(4):494-501. (PMID: 7037677)
Arch Ophthalmol. 1986 May;104(5):722-4. (PMID: 3010919)
Invest Ophthalmol Vis Sci. 1984 Feb;25(2):221-3. (PMID: 6321386)
Proc Natl Acad Sci U S A. 1987 Aug;84(16):5903-7. (PMID: 3039514)
Arch Ophthalmol. 1979 Oct;97(10):1954-8. (PMID: 158354)
Br J Ophthalmol. 1981 Feb;65(2):82-8. (PMID: 7006678)
Pharmacol Rev. 1987 Jun;39(2):97-145. (PMID: 3303066)
J Pharm Pharmacol. 1987 Oct;39(10):857-9. (PMID: 2891830)
Arch Ophthalmol. 1984 Aug;102(8):1153-5. (PMID: 6331819)
Am J Ophthalmol. 1977 Jul;84(1):24-31. (PMID: 900214)
Invest Ophthalmol Vis Sci. 1987 May;28(5):886-92. (PMID: 3570697)
معلومات مُعتمدة: EY 02377 United States EY NEI NIH HHS; EY04928 United States EY NEI NIH HHS; EY06635 United States EY NEI NIH HHS
المشرفين على المادة: 0 (Arachidonic Acids)
0 (Platelet Activating Factor)
27YG812J1I (Arachidonic Acid)
تواريخ الأحداث: Date Created: 19901001 Date Completed: 19910114 Latest Revision: 20200304
رمز التحديث: 20240627
DOI: 10.1007/BF00163553
PMID: 2123479
قاعدة البيانات: MEDLINE
الوصف
تدمد:0165-5701
DOI:10.1007/BF00163553