Registro:

Referencias:

• Azher, T.N., Understanding the role of chemokines and cytokines in experimental models of herpes simplex keratitis (2017) J Immunol Res, 2017, pp. 1-5
• Biswas, P.S., Rouse, B.T., Early events in HSV keratitis-setting the stage for a blinding disease (2005) Microbes Infect, 7, pp. 799-810
• Lee, D.H., Ghiasi, H., Roles of M1 and M2 macrophages in herpes simplex virus 1 infectivity (2017) J Virol, 12, p. 91
• Kase, S., Activation of nuclear factor-kappa B in the conjunctiva with the epithelial scraping of the mouse cornea and human epidemic keratoconjunctivitis (2004) Br J Ophthalmol, 88, pp. 947-949
• Panday, A., Transcription factor NF-κB: an update on intervention strategies (2016) Arch Immunol Ther Exp (Warsz), 2016, pp. 463-483
• Austin, A., Update on the management of infectious keratitis (2017) Ophthalmology, 124, pp. 1678-1689
• Duan, R., Acyclovir-resistant corneal HSV-1 isolates from patients with herpetic keratitis (2008) J Infect Dis, 198, pp. 659-663
• Rousseau, A., Recurrent herpetic keratitis despite antiviral prophylaxis: a virological and pharmacological study (2017) Antiviral Res, 146, pp. 205-212
• Bueno, C.A., Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway (2015) Med Microbiol Immunol, 204, pp. 575-584
• Wei, P., Anti-inflammatory and antiviral activities of cynanversicoside A and cynanversicoside C isolated from Cynanchun paniculatum in influenza A virus-infected mice pulmonary microvascular endothelial cells (2017) Phytomedicine, 1, pp. 18-25
• Hassan, S.T., Bioactive natural products with anti-herpes simplex virus properties (2015) J Pharm Pharmacol, 67, pp. 1325-1336
• Son, M., Bioactive activities of natural products against herpesvirus infection (2013) J Microbiol, 51, pp. 545-551
• Sirtori, C.R., Aescin: pharmacology, pharmacokinetics and therapeutic profile (2001) Pharmacol Res, 44, pp. 183-193
• Pittler, M.H., Ernst, E., Horse chestnut seed extract for chronic venous insufficiency (2012) Cochrane Database Syst Rev, 11, p. CD003230
• Domanski, D., Molecular mechanism for cellular response to β-escin and its therapeutic implications (2016) PLoS ONE, 11
• Cheng, Y., Escin increases the survival rate of LPS-induced septic mice through inhibition of HMGB1 release from macrophages (2015) Cell Physiol Biochem, 36, pp. 1577-1586
• Liu, S., Escin inhibits lipopolysaccharide-induced inflammation in human periodontal ligament cells (2012) Mol Med Rep, 6, pp. 1150-1154
• Xin, W., Escin exerts synergistic anti-inflammatory effects with low doses of glucocorticoids in vivo and in vitro (2011) Phytomedicine, 18, pp. 272-277
• Barquero, A.A., 1-Cinnamoyl-3,11-dihydroxymeliacarpin is a natural bioactive compound with antiviral and nuclear factor-kappaB modulating properties (2006) Biochem Biophys Res Commun, 344, pp. 955-962
• Bueno, C.A., A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent (2009) Virus Res, 141, pp. 47-54
• Michelini, F.M., Synthetic stigmastanes with dual antiherpetic and immunomodulating activities inhibit ERK and Akt signaling pathways without binding to glucocorticoid receptors (2016) Biochim Biophys Acta, 1860, pp. 129-139
• Safrin, S., A rapid screen test for in vitro susceptibility of clinical herpes simplex virus isolates (1994) J Infect Dis, 169, pp. 879-882
• Howett, M.K., A broad-spectrum microbicide with virucidal activity against sexually transmitted viruses (1999) Antimicrob Agents Chemother, 43, pp. 314-321
• Wu, C.Y., Small molecules targeting severe acute respiratory syndrome human coronavirus (2004) Proc Natl Acad Sci U S A, 101, pp. 10012-10017
• Michelini, F.M., The in vitro immunomodulatory activity of a synthetic brassinosteroid analogue would account for the improvement of herpetic stromal keratitis in mice (2008) J Steroid Biochem Mol Biol, 108, pp. 164-170
• Bueno, C.A., A natural antiviral and immunomodulatory compound with antiangiogenic properties (2012) Microvasc Res, 84, pp. 235-241
• Johnson, A.C., Activation of toll-like receptor (TLR)2, TLR4, and TLR9 in the mammalian cornea induces MyD88-dependent corneal inflammation (2005) Invest Ophthalmol Vis Sci, 46, pp. 589-595
• Sarangi, P.P., Innate recognition network driving herpes simplex virus-induced corneal immunopathology: role of the toll pathway in early inflammatory events in stromal keratitis (2007) J Virol, 81, pp. 11128-11138
• Bottger, S., Melzig, M.F., The influence of saponins on cell membrane cholesterol (2013) Bioorg Med Chem, 21, pp. 7118-7124
• Ye, J., Disruption of hepatitis C virus RNA replication through inhibition of host protein geranylgeranylation (2003) Proc Natl Acad Sci U S A, 100, pp. 15865-15870
• Whitmarsh, A.J., Transcription factor AP-1 regulation by mitogen-activated protein kinase signal transduction pathways (1996) J Mol Med (Berl), 74, pp. 589-607
• Wang, X.H., Effect of beta-escin sodium on endothelial cells proliferation, migration and apoptosis (2008) Vascul Pharmacol, 49, pp. 158-165

Citas:

---------- APA ----------

---------- CHICAGO ----------

---------- MLA ----------

---------- VANCOUVER ----------