Skip to main content

Main menu

  • Home
  • Current Issue
  • Archive
  • Info for
    • Authors
    • Editorial Policies
    • Advertisers
    • Editorial Board
  • Other Publications
    • Anticancer Research
    • Cancer Genomics & Proteomics
    • Cancer Diagnosis & Prognosis
  • More
    • IIAR
    • Conferences
  • About Us
    • General Policy
    • Contact
  • Other Publications
    • In Vivo
    • Anticancer Research
    • Cancer Genomics & Proteomics

User menu

  • Register
  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
In Vivo
  • Other Publications
    • In Vivo
    • Anticancer Research
    • Cancer Genomics & Proteomics
  • Register
  • Subscribe
  • My alerts
  • Log in
  • My Cart
In Vivo

Advanced Search

  • Home
  • Current Issue
  • Archive
  • Info for
    • Authors
    • Editorial Policies
    • Advertisers
    • Editorial Board
  • Other Publications
    • Anticancer Research
    • Cancer Genomics & Proteomics
    • Cancer Diagnosis & Prognosis
  • More
    • IIAR
    • Conferences
  • About Us
    • General Policy
    • Contact
  • Visit iiar on Facebook
  • Follow us on Linkedin
Research ArticleClinical Studies

A Clinical Pilot Study of Lignin—Ascorbic Acid Combination Treatment of Herpes Simplex Virus

BLANCA SILVIA GONZALEZ LOPEZ, MASAJI YAMAMOTO, KATSUAKI UTSUMI, CHIAKI ARATSU and HIROSHI SAKAGAMI
In Vivo November 2009, 23 (6) 1011-1016;
BLANCA SILVIA GONZALEZ LOPEZ
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: gblancasilvia@yahoo.com sakagami@dent.meikai.ac.jp
MASAJI YAMAMOTO
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
KATSUAKI UTSUMI
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
CHIAKI ARATSU
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
HIROSHI SAKAGAMI
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: gblancasilvia@yahoo.com sakagami@dent.meikai.ac.jp
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

Antiviral drugs as well as natural remedies have been used to reduce symptoms and the rate of recurrences of herpes simplex virus type 1 (HSV-1) infection, a common disease. To evaluate anti-HSV-1 activity of a pine cone lignin and ascorbic acid treatment, a clinical pilot study was carried out. Forty-eight healthy patients of both genders between 4 and 61 years old (mean: 31±16 years), with active lesions of HSV-1, took part in the study. According to the HSV-1 stage at the presentation, the patients were classified into the prodromic (16 patients), erythema (11 patients), papule edema (1 patient), vesicle/pustule (13 patients) and ulcer stages (7 patients). One mg of lignin-ascorbic acid tablet or solution was orally administered three times daily for a month. Clinical evaluations were made daily the first week and at least three times a week during the second week after the onset and every six months during the subsequent year to identify recurrence episodes. The patients who began the lignin-ascorbic acid treatment within the first 48 hours of symptom onset did not develop HSV-1 characteristic lesions, whereas those patients who began the treatment later experienced a shorter duration of cold sore lesions and a decrease in the symptoms compared with previous episodes. The majority of the patients reported the reduction in the severity of symptoms and the reduction in the recurrence episodes after the lignin-ascorbic acid treatment compared with previous episodes, suggesting its possible applicability for the prevention and treatment of HSV-1 infection.

  • Ant-HSV activity
  • lignin
  • ascorbic acid
  • clinical pilot study

Herpes simplex virus 1 (HSV-1), a neurotropic virus, commonly infects the skin and mucous membranes, and remains latent before erupting in response to different stimuli (1). Lesions are often painful, burning or pruritic and tend to recur in most patients (2). The treatment of HSV-1 is based on the control, but not on the care of the disease, since the virus cannot be eradicated (3). Despite extreme variation in the severity of the lesion from patient to patient, symptoms are normally resolved in one or two weeks without treatment (4). Nevertheless, it has been suggested that antiviral drugs such as nucleoside analogs could reduce the symptoms and the recurrence rate (5-7). Clinical trials of different topical and systemic antiviral drugs, have demonstrated an effective treatment in HSV-1 infections (8-10). Acyclovir has been used as a standard regimen for the control of oral HSV-1 (5, 7, 11, 12), but produced controversial efficacy (13, 14) and a wide array of side-effects (6, 15), and even failed to prevent the secondary sunlight exposure-induced recurrence (16). Hamuy and Berman reviewed the use of a number of antiviral agents with diverse results, however, the authors emphasize that the different methods researchers had used made direct comparison difficult (17).

Lignins are major cell components formed by the dehydrogenation polymerization of three monolignols, p-coumaryl, coniferyl and sinapyl alcohols. Lignin carbohydrate complexes, Fr VI and Fr VII, from the alkaline extract of pine cones, have shown potent antiviral activity in mice via direct interaction with virus (18). Lignin carbohydrate complexes, such as alkali-lignin, lignin sulfonate and Fr VI or Fr VII, at higher concentrations, strongly enhanced both the radical intensity and cytotoxic activity of ascorbic acid (19). However, there has been no clinical report of the antiviral activity of lignin carbohydrate complex. The purpose of this study was to evaluate the effect of pine cone lignin and ascorbic acid combination treatment on the duration with lesions and the decrease of symptoms in HSV-I infected patients.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table I.

Stages of HVS lesions in the 48 study patients.

Patients and Methods

Patients. Participants were recruited among students and outpatients from the clinics of the Faculty of Dentistry of the Universidad Autonoma del Estado de Mexico. A total of 1,300 people were face to face interviewed; those with a history of HSV-1 recurrent episodes were invited to participate in the study. They were requested to attend the Oral Pathology Laboratory, when presenting a new onset. From 139 people originally invited to participate, 73 people did not attend the laboratory during the study period. Eighteen patients were lost after the treatment was started. A total sample of 48 patients, 17 male (35%) and 31 female (65%), aged from 4 to 61 years (mean: 31±16 years) with active lesions detected on presentation, participated in the study. None of the patients reported systemic disease or medicine use. This study was approved by the Institutional Ethical Committee and all the participants signed a document of informed consent.

At the start of treatment/on presentation at the laboratory, the patients were classified, according to the criteria of Paterson and Kwong (20) (Table I). To record the evolution of the HSV lesions, during the first week the patients attended the clinic daily from Monday to Friday, and during the second week they attended three times. Those patients who lived quite far from the Dental School were contacted by telephone. The patients were followed up for a year with the purpose of evaluating the recurrence rate after combination treatment with pine cone lignin and ascorbic acid. Photographs of the lesions were taken (not shown). Due to the difficulty of detecting HSV-1 patients, their previous clinical history and treatment experience were used as the control. The studied variables were: age, gender, physical findings, history of recurrent episodes, duration of the lesions, family cases, prodromal symptoms (burning, itching, pain, tingling sensation, sore throat and general malaise), reactivation stimuli (fever, sun exposure, trauma, physical or emotional stress, food allergy, respiratory tract infections and gastrointestinal diseases), location of the lesions (lips, and skin around the mouth and oral mucosa), number of lesions, evolution, reduction of symptoms and treatment previously used.

Interview procedure. Previous explanations of the nature of the study were given to the control group. Students and outclinic patients were asked if they had ever suffered ulcerations in the mouth with the following characteristics: ulceration in mobile mucosa with gum inflammation during early childhood, presence of ulcerations in lip skin or face, recurrence episodes associated with triggers. The subjects slides and clinical photographs of lesions in different stages of HSV-1 were also shown to them.

Patients and/or their companions were interviewed in the waiting rooms of clinics of the School of Dentistry of the Universidad Autonoma del Estrado de Mexico, while the students of the School of Dentistry were interviewed in their classrooms. Patients were interviewed about 35 semi-structured survey items in the dental office of the Oral Pathology Laboratory. The clinical review was conducted by using dental mirror and the established protection barriers.

Preparation of lignin-ascorbic acid tablets. The pine cone lignin fraction was prepared by a modification of the method previously reported (18). In brief, the cones of Pinus densiflora Sieb. et. Zucc. (obtained in Ehime, Japan) were washed with hot water and the residue was extracted with 1% NaOH. The NaOH extract was neutralized with hydrochloric acid, concentrated under reduced pressure and treated with ethanol. After centrifugation, the precipitate was dissolved in hot water to remove the ethanol, concentrated, mixed with dextrin and then finally dried to obtain the crude lignin fraction (pine cone extract powder JS) at an approximate yield of 50%.

Each lignin-ascorbic acid tablet contained a mixture of 50 mg pine cone extract powder JS, 50 mg ascorbic acid (BASF, Tokyo, Japan), 83 mg maltitol (Mitsubishi Shoji Foodtech Co., Ltd., Tokyo, Japan), 13 mg potato starch (Shirokuma Hokkai Food Co., Ltd., Sapporo, Japan) and 13 mg calcium stearate (Shinagawa Chemical Industry Co., Ltd, Tokyo, Japan).

Treatment schedule. The patients were administered one tablet of one mg before each meal daily for one month, or one mg of powder (tip of a coffee spoon), dissolved in a glass of boiled water or juice, before each meal daily also for one month. In the patients with recurrent onset, the treatment was repeated.

Statistical analysis. SPSS version 10.0 (Copyright© SPSS Inc., Chicago, USA) was used to analyze the association between variables by means of Chi-square Student's t-test and Kendall correlation. Differences were considered significant at p≤0.05.

Results

HSV-1-infected patients. In total, 48 HSV-1 patients were enrolled between January 2006 and December 2006; these patients were followed until December 2007. The female to male ratio was 1.82, most of the patients were in the first three decades of life, 29% were more than 40 years old (Figure 1).

Figure 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 1.

Distribution by age of HSV-1-infected patients studied according to gender.

Twenty-three percent of the total (11 patients out of 48 patients) started HSV-1 outbreaks in the first decade of life, 48% (23 patients) in the second decade and 29% (14 patients) after 21 years of age (Figure 2). Of them six patients, relatives of patients under study, developed HSV-1 infection for the first time, four were children and two adolescent, only one of them showed the typical features of primary herpetic gingivoestomatitis. There were significantly more patients (65%) who had affected relatives living at the same house, than those who had unaffected relatives (35%) (p=0.014 Chi-square test).

According to the patients' information, episode frequency varied from one recurrence episode to more than seven episodes per year (Figure 3).

All of the patients reported a combination of internal and external triggers of viral reactivation, as follows: fever (31%, 15 patients out of 48 patients), respiratory diseases (52%, 25 patients), gastrointestinal disorders (4%, 2 patients), emotional stress (48%, 23 patients), menstruation (6%, 3 patients), allergy (15%, 7 patients) and sun exposure (65%, 31 patients). Common prodromal symptoms were: tingling (15%, 7 patients), burning (15%, 7 patients), swelling (15%, 7 patients), itching (17%, 8 patients) and a combination of them including sore throat and malaise (40%, 19 patients). The skin of the lips was involved in 81% of the patients (39 patients), and the vermillion border in 19% (9 patients). A single lesion was observed in 31% (15 patients) of the patients with clinical evidence of lesion, while multiple lesions were noted in 36% (17 patients). The clinical manifestations are shown in Table II and were similar to those previously reported (1-4, 9). The mean size of the lesions was 0.938±0.483 cm (SD).

Figure 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 2.

Distribution by age at first outbreak among HSV-1-infected patients according to gender.

Figure 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 3.

History of episodes per year. N=42 patients. Six patients reported a first outbreak.

Anti-HSV-1 activity of lignin ascorbic acid combination treatment. The mean duration of the lesions in the patients who were treated with pine cone lignin and ascorbic acid in the first two days was significantly shorter (4.2±3.7 days) than that of the patients treated three to twelve days (8.3±4.9 days) (Figure 4). Fifty percent (24 patients) of the patients reported previous use of topical acyclovir, but 33% of them (8 out of the 24 patients) reported no reduction of the symptoms with that treatment or reduction in the recurrence episodes.

The pine cone lignin and ascorbic combination was administered to 58% (28 out of the 48 patients) in the first 48 hours of onset, to 21% (10 patients) between 48 and 72 hours and to 21% (10 patients) after 72 hours. In 81% (39 patients) of the cases, the symptoms decreased; the extent of the decrease depended on the day that the lignin-ascorbic acid combination treatment was started (Figure 5). Also 90% (43 patients) reported a reduction in the recurrence rate.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table II.

Clinical features of HSV lesions.

Only five patients presented a recurrence episode during the study (Figure 6). In four of these patients, there was a reduction in the frequency of the usual recurrence episodes; in one patient, the usual recurrence rate (1/year) did not change. In all five patients, the duration of the onsets was shorter than usual.

Discussion

The present study demonstrated that HSV-1 patients who took the pine cone lignin and ascorbic acid combination treatment in the first 48 hours after onset clearly manifested the efficacy of this treatment in reducing the length of the outbreak and reducing the symptoms. Even the patients who took the treatment on the subsequent days reported a beneficial effect, in comparison with their previous experience. It is possible that the treatment could benefit these latter patients to a small extent by accelerating healing. It seems that the inhibitory effect of pine cone lignin and ascorbic acid combination treatment on HVS-1 infection might depend on the antioxidant and immunopotentiating activities of lignin and ascorbic acid (18). The free radical scavenging activity of lignin (21) could attenuate oxidative stress and consequently induce antiviral protection. Although it has been reported that the use of herbal medicines can lead to severe adverse effects (22, 23), no patients in the present study presented any side-effects.

Figure 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 4.

Duration of lesions previous versus current treatment. Usual duration is based on patients' reports. Student's t-test, p=0.001.

Figure 5.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 5.

Symptoms reduction according to the day after onset, of starting pine cone lignin and ascorbic acid complex treatment. Symptoms were reduced significantly when the treatment was taken in the first 48 h; Kendall's Tau-b, p=0.001.

Figure 6.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 6.

Recurrence after the pine cone lignin-ascorbic acid complex treatment. N=48 patients.

A number of alternative medicines and dietary modifications have been administered with reproducible or conflicting results. The use of topical zinc for facial and circumoral herpes infection has been recommended, though zinc oxide can cause adverse effects (24, 25). The topical use of Melaleuca alternifolia (tea tree oil) reduced the time of re-epithelialization (26); also the dried leaf extract of lemon balm (Melissa officinalis), when administered locally, promoted the healing process and reduced the recurrence frequency (27). Ascorbic acid has been suggested to be useful for prevention of HSV-1 reactivation (28), and according to Terezhalmy et al. (29), 600 mg of water-soluble bioflavonoid and 600 mg of ascorbic acid reduced the bladder stage of HSV-1 and prevented the disruption of the vesicular membrane. Essential oils of ginger, thyme hyssop and sandalwood inactivated HSV before it entered cells, even in acyclovir-resistant HSV-1 (30). Propolis inhibited the viral entry in vitro (31) and interfered with the viral replication cycle in vivo (32).

In general, all studies agree that the chances of treatment success are correlated with lesion age, the first 24 to 48 hours being the most effective. This is the time during which the viral replication temporarily dominates the host immune response (8) and the response diminishes considerably with older lesions. The optimum treatment period is very brief, so to increase the chances of success, medication should be prospectively dispensed and treatment self-initiated by the patient at the first indication of a new episode (7). Patients in this study who received the treatment in the first 24 hours did not develop the typical symptoms of the onset; even those patients whose treatment was administrated within 72 hours reported a shorter duration of the episode.

The clinical aspects reported by the patients were similar to those reported in developing countries (11). The majority of the patients were in the third decade of life, the prevalence was low in children and adolescents. Twenty-nine percent of the patients were between forty and sixty years old, although it has been reported that the frequency of reactivation appears to decline after 35 years of age (33). These observations could be explained as 27% of the patients were students of the Dental School and the rest were patients or individuals accompanying patients to the Dentistry School's clinics. The prevalence of HSV is associated with low socioeconomic status (9), which is a common situation among patients who attend the Dentistry School's clinics.

Most cases of primary herpetic gingivostomatitis are subclinical, therefore children and adolescents, reporting a first outbreak in this study could be examples of previously undiagnosed primary episodes as they presented clinical manifestations of a recurrent onset rather than those described in primary herpetic gingivostomatitis (13).

The identification of familial cases living at the same house is not surprising since HSV infection could be spread via respiratory droplets or direct exposure to infected saliva (34). In addition to this internal trigger of HSV outbreak, external triggers, such as sun exposure, for possible enhanced HSV outbreak have been described previously (20, 30).

Although there were significant differences between the previous and current duration after the pine cone lignin and ascorbic acid combination treatment and differences in the reduction of symptoms taking into account historical data provided by the patients, the small number of patients and the lack of a control group limited our ability to generalize the results to a larger population. To evaluate the effectiveness of pine cone lignin and ascorbic acid combination treatment, subsequent randomized placebo-controlled studies must be conducted in a representative sample of the pediatric population to treat herpetic gingivostomatitis as well as in adults who suffer from recurrent HSV-1.

In conclusion, pine cone lignin and ascorbic acid combination has a potent antiviral activity, promoting faster healing, reduction of symptoms and reducing the frequency of recurrence episodes in HSV-1. Pine cone lignin and ascorbic acid combination could be useful in preventing and treating HSV infection.

Acknowledgements

This study was supported in part by Universidad Autonoma del Estado de Mexico (Gonzalez, FE04/2009) and a Grant-in-Aid from the Ministry of Education, Science, Sports and Culture of Japan (Sakagami, No. 19592156).

  • Received March 3, 2009.
  • Revision received August 14, 2009.
  • Accepted September 21, 2009.
  • Copyright © 2009 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved

References

  1. ↵
    1. Fatahzadeh M,
    2. Schwarts RA
    : Human herpes simplex labialis. Clin Exp Dermatol 32: 625-630, 2007.
    OpenUrlCrossRefPubMed
  2. ↵
    1. Whitley RJ,
    2. Roizman B
    : Herpes virus infections. Lancet 357: 1513-1518, 2001.
    OpenUrlCrossRefPubMed
  3. ↵
    1. Sciubba JJ
    : Herpes simplex and aphthous ulcerations. Presentation, diagnosis and management — an update. Gen Dent 51: 510-516, 2003.
    OpenUrlPubMed
  4. ↵
    1. Spruance SL,
    2. Wenerstrom GRN
    : Pathogenesis of recurrent herpes simplex labialis. IV Maturation of lesions within 8 hours after onset and implications for antiviral treatment. Oral Surg 58: 667-671, 1984.
    OpenUrlCrossRefPubMed
  5. ↵
    1. Rooney JF,
    2. Straus SE,
    3. Mannix ML,
    4. Wholenberg CR,
    5. Alling DW,
    6. Dumois JA,
    7. Notkins AL
    : Oral acyclovir to suppress frequently recurrent herpes labialis. A double-blind placebo-controlled trial. Ann Intern Med 118: 268-272, 1993.
    OpenUrlCrossRefPubMed
  6. ↵
    1. Balfour HH
    : Antiviral drugs. N Eng J Med 340: 1255-1268, 1999.
    OpenUrlCrossRefPubMed
  7. ↵
    1. Spruance SL,
    2. Nett R,
    3. Mabury T,
    4. Wolff R,
    5. Johnson J,
    6. Spaulding T,
    7. for the Acyclovir Cream Study Group
    : Acyclovir cream for treatment of herpes simplex labialis: results of two randomized, double bind, vehicle-controlled, multicenter clinical trials. Antimicrob Agents and Chemother 46: 2238-2243, 2002.
    OpenUrlAbstract/FREE Full Text
  8. ↵
    1. Spruance SL,
    2. Jones TM,
    3. Blatter MM,
    4. Vargas-Cortes M,
    5. Barber J,
    6. Hill J,
    7. Goldstein D,
    8. Schultz M,
    9. Valacyclovir Cold Sore Study Group
    : High-dose, short-duration early valaciclovir therapy for episodic treatment of cold sores: results of two randomized, placebo-controlled multicenter studies. Antimicrob Agents Chemother 47: 1072-1080, 2003.
    OpenUrlAbstract/FREE Full Text
  9. ↵
    1. Esmann J
    : The many challenges of facial herpes simplex virus infection. J Antimicrob Chemoter 47: 17-27, 2001.
    OpenUrlAbstract
  10. ↵
    1. Emmert DH
    : Treatment of common cutaneous herpes simplex virus infections. Am Fam Physician 61: 1697-1708, 2000.
    OpenUrlPubMed
  11. ↵
    1. Shaw M,
    2. King M,
    3. Best JM,
    4. Banatvala JE,
    5. Gibson JR,
    6. Klaber MR
    : Failure on acyclovir cream in treatment of recurrent herpes labialis. Brit Med J 291: 7-9, 1985.
    OpenUrlAbstract/FREE Full Text
  12. ↵
    1. Amir J,
    2. Harel L,
    3. Smetana Z,
    4. Varsano I
    : Treatment of herpes simplex gingivostomatitis with aciclovir in children: a randomised double blind placebo-controlled study. BMJ 314: 1800-1803, 1997.
    OpenUrlAbstract/FREE Full Text
  13. ↵
    1. Siegel MA
    : Diagnosis and management of recurrent herpes simplex infections. J Am Dent Assoc 133: 1245-1249, 2002.
    OpenUrlAbstract/FREE Full Text
  14. ↵
    1. Spruance SL
    : Prophylactic chemotherapy with acyclovir for recurrent herpes simplex labialis. J Med Virol 41: 27-32, 1993.
    OpenUrl
  15. ↵
    1. Alan GR
    : Natural remedies for herpes simplex (Herpes simplex). Altern Med Rev 11: 93-101, 2006.
    OpenUrlPubMed
  16. ↵
    1. Spruance SL,
    2. Freeman DJ,
    3. Stewart JC,
    4. McKeough MB,
    5. Wenerstrom LG,
    6. Krueger GG,
    7. Piepkorn MW,
    8. Stroop WG,
    9. Rowe NH
    : The natural history of ultraviolet radiation-induced herpes simplex labialis and response to therapy with peroral and topical formulations of acyclovir. J Infect Dis 163: 728-734, 1991.
    OpenUrlAbstract/FREE Full Text
  17. ↵
    1. Hamuy R,
    2. Berman B
    : Treatment of herpes simplex virus infections with topical antiviral agents. Eur J Dermatol 8: 310-319, 1998.
    OpenUrlPubMed
  18. ↵
    1. Sakagami H,
    2. Hashimoto K,
    3. Suzuki F,
    4. Ogiwara T,
    5. Satoh K,
    6. Ito H,
    7. Hatano T,
    8. Yoshida T,
    9. Fujisawa S
    : Molecular requirements of lignin-carbohydrate complexes for expression of unique biological activities. Phytochemistry 66: 2108-2120, 2005.
    OpenUrlPubMed
  19. ↵
    1. Sakagami H,
    2. Satoh K,
    3. Hakeda Y,
    4. Kumegawa M
    : Apoptosis-inducing activity of vitamin C and vitamin K. Cell Mol Biol 46: 129-143, 2000.
    OpenUrlPubMed
  20. ↵
    1. Paterson J,
    2. Kwong M
    : Recurrent herpes labialis. Assessment and non-prescription treatment. GlaxoSmithKline Continuing Education in Pharmacy CCCEP#268-0405 1-21, 2005 available in www.pharmacyresource.ca/recurrent_herpes_labialis.pdf (Consulted April 30, 2008).
  21. ↵
    1. Lu FJ,
    2. Chu LH,
    3. Gau RJ
    : Free radical-scavenging properties of lignin. Nutr Cancer 30: 31-38, 1998.
    OpenUrlPubMed
  22. ↵
    1. Bedi MK,
    2. Shenefelt PD
    : Herbal therapy in dermatology. Arch Dermatol 138: 232-242, 2002.
    OpenUrlCrossRefPubMed
  23. ↵
    1. Vender RB
    : Adverse reactions to herbal therapy in dermatology. Skin Ther Lett: 8:5-8, 2003. available in, http://www.skintherapyletter.com/2003/8.3/2.html (Consulted February 20, 2008).
    OpenUrl
  24. ↵
    1. Femiano F,
    2. Gombos F,
    3. Scully C
    : Recurrent herpes labialis: a pilot study of the efficacy of zinc therapy. J Oral Pathol Med 34: 423-425, 2005.
    OpenUrlPubMed
  25. ↵
    1. Godfrey HR,
    2. Godfrey NJ,
    3. Godfrey JC,
    4. Riley D
    : A randomized clinical trial on the treatment of oral herpes with topical zinc oxide/glycine. Altern Ther Health Med 7: 49-56, 2001.
    OpenUrlPubMed
  26. ↵
    1. Carson CF,
    2. Hammer KA,
    3. Riley TV
    : Melaleuca alternifolia (Tea tree) oil: a review on antimicrobial and other medicinal properties. Clin Microbiol Rev 19: 50-62, 2006.
    OpenUrlAbstract/FREE Full Text
  27. ↵
    1. Hoppe J
    : Melissa: Lemon balm as a topical treatment for herpes simplex virus. Med Herbalism 11: 13-16, 1999.
    OpenUrl
  28. ↵
    1. Yoon JC,
    2. Cho JJ,
    3. Yoo SM,
    4. Ha YM
    : Antiviral activity of ascorbic acid against herpes simplex virus. J Korean Soc Microbiol 35: 1-8, 2000.
    OpenUrl
  29. ↵
    1. Terezhalmy GT,
    2. Bottomley WK,
    3. Pelleu GB
    : The use of water-soluble bioflavonoid ascorbic acid complex in the treatment of recurrent herpes labialis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 45: 56-62, 1978.
    OpenUrl
  30. ↵
    1. Schnitzler P,
    2. Koch C,
    3. Reichling J
    : Susceptibility of drug—resistant clinical herpes simplex virus type 1 strains to essential oils of ginger, thyme, hyssop, and sandalwood. Antimicrob Agents Chemother 51: 1859-1862, 2007.
    OpenUrlAbstract/FREE Full Text
  31. ↵
    1. Gekker G,
    2. Hu S,
    3. Spivak M,
    4. Lokensgard JR,
    5. Peterson FK
    : Anti-HIV-1 activity of propolis in CD4+ lymphocyte and microglial cell cultures. J Ethnopharmacol 102: 158-163, 2005.
    OpenUrlPubMed
  32. ↵
    1. Huleihel M,
    2. Isanu V
    : Anti-herpes simplex virus effect of an aqueous extract of propolis. IMAJ 4(Suppl): 923-927, 2002.
    OpenUrlPubMed
  33. ↵
    1. Spruance SL,
    2. Overall JC,
    3. Kern ER,
    4. Krueger GG,
    5. Pliam V,
    6. Miller W
    : The natural history of recurrent herpes simplex labialis; implications for antiviral therapy. N Eng J Med 297: 69-75, 1977.
    OpenUrlCrossRefPubMed
  34. ↵
    1. Corey L,
    2. Spear PG
    : Infections with herpes simplex viruses. N Eng J Med 314: 686-691 1986.
    OpenUrlCrossRefPubMed
PreviousNext
Back to top

In this issue

In Vivo
Vol. 23, Issue 6
November-December 2009
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Back Matter (PDF)
  • Front Matter (PDF)
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on In Vivo.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
A Clinical Pilot Study of Lignin—Ascorbic Acid Combination Treatment of Herpes Simplex Virus
(Your Name) has sent you a message from In Vivo
(Your Name) thought you would like to see the In Vivo web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
7 + 0 =
Solve this simple math problem and enter the result. E.g. for 1+3, enter 4.
Citation Tools
A Clinical Pilot Study of Lignin—Ascorbic Acid Combination Treatment of Herpes Simplex Virus
BLANCA SILVIA GONZALEZ LOPEZ, MASAJI YAMAMOTO, KATSUAKI UTSUMI, CHIAKI ARATSU, HIROSHI SAKAGAMI
In Vivo Nov 2009, 23 (6) 1011-1016;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Reprints and Permissions
Share
A Clinical Pilot Study of Lignin—Ascorbic Acid Combination Treatment of Herpes Simplex Virus
BLANCA SILVIA GONZALEZ LOPEZ, MASAJI YAMAMOTO, KATSUAKI UTSUMI, CHIAKI ARATSU, HIROSHI SAKAGAMI
In Vivo Nov 2009, 23 (6) 1011-1016;
Reddit logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Patients and Methods
    • Results
    • Discussion
    • Acknowledgements
    • References
  • Figures & Data
  • Info & Metrics
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • Prominent Anti-UV Activity and Possible Cosmetic Potential of Lignin-carbohydrate Complex
  • Synergism of Alkaline Extract of the Leaves of Sasa senanensis Rehder and Antiviral Agents
  • Anti-Halitosis Effect of Toothpaste Supplemented with Alkaline Extract of the Leaves of Sasa senanensis Rehder
  • Efficient Utilization of Licorice Root by Alkaline Extraction
  • Biological Interaction between Sasa senanensis Rehder Leaf Extract and Toothpaste Ingredients
  • Structural Characterization of Anti-UV Components from Sasa senanensis Rehder Extract
  • Pilot Clinical Study of Sasa senanensis Rehder Leaf Extract Treatment on Lichenoid Dysplasia
  • Google Scholar

More in this TOC Section

  • Response to Letter to the Editor from Finsterer: “Encephalitis Associated With SARS-CoV-2 Infection in a Child With Chiari Malformation Type I”
  • Solitary Fibrous Tumor in the Retroperitoneal Space Arising from the Diaphragm
  • The Relationship Between Oxidative Stress, Selenium, and Cumulative Risk in Metabolic Syndrome
Show more Clinical Studies

Similar Articles

In Vivo

© 2023 In Vivo

Powered by HighWire