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BAICALIN
Flacone  da 30 compresse
Euro 29,00
Integratore erboristico a base di
Puro Estratto secco di radice di
Scutellaria Baicalensis Georgi
titolo in Bioflavonoidi >95%
Per due compresse:
contenuto in Bioflavonoidi
pari a 973 mg.
     
La bibliografia scientifica inoltre riporta effetti del Flavone appartenente alla Scutellaria come

POTENTE INIBITORE DEL VIRUS

INFLUENZALE A e B

( Antiviral activity of plant flavonoid, 5,7,4'-trihydroxy-8-methoxyflavone, from the roots of Scutellaria baicalensis against influenza A (H3N2) and B viruses.(Nagai T, Suzuki Y, Tomimori T, Yamada H. Oriental Medicine Research Center, Kitasato Institute, Tokyo, Japan.

1: Biol Pharm Bull. 1995 Feb;18(2):295-9. Related Articles, 


Antiviral activity of plant flavonoid, 5,7,4'-trihydroxy-8-methoxyflavone, from the roots of Scutellaria baicalensis against influenza A (H3N2) and B viruses.

Nagai T, Suzuki Y, Tomimori T, Yamada H.

Oriental Medicine Research Center, Kitasato Institute, Tokyo, Japan.

We investigated effects of isoscutellarein-8-methylether (5,7,4'-trihydroxy-8-methoxyflavone, F36) from the roots of Scutellaria baicalensis on the single-cycle replication of mouse-adapted influenza viruses A/Guizhou/54/89 (H3N2 subtype) and B/Ibaraki/2/85 in Madin-Darby canine kidney (MDCK) cells. The agent suppressed replication of these viruses from 6 to 12 h after incubation in a dose-dependent manner by 50% at 20 microM and 90% at 40 microM, respectively. F36 (50 microM) reduced the release of B/Ibaraki virus in the medium by 90-93% when it was added to the MDCK cells at 0 to 4 h after incubation. The cell-associated virus determined by sialidase activity was also reduced by the treatment at 0 to 4 h. F36 (120 microM) inhibited the low pH-dependent membrane fusion of both the viruses with the liposome containing mixed gangliosides from bovine brain. However, the agent little affected the hemagglutination and RNA-dependent RNA polymerase activities of these viruses in vitro. These results suggest that F36 inhibits the replication of A/Guizhou and B/Ibaraki viruses at least partly by inhibiting the fusion of viral envelopes with the endosome/lysosome membrane which occurs at the early stage of the virus infection cycle. F36 (0.5 mg/kg) showed no antiviral activity against A/Guizhou and B/Ibaraki viruses in mice when administered intranasally 5 min prior to virus inoculation, whereas it significantly inhibited their proliferation in the mouse lung when administered intranasally 7 times (total 3.5 mg/kg) from 18 h before to 54 h after virus infection.

PMID: 7742801 [PubMed - indexed for MEDLINE]

 
Chem Pharm Bull (Tokyo). 1990 May;38(5):1329-32. Related Articles,


Inhibition of influenza virus sialidase and anti-influenza virus activity by plant flavonoids.

Nagai T, Miyaichi Y, Tomimori T, Suzuki Y, Yamada H.

Oriental Medicine Research Center, Kitasato Institute, Tokyo, Japan.

Flavonoids (103 species) were tested for inhibitory activity against influenza virus sialidase using sodium p-nitrophenyl-N-acetyl-alpha-D-neuraminate as substrate. 5,7,4'-Trihydroxy-8-methoxyflavone from the root of Scutellaria baicalensis showed the most potent activity (IC50, 55 microM), and this flavone appeared to be a non-competitive inhibitor of the enzyme. Whereas, negligible or weak inhibitory activities were observed for mouse liver sialidase, beta-galactosidase and alpha-mannosidase as tested. This flavone also inhibited the infection by influenza virus A/PR/8/34 of Madin-Darby canine kidney cells, and replication of the virus in the allantoic sack of embryonated egg.

These results suggest that flavone, which has potent influenza virus sialidase inhibitory activity, may have anti-influenza virus activity.

PMID: 2393958 [PubMed - indexed for MEDLINE]

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