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DOI: 10.1055/s-0030-1249971
© Georg Thieme Verlag KG Stuttgart · New York
Larvicidal Constituents of Zingiber officinale (Ginger) against Anisakis simplex
Publication History
received February 3, 2010
revised April 17, 2010
accepted April 23, 2010
Publication Date:
08 June 2010 (online)
Abstract
In this study, we investigated the anthelmintic activity of [10]-shogaol, [6]-shogaol, [10]-gingerol and [6]-gingerol, compounds isolated from the roots of Zingiber officinale L., Zingiberaceae (ginger), against Anisakis simplex. The above compounds kill or reduce spontaneous movement in A. simplex larvae. The maximum lethal efficacy of [10]-shogaol and [10]-gingerol was approximately 80 % and 100 %, respectively. We further examined the time course of compound-induced loss of mobility in A. simplex. The results showed that various concentrations of [10]-shogaol, [6]-shogaol, [10]-gingerol and [6]-gingerol have maximum effects on loss of spontaneous movement from 24 to 72 h. In addition, the time course of mortality and the percentage of loss of spontaneous movements were ascertained to determine the minimum effective doses of [10]-gingerol and [10]-shogaol. [10]-Gingerol exhibited a larger maximum larvicidal effect and greater loss of spontaneous movement than [10]-shogaol and albendazole. In addition, these constituents of Zingiber officinale showed effects against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and peroxyl radicals. These constituents of Zingiber officinale are responsible for its larvicidal activity against A. simplex.
Key words
Zingiber officinale L. - Zingiberaceae (ginger) - Anisakis simplex - larvicidal activity - anthelmintic activity
References
- 1 Goto C, Kasuya S, Koga K, Ohtomo H, Kagei N. Lethal efficacy of extract from Zingiber officinale (traditional Chinese medicine) or [6]-shogaol and [6]-gingerol in Anisakis larvae in vitro. Parasitol Res. 1990; 76 653-656
- 2 Chohan M, Forster-Wilkins G, Opara E I. Determination of the antioxidant capacity of culinary herbs subjected to various cooking and storage processes using the ABTS(*+) radical cation assay. Plant Foods Hum Nutr. 2008; 63 47-52
- 3 Ali B H, Blunden G, Tanira M O, Nemmar A. Some phytochemical, pharmacological and toxicological properties of ginger (Zingiber officinale Roscoe): a review of recent research. Food Chem Toxicol. 2008; 46 409-420
- 4 Langmead L, Rampton D S. Review article: herbal treatment in gastrointestinal and liver disease–benefits and dangers. Aliment Pharmacol Ther. 2001; 15 1239-1252
- 5 Park K K, Chun K S, Lee J M, Lee S S, Surh Y J. Inhibitory effects of [6]-gingerol, a major pungent principle of ginger, on phorbol ester-induced inflammation, epidermal ornithine decarboxylase activity and skin tumor promotion in ICR mice. Cancer Lett. 1998; 129 139-144
- 6 Iqbal Z, Lateef M, Akhtar M S, Ghayur M N, Gilani A H. In vivo anthelmintic activity of ginger against gastrointestinal nematodes of sheep. J Ethnopharmacol. 2006; 106 285-287
- 7 Sanderson L, Bartlett A, Whitfield P J. In vitro and in vivo studies on the bioactivity of a ginger (Zingiber officinale) extract towards adult schistosomes and their egg production. J Helminthol. 2002; 76 241-247
- 8 Craig W, Beck L. Phytochemicals: health protective effects. Can J Diet Pract Res. 1999; 60 78-84
- 9 Craig W J. Phytochemicals: guardians of our health. J Am Diet Assoc. 1997; 97 S199-S204
- 10 Courdurier J, Gillon J C, Malarde L. [Realization of the cycle of Angiostrongylus cantonensis (Chen) in the laboratory. 3. Chronic lesions of the lungs in rats experimentally infected]. Bull Soc Pathol Exot Filiales. 1968; 61 254-259
- 11 Guilhon J, Mishra G S, Barnabe R. [Effect of different nematodicides on Angiostrongylus cantonensis (Chen, 1935) at different periods of its development, in the rat]. C R Acad Sci Hebd Seances Acad Sci D. 1973; 676 857-860
- 12 Takei H, Powell S Z. Intestinal anisakidosis (anisakiosis). Ann Diagn Pathol. 2007; 11 350-352
- 13 Caramello P, Vitali A, Canta F, Caldana A, Santi F, Caputo A, Lipani F, Balbiano R. Intestinal localization of anisakiasis manifested as acute abdomen. Clin Microbiol Infect. 2003; 9 734-737
- 14 Deardorff T L, Kayes S G, Fukumura T. Human anisakiasis transmitted by marine food products. Hawaii Med J. 1991; 50 9-16
- 15 Schuster R, Petrini J L, Choi R. Anisakiasis of the colon presenting as bowel obstruction. Am Surg. 2003; 69 350-352
- 16 Arias-Diaz J, Zuloaga J, Vara E, Balibrea J, Balibrea J L. Efficacy of albendazole against Anisakis simplex larvae in vitro. Dig Liver Dis. 2006; 38 24-26
- 17 Adewunmi C O, Oguntimein B O, Furu P. Molluscicidal and antischistosomal activities of Zingiber officinale. Planta Med. 1990; 56 374-376
- 18 Datta A, Sukul N C. Antifilarial effect of Zingiber officinale on Dirofilaria immitis. J Helminthol. 1987; 61 268-270
- 19 Favier A. [Oxidative stress in human diseases]. Ann Pharm Fr. 2006; 64 390-396
- 20 Diallo D, Marston A, Terreaux C, Toure Y, Paulsen B S, Hostettmann K. Screening of Malian medicinal plants for antifungal, larvicidal, molluscicidal, antioxidant and radical scavenging activities. Phytother Res. 2001; 15 401-406
- 21 Lopes N P, Chicaro P, Kato M J, Albuquerque S, Yoshida M. Flavonoids and lignans from Virola surinamensis twigs and their in vitro activity against Trypanosoma cruzi. Planta Med. 1998; 64 667-668
- 22 Shoji N, Iwasa A, Takemoto T, Ishida Y, Ohizumi Y. Cardiotonic principles of ginger (Zingiber officinale Roscoe). J Pharm Sci. 1982; 71 1174-1175
- 23 Connel D W, Sutherland M D. A re-examination of gingerol, shogaol, and zingerone, the pungent principles of ginger (Zingiber officinale Roscoe). Aust J Chem. 1969; 22 1033-1043
- 24 Kikuzaki H, Usuguchi J, Nakatani N. Constituents of zingiberaceae. I. Diarylheptanoids from the rhizomes of ginger (Zingiber officinale Roscoe). Chem Pharm Bull. 1991; 39 120-122
- 25 Iglesias L, Valero A, Benitez R, Adroher F J. In vitro cultivation of Anisakis simplex: pepsin increases survival and moulting from fourth larval to adult stage. Parasitology. 2001; 123 285-291
- 26 Kiuchi F, Miyashita N, Tsuda Y, Kondo K, Yoshimura H. Studies on crude drugs effective on visceral larva migrans. I. Identification of larvicidal principles in betel nuts. Chem Pharm Bull. 1987; 35 2880-2886
- 27 Hwang B Y, Kim H S, Lee J H, Hong Y S, Ro J S, Lee K S, Lee J J. Antioxidant benzoylated flavan-3-ol glycoside from Celastrus orbiculatus. J Nat Prod. 2001; 64 82-84
- 28 Gillespie K M, Chae J M, Ainsworth E A. Rapid measurement of total antioxidant capacity in plants. Nat Protoc. 2007; 2 867-870
- 29 Dziekonska-Rynko J, Rokicki J, Jablonowski Z. Effects of ivermectin and albendazole against Anisakis simplex in vitro and in guinea pigs. J Parasitol. 2002; 88 395-398
- 30 Hierro I, Valero A, Perez P, Gonzalez P, Cabo M M, Montilla M P, Navarro M C. Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae. Phytomedicine. 2004; 11 77-82
Chuan-Min Yen
Department of Parasitology and Institute of Medicine
College of Medicine
Kaohsiung Medical University
100 shih-Chuan 1st Road
Kaohsiung, 80708
Taiwan
Republic of China
Phone: + 8 86 73 12 11 01 ext. 21 69
Fax: + 8 86 73 21 83 09
Email: chmiye@kmu.edu.tw