Antiherpetic Effects ofGynura procumbens

Author:

Jarikasem Siripen12,Charuwichitratana Somyot3,Siritantikorn Sontana4,Chantratita Wasan5,Iskander Magdy6,Frahm August Wilhelm7,Jiratchariyakul Weena1

Affiliation:

1. Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, 447 Sri Ayudhya Road, Rajathevi District, Bangkok 10400, Thailand

2. Pharmaceutical and Natural Products Department, Thailand Institute of Scientific and Technological Research, Pathum Thani 12120, Thailand

3. Division of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Rama VI Road, Bangkok 10400, Thailand

4. Department of Microbiology, Faculty of Medicine Siriraj Hospital, Prannok Road, Bangkok Noi District, Bangkok 10700, Thailand

5. Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Rama VI Road, Bangkok 10400, Thailand

6. Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, Melbourne, VIC 3052, Australia

7. Department of Pharmaceutical and Medicinal Chemistry, Institute of Pharmaceutical Sciences, Freiburg University, 79104 Freiburg, Germany

Abstract

The ethanol extract ofGynura procumbensshowed virucidal and antireplicative actions against herpes simplex virus HSV-1 and HSV-2. It was further chromatographed on MCI gel CHP20P column giving the extract fractions F1 (water), F2 (water-methanol) F3 (methanol), and F4 (ethyl acetate). All but F1 had virucidal action against both viral types. We reported here the active compounds from F2 and F3. The antiherpetic compounds of F2 was a mixture of dicaffeoylquinic acids with virucidal and antireplicative actions against HSV-2 (IC5096.0 and 61.0 μg/mL, resp.) Virucidal compounds of F3 were a mixture ofβ-sitosterol and stigmasterol (IC50250.0 μg/mL against HSV-1), a mixture ofβ-sitosteryl and stigmasteryl glucosides (IC5050.0 μg/mL against HSV-2) and 1, 2-bis-dodecanoyl-3-α-D-glucopyranosyl-sn-glycerol (IC50of 40.0 μg/mL against HSV-2). Herbal products containing 1 and 2% of standardized ethanol extract were prepared. Double-blind randomized controlled clinical trial of the products was performed in patients with recurrent herpes labialis. Results showed that the number of patients, whose lesions healed within 7 days and the average healing time of both groups differed insignificantly. Viral culture on D7 indicated a decrease of infected patients from 48.7% to 7.69% in treated group whereas in placebo group the infected patients decreased from 31.25% to 20.00%. The viral reduction in treated group indicated the benefit of the product. Insignificant result might arise from a low number of participated patients and insufficient concentration of plant extract in herbal product.

Funder

Thailand Research Fund

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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