Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection
Identifieur interne : 000221 ( PascalFrancis/Corpus ); précédent : 000220; suivant : 000222Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection
Auteurs : MIN ZHUANG ; HONG JIANG ; Yasuhiro Suzuki ; XIAOGUANG LI ; PENG XIAO ; Takashi Tanaka ; HONG LING ; BAOFENG YANG ; Hiroki Saitoh ; LIANFENG ZHANG ; CHUAN QIN ; Kazuo Sugamura ; Toshio HattoriSource :
- Antiviral research [ 0166-3542 ] ; 2009.
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English descriptors
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Abstract
We found that the butanol fraction of Cinnamomi Cortex (CC/Fr.2) showed moderate inhibitory activity in wild-type severe acute respiratory syndrome coronavirus (wtSARS-CoV) and HIV/SARS-CoV S pseudovirus infections. The inhibition on pseudovirus was also seen in cells pretreated with the CC and CC/Fr.2 (IC50S, 283.4 ± 16.3 and 149.5 ± 13.5 μg/ml, respectively), however the highest activities on wtSARS-CoV were observed when the viruses were treated by the extracts before challenging (IC50S, 43.1 ±2.8 and 7.8 ± 0.3 μg/ml; SIs, 8.4 and 23.1, respectively). Among the compounds fractionated from CC, procyanidin A2 and procyanidin B1 showed moderate anti-wtSARS-CoV activity (IC50S, 29.9 ± 3.3 and 41.3 ± 3.4 μM; SIs, 37.35 and 15.69, respectively). We also sought to determine whether they could interfere with the clathrin-dependent endocytosis pathway using transferrin receptor (TfR) as an indicator. CC/Fr.2 inhibited the internalization of TfR but the procyanidins did not. Taken together, CC/Fr.2 contains unknown substances, that could inhibit the infection, probably by interfering with endocytosis, and it also contains procyanidins that did not inhibit the internalization but inhibited the infection. Therefore, CC extracts contain anti-virus activities that act through distinct mechanisms according to differences in the compounds or mixtures.
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Format Inist (serveur)
NO : | PASCAL 09-0210832 INIST |
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ET : | Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection |
AU : | MIN ZHUANG; HONG JIANG; SUZUKI (Yasuhiro); XIAOGUANG LI; PENG XIAO; TANAKA (Takashi); HONG LING; BAOFENG YANG; SAITOH (Hiroki); LIANFENG ZHANG; CHUAN QIN; SUGAMURA (Kazuo); HATTORI (Toshio) |
AF : | Division of Emerging Infectious Diseases, Department of Internal Medicine, Tohoku University/980-8574/Japon (1 aut., 3 aut., 4 aut., 5 aut., 9 aut., 13 aut.); Department of Medical Microbiology, Harbin Medical University/Harbin, 150086/Chine (1 aut., 7 aut.); Institute of Laboratory Animal Science, Chinese Academy of Medical Science/Beijing, 100021/Chine (2 aut., 10 aut., 11 aut.); Graduate School of Biomedical Sciences, Nakasaki University/Nakasaki, 852-8131/Japon (6 aut.); Department of Pharmacology, Harbin Medical University/Harbin, 150086/Chine (8 aut.); Department of Immunology, Tohoku University/980-8574/Japon (12 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Antiviral research; ISSN 0166-3542; Coden ARSRDR; Pays-Bas; Da. 2009; Vol. 82; No. 1; Pp. 73-81; Bibl. 3/4 p. |
LA : | Anglais |
EA : | We found that the butanol fraction of Cinnamomi Cortex (CC/Fr.2) showed moderate inhibitory activity in wild-type severe acute respiratory syndrome coronavirus (wtSARS-CoV) and HIV/SARS-CoV S pseudovirus infections. The inhibition on pseudovirus was also seen in cells pretreated with the CC and CC/Fr.2 (IC50S, 283.4 ± 16.3 and 149.5 ± 13.5 μg/ml, respectively), however the highest activities on wtSARS-CoV were observed when the viruses were treated by the extracts before challenging (IC50S, 43.1 ±2.8 and 7.8 ± 0.3 μg/ml; SIs, 8.4 and 23.1, respectively). Among the compounds fractionated from CC, procyanidin A2 and procyanidin B1 showed moderate anti-wtSARS-CoV activity (IC50S, 29.9 ± 3.3 and 41.3 ± 3.4 μM; SIs, 37.35 and 15.69, respectively). We also sought to determine whether they could interfere with the clathrin-dependent endocytosis pathway using transferrin receptor (TfR) as an indicator. CC/Fr.2 inhibited the internalization of TfR but the procyanidins did not. Taken together, CC/Fr.2 contains unknown substances, that could inhibit the infection, probably by interfering with endocytosis, and it also contains procyanidins that did not inhibit the internalization but inhibited the infection. Therefore, CC extracts contain anti-virus activities that act through distinct mechanisms according to differences in the compounds or mixtures. |
CC : | 002B02S05 |
FD : | Extrait; Virus syndrome respiratoire aigu sévère; Infection; Origine végétale; Plante médicinale; Transferrine; Récepteur biologique; Activité biologique; Antiviral; Cinnamomum; Lentivirus; In vitro |
FG : | Coronavirus; Coronaviridae; Nidovirales; Virus; Lauraceae; Dicotyledones; Angiospermae; Spermatophyta; Retroviridae; Pharmacognosie |
ED : | Extract; Severe acute respiratory syndrome virus; Infection; Plant origin; Medicinal plant; Transferrin; Biological receptor; Biological activity; Antiviral; Cinnamomum; Lentivirus; In vitro |
EG : | Coronavirus; Coronaviridae; Nidovirales; Virus; Lauraceae; Dicotyledones; Angiospermae; Spermatophyta; Retroviridae; Pharmacognosy |
SD : | Extracto; Severe acute respiratory syndrome virus; Infección; Origen vegetal; Planta medicinal; Transferrina; Receptor biológico; Actividad biológica; Antiviral; Cinnamomum; Lentivirus; In vitro |
LO : | INIST-18839.354000184929350100 |
ID : | 09-0210832 |
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Pascal:09-0210832Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection</title>
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<author><name sortKey="Baofeng Yang" sort="Baofeng Yang" uniqKey="Baofeng Yang" last="Baofeng Yang">BAOFENG YANG</name>
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<author><name sortKey="Saitoh, Hiroki" sort="Saitoh, Hiroki" uniqKey="Saitoh H" first="Hiroki" last="Saitoh">Hiroki Saitoh</name>
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<author><name sortKey="Sugamura, Kazuo" sort="Sugamura, Kazuo" uniqKey="Sugamura K" first="Kazuo" last="Sugamura">Kazuo Sugamura</name>
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<author><name sortKey="Hattori, Toshio" sort="Hattori, Toshio" uniqKey="Hattori T" first="Toshio" last="Hattori">Toshio Hattori</name>
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<sZ>3 aut.</sZ>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antiviral</term>
<term>Biological activity</term>
<term>Biological receptor</term>
<term>Cinnamomum</term>
<term>Extract</term>
<term>In vitro</term>
<term>Infection</term>
<term>Lentivirus</term>
<term>Medicinal plant</term>
<term>Plant origin</term>
<term>Severe acute respiratory syndrome virus</term>
<term>Transferrin</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Extrait</term>
<term>Virus syndrome respiratoire aigu sévère</term>
<term>Infection</term>
<term>Origine végétale</term>
<term>Plante médicinale</term>
<term>Transferrine</term>
<term>Récepteur biologique</term>
<term>Activité biologique</term>
<term>Antiviral</term>
<term>Cinnamomum</term>
<term>Lentivirus</term>
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<front><div type="abstract" xml:lang="en">We found that the butanol fraction of Cinnamomi Cortex (CC/Fr.2) showed moderate inhibitory activity in wild-type severe acute respiratory syndrome coronavirus (wtSARS-CoV) and HIV/SARS-CoV S pseudovirus infections. The inhibition on pseudovirus was also seen in cells pretreated with the CC and CC/Fr.2 (IC<sub>50S</sub>
, 283.4 ± 16.3 and 149.5 ± 13.5 μg/ml, respectively), however the highest activities on wtSARS-CoV were observed when the viruses were treated by the extracts before challenging (IC<sub>50S</sub>
, 43.1 ±2.8 and 7.8 ± 0.3 μg/ml; SIs, 8.4 and 23.1, respectively). Among the compounds fractionated from CC, procyanidin A2 and procyanidin B1 showed moderate anti-wtSARS-CoV activity (IC<sub>50S</sub>
, 29.9 ± 3.3 and 41.3 ± 3.4 μM; SIs, 37.35 and 15.69, respectively). We also sought to determine whether they could interfere with the clathrin-dependent endocytosis pathway using transferrin receptor (TfR) as an indicator. CC/Fr.2 inhibited the internalization of TfR but the procyanidins did not. Taken together, CC/Fr.2 contains unknown substances, that could inhibit the infection, probably by interfering with endocytosis, and it also contains procyanidins that did not inhibit the internalization but inhibited the infection. Therefore, CC extracts contain anti-virus activities that act through distinct mechanisms according to differences in the compounds or mixtures.</div>
</front>
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<fA11 i1="05" i2="1"><s1>PENG XIAO</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>TANAKA (Takashi)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>HONG LING</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>BAOFENG YANG</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>SAITOH (Hiroki)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>LIANFENG ZHANG</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>CHUAN QIN</s1>
</fA11>
<fA11 i1="12" i2="1"><s1>SUGAMURA (Kazuo)</s1>
</fA11>
<fA11 i1="13" i2="1"><s1>HATTORI (Toshio)</s1>
</fA11>
<fA14 i1="01"><s1>Division of Emerging Infectious Diseases, Department of Internal Medicine, Tohoku University</s1>
<s2>980-8574</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>9 aut.</sZ>
<sZ>13 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Medical Microbiology, Harbin Medical University</s1>
<s2>Harbin, 150086</s2>
<s3>CHN</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Institute of Laboratory Animal Science, Chinese Academy of Medical Science</s1>
<s2>Beijing, 100021</s2>
<s3>CHN</s3>
<sZ>2 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Graduate School of Biomedical Sciences, Nakasaki University</s1>
<s2>Nakasaki, 852-8131</s2>
<s3>JPN</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Department of Pharmacology, Harbin Medical University</s1>
<s2>Harbin, 150086</s2>
<s3>CHN</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="06"><s1>Department of Immunology, Tohoku University</s1>
<s2>980-8574</s2>
<s3>JPN</s3>
<sZ>12 aut.</sZ>
</fA14>
<fA20><s1>73-81</s1>
</fA20>
<fA21><s1>2009</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>18839</s2>
<s5>354000184929350100</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2009 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>3/4 p.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>09-0210832</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Antiviral research</s0>
</fA64>
<fA66 i1="01"><s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>We found that the butanol fraction of Cinnamomi Cortex (CC/Fr.2) showed moderate inhibitory activity in wild-type severe acute respiratory syndrome coronavirus (wtSARS-CoV) and HIV/SARS-CoV S pseudovirus infections. The inhibition on pseudovirus was also seen in cells pretreated with the CC and CC/Fr.2 (IC<sub>50S</sub>
, 283.4 ± 16.3 and 149.5 ± 13.5 μg/ml, respectively), however the highest activities on wtSARS-CoV were observed when the viruses were treated by the extracts before challenging (IC<sub>50S</sub>
, 43.1 ±2.8 and 7.8 ± 0.3 μg/ml; SIs, 8.4 and 23.1, respectively). Among the compounds fractionated from CC, procyanidin A2 and procyanidin B1 showed moderate anti-wtSARS-CoV activity (IC<sub>50S</sub>
, 29.9 ± 3.3 and 41.3 ± 3.4 μM; SIs, 37.35 and 15.69, respectively). We also sought to determine whether they could interfere with the clathrin-dependent endocytosis pathway using transferrin receptor (TfR) as an indicator. CC/Fr.2 inhibited the internalization of TfR but the procyanidins did not. Taken together, CC/Fr.2 contains unknown substances, that could inhibit the infection, probably by interfering with endocytosis, and it also contains procyanidins that did not inhibit the internalization but inhibited the infection. Therefore, CC extracts contain anti-virus activities that act through distinct mechanisms according to differences in the compounds or mixtures.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B02S05</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Extrait</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Extract</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Extracto</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Virus syndrome respiratoire aigu sévère</s0>
<s2>NW</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Severe acute respiratory syndrome virus</s0>
<s2>NW</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Severe acute respiratory syndrome virus</s0>
<s2>NW</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Infection</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Infection</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Infección</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Origine végétale</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Plant origin</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Origen vegetal</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Plante médicinale</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Medicinal plant</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Planta medicinal</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Transferrine</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Transferrin</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Transferrina</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Récepteur biologique</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Biological receptor</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Receptor biológico</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Activité biologique</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Biological activity</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Actividad biológica</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Antiviral</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Antiviral</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Antiviral</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Cinnamomum</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Cinnamomum</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Cinnamomum</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Lentivirus</s0>
<s2>NW</s2>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Lentivirus</s0>
<s2>NW</s2>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Lentivirus</s0>
<s2>NW</s2>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>In vitro</s0>
<s5>13</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Coronavirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Lauraceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Lauraceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Lauraceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Pharmacognosie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Pharmacognosy</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Farmacognosia</s0>
<s5>37</s5>
</fC07>
<fN21><s1>152</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 09-0210832 INIST</NO>
<ET>Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection</ET>
<AU>MIN ZHUANG; HONG JIANG; SUZUKI (Yasuhiro); XIAOGUANG LI; PENG XIAO; TANAKA (Takashi); HONG LING; BAOFENG YANG; SAITOH (Hiroki); LIANFENG ZHANG; CHUAN QIN; SUGAMURA (Kazuo); HATTORI (Toshio)</AU>
<AF>Division of Emerging Infectious Diseases, Department of Internal Medicine, Tohoku University/980-8574/Japon (1 aut., 3 aut., 4 aut., 5 aut., 9 aut., 13 aut.); Department of Medical Microbiology, Harbin Medical University/Harbin, 150086/Chine (1 aut., 7 aut.); Institute of Laboratory Animal Science, Chinese Academy of Medical Science/Beijing, 100021/Chine (2 aut., 10 aut., 11 aut.); Graduate School of Biomedical Sciences, Nakasaki University/Nakasaki, 852-8131/Japon (6 aut.); Department of Pharmacology, Harbin Medical University/Harbin, 150086/Chine (8 aut.); Department of Immunology, Tohoku University/980-8574/Japon (12 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Antiviral research; ISSN 0166-3542; Coden ARSRDR; Pays-Bas; Da. 2009; Vol. 82; No. 1; Pp. 73-81; Bibl. 3/4 p.</SO>
<LA>Anglais</LA>
<EA>We found that the butanol fraction of Cinnamomi Cortex (CC/Fr.2) showed moderate inhibitory activity in wild-type severe acute respiratory syndrome coronavirus (wtSARS-CoV) and HIV/SARS-CoV S pseudovirus infections. The inhibition on pseudovirus was also seen in cells pretreated with the CC and CC/Fr.2 (IC<sub>50S</sub>
, 283.4 ± 16.3 and 149.5 ± 13.5 μg/ml, respectively), however the highest activities on wtSARS-CoV were observed when the viruses were treated by the extracts before challenging (IC<sub>50S</sub>
, 43.1 ±2.8 and 7.8 ± 0.3 μg/ml; SIs, 8.4 and 23.1, respectively). Among the compounds fractionated from CC, procyanidin A2 and procyanidin B1 showed moderate anti-wtSARS-CoV activity (IC<sub>50S</sub>
, 29.9 ± 3.3 and 41.3 ± 3.4 μM; SIs, 37.35 and 15.69, respectively). We also sought to determine whether they could interfere with the clathrin-dependent endocytosis pathway using transferrin receptor (TfR) as an indicator. CC/Fr.2 inhibited the internalization of TfR but the procyanidins did not. Taken together, CC/Fr.2 contains unknown substances, that could inhibit the infection, probably by interfering with endocytosis, and it also contains procyanidins that did not inhibit the internalization but inhibited the infection. Therefore, CC extracts contain anti-virus activities that act through distinct mechanisms according to differences in the compounds or mixtures.</EA>
<CC>002B02S05</CC>
<FD>Extrait; Virus syndrome respiratoire aigu sévère; Infection; Origine végétale; Plante médicinale; Transferrine; Récepteur biologique; Activité biologique; Antiviral; Cinnamomum; Lentivirus; In vitro</FD>
<FG>Coronavirus; Coronaviridae; Nidovirales; Virus; Lauraceae; Dicotyledones; Angiospermae; Spermatophyta; Retroviridae; Pharmacognosie</FG>
<ED>Extract; Severe acute respiratory syndrome virus; Infection; Plant origin; Medicinal plant; Transferrin; Biological receptor; Biological activity; Antiviral; Cinnamomum; Lentivirus; In vitro</ED>
<EG>Coronavirus; Coronaviridae; Nidovirales; Virus; Lauraceae; Dicotyledones; Angiospermae; Spermatophyta; Retroviridae; Pharmacognosy</EG>
<SD>Extracto; Severe acute respiratory syndrome virus; Infección; Origen vegetal; Planta medicinal; Transferrina; Receptor biológico; Actividad biológica; Antiviral; Cinnamomum; Lentivirus; In vitro</SD>
<LO>INIST-18839.354000184929350100</LO>
<ID>09-0210832</ID>
</server>
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