|
Some Clinic Studies on Red marine Algae and other Seaweeds and Viruses
The observations from the present study indicate that vaginal formulations of the sulfated polysaccharide carrageenan are highly effective in protecting mice from herpes simplex virus type 2 (HSV-2) infection.
Date: 11/3/2006 10:49:36 PM ( 18 y ) ... viewed 5673 times Some Clinical Studies on the Effects of
Red Marine Algae and Other Seaweeds On Viruses
Some Unaffiliated Studies on Red Marine Algae and Other Seaweeds
This is a Partial Collection of Studies, There are Many More. I have always used Red marine Algae and Other Seaweeds as the foundation of my Antiviral gels and I know also inlcude these seaweeds in my men's and women's immune formulas.
My Red Marine Algae Sex Gel is now included as part of every sexually active woman's monthly protocol, and is available by request for all my male patients at no additional charge. http://www.antiviralgel.com
Clin Diagn Lab Immunol. 1997 July; 4 (4): 465–468
Vaginal formulations of carrageenan protect mice from herpes simplex virus infection.
V R Zacharopoulos and D M Phillips
Population Council, New York, New York 10021, USA.
This article has been cited by other articles in PMC.
Abstract
The observations from the present study indicate that vaginal formulations of the sulfated polysaccharide carrageenan are highly effective in protecting mice from herpes simplex virus type 2 (HSV-2) infection. Test formulations were placed in the vaginas of progestin-treated mice prior to inoculation with HSV-2. Infection was determined by the presence of inflammation in the genital region and death. At a dose of virus that infected half of the control animals, 1% solutions of either lambda, kappa, or iota carrageenan prevented infection of almost all of the animals. Concentrations as low as 0.05% protected a large majority of the mice. At a dose of virus that infected all of the control mice, 1% solutions of carrageenans protected 85% of the inoculated mice. Other sulfated polysaccharides were less effective or showed no efficacy in preventing HSV-2 infection. These findings suggest that a vaginal formulation of carrageenan may be effective in blocking sexua| transmission of HSV-2 in women.
Carrageenan Is a Potent Inhibitor of Papillomavirus Infection
Christopher B. Buck1, Cynthia D. Thompson1, Jeffrey N. Roberts1, Martin Muller2, Douglas R. Lowy1, John T. Schiller1*
1 Laboratory of Cellular Oncology, National Cancer Institute, Bethesda, Maryland, United States of America, 2 Forschungsschwerpunkt fur Angewandte Tumorvirologie,
Deutsches Krebsforschungszentrum, Heidelberg, Germany
Certain sexually transmitted human papillomavirus (HPV) types are causally associated with the development of
cervical cancer. Our recent development of high-titer HPV pseudoviruses has made it possible to perform high-
throughput in vitro screens to identify HPV infection inhibitors. Comparison of a variety of compounds revealed that
carrageenan, a type of sulfated polysaccharide extracted from red algae, is an extremely potent infection inhibitor for a broad range of sexually transmitted HPVs. Although carrageenan can inhibit herpes simplex viruses and some strains of HIV in vitro, genital HPVs are about a thousand-fold more susceptible, with 50% inhibitory doses in the low ng/ml range. Carrageenan acts primarily by preventing the binding of HPV virions to cells. This finding is consistent with the fact that carrageenan resembles heparan sulfate, an HPV cell-attachment factor. However, carrageenan is three orders of magnitude more potent than heparin, a form of cell-free heparan sulfate that has been regarded as a highly effective model HPV inhibitor. Carrageenan can also block HPV infection through a second, postattachment heparan sulfate–independent effect. Carrageenan is in widespread commercial use as a thickener in a variety of cosmetic and food products, ranging from sexua| lubricants to infant feeding formulas. Some of these products block HPV infectivity
in vitro, even when diluted a million-fold. Clinical trials are needed to determine whether carrageenan-based products are effective as topical microbicides against genital HPVs.
Citation: Buck CB, Thompson CD, Roberts JN, Muller M, Lowy DR, et al. (2006) Carrageenan is a potent inhibitor of papillomavirus infection. PLoS Pathog 2(7): e69. DOI: 10.
1371/journal.ppat.0020069
Antiherpetic activity and mode of action of natural carrageenans of diverse structural types.
Carlucci MJ, Ciancia M, Matulewicz MC, Cerezo AS, Damonte EB.
Departamento de Quimica Biologica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Argentina.
The lambda-carrageenan 1T1, the kappa/iota-carrageenan 1C1 and the mu/nu-type 1C3, isolated from the red seaweed Gigartina skottsbergii, proved to be potent and selective inhibitors of herpes simplex virus (HSV) types 1 and 2. The antiviral IC50 values determined by virus yield inhibition assay in different cell lines ranged from 0.4 to 3.3 microg/ml, and no cytotoxic effects, measured by trypan blue exclusion on stationary or proliferating cells, tetrazolium salt method or cell protein synthesis, were observed. Time of addition and attachment studies suggested that the main target for antiviral action of the three carrageenans was virus adsorption, whereas no effect on virus internalization, or early or late protein synthesis was detected. However, the lambda-carrageenan 1T1 was still significantly inhibitory when added any time after adsorption. The pretreatment of virions with the carrageenans showed that 1C1 and 1C3 lacked direct inactivating effect at concentrations near the antiviral IC50 but 1T1 exerted virucidal action. The cyclization of 1T1 to afford the derivative 1T1T1 maintained the antiviral activity but eliminated the virucidal properties. Thus, the structure of 1T1 seems to be responsible for its differential behavior from 1C1 and 1C3, probably allowing a more stable binding to HSV, leading to virion inactivation. In contrast, 1C1 and 1C3 fail to bind with high affinity to virus alone, but are able to interfere with the interaction between HSV particles and the cell.
PMID: 10517311 [PubMed - indexed for MEDLINE]
Antiviral properties of fucoidan fractions from Leathesia difformis.
Feldman SC, Reynaldi S, Stortz CA, Cerezo AS, Damont EB.
Departamento de Quimica Organica-CIHIDECAR, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Argentina.
Three fractions of fucoidans isolated from the brown seaweed Leathesia difformis (Ee, Ec and Ea) were found to be selective antiviral agents against herpes simplex virus (HSV) types 1 and 2 and human cytomegalovirus. Fraction Ea was the most active, with IC50 values in the range 0.5-1.9 microg/ml without affecting cell viability at concentrations up to 400 microg/ml. The antiherpetic activity of Ea was assessed by three different methods, plaque reduction, inhibition of virus yield and prevention of HSV-2 induced shut-off of cell protein synthesis, demonstrating that the inhibitory effect was independent of the antiviral assay and the multiplicity of infection. The mode of action of Ea could be ascribed to an inhibitory action on virus adsorption. The fucoidans did not inhibit the blood coagulation process even at concentrations exceeding more than 100 times the IC50 value.
PMID: 11962540 [PubMed - indexed for MEDLINE]
Anti-herpes simplex virus activity of sulfated galactans from the red seaweeds Gymnogongrus griffithsiae and Cryptonemia crenulata.
Talarico LB, Zibetti RG, Faria PC, Scolaro LA, Duarte ME, Noseda MD, Pujol CA,Damonte EB.
Laboratorio de Virologia, Departamento de Quimica Biologica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon 2, 1428 Buenos Aires, Argentina.
This study presents the chemical composition and antiviral activity against herpes simplex virus type 1 (HSV-1) and 2 (HSV-2) of sulfated galactan crude extracts and main fractions obtained from two red seaweeds collected in Brazil, Gymnogongrus griffithsiae and Cryptonemia crenulata. Most of the eighteen tested products, including homogeneous kappa/iota/nu carrageenan and DL-galactan hybrid, exhibited antiherpetic activity with inhibitory concentration 50% (IC50) values in the range 0.5-5.6 microg/ml, as determined in a virus plaque reduction assay in Vero cells. The galactans lacked cytotoxic effects and showed a broad spectrum of antiviral activity against HSV-1 and HSV-2. No direct virus inactivation was observed after virion treatment with the galactans. The mode of action of these compounds could be mainly ascribed to an inhibitory effect on virus adsorption. Most importantly, a significant protection against a murine vaginal infection with HSV-2 was afforded by topical treatment with the sulfated galactans. Copyright 2004 Elsevier B.V.
PMID: 15178011 [PubMed - indexed for MEDLINE]
1: Chemotherapy. 1996 Jan-Feb;42(1):57-64. Links
Herpes simplex virus-inhibitory sulfated xylogalactans from the red seaweed Nothogenia fastigiata.
Damonte EB, Matulewicz MC, Cerezo AS, Coto CE.
Departamento de Quimica Biologica, Universidad de Buenos Aires, Argentina.
Two sulfated xylogalactans (F1 and F7), isolated from the red seaweed Nothogenia fastigiata, achieved a dose-dependent inhibition of the replication of herpes simplex virus type 1 (HSV-1) in Vero cells, with 50% effective doses in the range of 15.0-32.6 micrograms/ml, and without affecting cell viability at concentrations up to 200 micrograms/ml. The presence of sulfate groups in the molecule was essential for the antiviral properties of these polysaccharides. F7 afforded significant inhibition in HSV-1 yield if added to the cell cultures simultaneously with virus inoculum, but had no effect when it was added after 1 h of infection. Analysis of the early events of the viral replicative cycle showed that the anti-HSV effect of F7 was due to a specific inhibition of virus attachment to the host cell whereas virus internalization was not impaired.
PMID: 8751267 [PubMed - indexed for MEDLINE
Evaluation of Antiviral Activity of Virucept Red Marine Algae against Herpes Simplex Viruses (HSV)
Y. GONG(1), R. ROBERTS(2), I. GADAWSKI(1), D. CHEUNG(1), T. TAM(1), AND S.L. SACKS(1)
(1) Viridae Clinical Sciences, Inc. and The University of British Columbia, Vancouver, B.C.
(2) Bryant Nutrients, 4133 Greenwell St., Baton Rouge, LA 70805, USA
The antiviral effect of Virucept Red Marine Algae (Virucept) against HSV was evaluated in cultured Vero cells using plague reduction assay. The crude extracts containing polysaccharide were prepared by ethanol precipitation. Pre-treatment of cells with the Virucept extracts showed a strong inhibitory effect against both HSV type 1 and 3 with the 90% effective concentrations (EC90) ~0.1% for HSV-1 and 0.01% for HSV-2, respectively. Strong inhibition was also observed even after removing the extracts by washing with PBS on pre-treated cells. Similar activities were examined on HSV Acyclovir-or Forscanet-resistant strains. Approximately 66% inhibition was observed on cells that were already infected with HSV-1. Approximately 20-36% inhibition at a concentration of 0.5% was seen on HSV-2 and Acyclovir-or Forscarnet-resistant HSV infected cells. Our data indicate that the extracts from Virucept Red Marine Algae can be further developed as a vaginal microbicide for preventing HSV infection.
Inhibition of Herpesvirus Replication by Marine Algae Extracts
E. FRANK DEIG, DOUGLAS W. EHRESMANN, MELVIN T. HATCH, AND
DELIMAR J. RIEDLINGER
Naval Biomedical Research Laboratory, School of Public Health,
University of California, Berkeley, California 94720
Received for publication 8 August 1974.
Extracts from two species of marine red algae, Cryptosyphonia
woodii and Farlowia mollis, specifically inhibited herpes simplex
virus replicaton in vitro.
American Society for Microbiology, Vol. 6, No. 4, Copyright 1974
Antiviral Activity of Extracts from Marine Algae
JAMES T. RICHARDS, EARL R. KERN, LOWELL A. GLASGOW, JAMES C.
OVERALL, JR., E. FRANK DEIGN, AND MELVIN T. HATCH
Department of Pediatrics, University of Utah College of Medicine, Salt
Lake City, Utah 84132, and Naval Biosciences Laboratory, School of
Public Health, University of California, Berkeley, California 94720
Received for publication 2 March 1978
Extracts of two species of marine algae, Constantinea simplex and
Farlowia mollis, were tested for antiviral activity in tissue culture and
in experimental infections of mice. Treatment of confluent mouse embryo
fibroblast cell monolayers with either compound before viral inoculation
was effective in inhibiting the replication of herpes simplex virus type 1
and type 2, vaccinia virus, and vesicular stomatitis virus, but not
encephalomyocarditis virus, Semiliki Forest virus, or murine
cytomegalovirus. Prophylactic administration of these extracts was
effective in reducing final mortality or prolonging the mean day of death
of animals inoculated by the intraperitoneal, intracerebral, or intranasal
routes with herpes simplex virus type 2. When therapy was initiated
after viral inoculation or at a site other than that of viral inoculation, no
significant effect on mortality or on mean day of death was observed.
Neither preparation was effective in mice inoculated intraperitoneally
with encepthalomyocarditis virus, Semliki Forest virus, or murine
cytomegalovirus or in animals infected intravaginally with herpes
simplex virus type 2. The prophylactic but not therapeutic antiviral
activity of these preparations seriously limits their potential use in
human herpes simplex virus infections.
American Society for Microbiology, Vol. 14, No. 4, Copyright 1978
Further Studies on the Chemical Composition and an Initial In Vivo
Evaluation of Antiviral Material in Extracts of Macroscopic Marine Algae.
M. T. Hatch, D. W. Ehresmann, E. F. Deig, and N. A. Vedros
Naval Biosciences Laboratory, School of Public Health, University of
California, Berkeley, California 94720
Previous studies have demonstrated that the antiviral material in extracts
of 8 related species of Rhodophyta is a structural polysaccharide. The
present study extends our knowledge of chemical and biological properties
of the active material. The observation that concanavalin A (Con A)
formed an insoluable complex with antiviral molecules resulted in
development of a rapid in vitro titration procedure. Although purified
active fractions had polysaccharides containing 20% sulfate in ester form,
the material differed from other algal sulfated polysaccarides in that it
was specific for herpesvirus whereas carrageenins had a wide antiviral
spectrum. The reaction between Con A and the anti-herpesvirus
polysaccharide indicated the presence of alpha-D-glycosyl and sterically
related residues. Purified fractions were also tested for activity in cell
cultures and in mice subsequently infected with herpesvirus type 1 and 2.
Significant protection occurred when the material was administered to
mice prior to, or at the same time as virus.
Antiviral carbohydrates from marine red algae
Michael Neushul
Department of Biological Sciences, University of California, Santa Barbara,
93106, USA and Neushul Mariculature Incorporated, 475 Kellogg Way,
Goleta, CA, 93117, USA
It is possible that heparin-like sulfated polysaccharides from red algae,
or fractions thereof, might be found to be low-cost, broad-spectrum
antiviral agents. The prevailing view among virologists has been that
sulfated polysaccharides inhibit viral action by acting only at the sufraces
of cells. This perception now is changing with the finding that both the
herpes virus (containing DNA) and human immunodeficiency virus
(containing RNA) are inhibited by sulfated polysaccharides that act
within the cell as well as external to it. Aqueous extracts of many
red algae are active against retroviruses. Carrageenan, a common cell
wall polysaccharide from red algae, is co-internalized into infected cells
with the Herpes simplex virus (HSV), inhibiting the virus. Carrageenan
also interferes with fusion (syncytium formation) between cells infected
with the human immunodeficiency virus (HIV) and inhibits the specific
retroviral enzyme reverse transcriptase.
Add This Entry To Your CureZone Favorites! Print this page
Email this page
 Alert Webmaster
|
