The DOI matches its Crossref record.
Acute Anisakiasis: Pharmacological Evaluation of Various Drugs in an Animal Model
Abstract
Background The accidental ingestion of the third larval stage of Anisakis can cause acute clinical symptoms, which are relieved via extraction of the larvae. Although this is a highly effective technique, it can only be practiced when the larvae are found in accessible areas of the gastrointestinal tract, and therefore instead the condition has often been treated using various different drugs. Aims This study evaluates the effectiveness of gastric acid secretion inhibitors (omeprazole and ranitidine), gastric mucosal protectants (sucralfate) and anthelmintics (mebendazole and flubendazole) in treating anisakiasis in Wistar rats. Methods Rats were infected with Anisakis-type I larvae and administered the drugs via a gastric probe. Data were recorded regarding the number of live and dead larvae, their location both within the animal and in its feces, and the presence of gastrointestinal lesions. Additionally, gastric pH was measured and histology performed. Results While rats in all experimental groups exhibited lesions; those treated with ranitidine and mebendazole showed significantly fewer lesions (50% and 35% of rats exhibited lesions, respectively). Histological examination of the gastric lesions revealed infection-induced changes, but no significant differences were observed between the treated and untreated rats. Conclusions Mebendazole was found to be most efficacious in preventing gastrointestinal lesions, followed by ranitidine, which was the most effective antacid of those studied. Both these drugs could thus be considered as part of the conservative management of anisakiasis.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Of considerable interest to note is that mebendazole was recently highlighted to be a more effective drug than albendazole and flubendazole in reducing lesion occurrence in experimentally infected rats [94].”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [94]
Citations
Cites
Still being checked.
Research works printed but not linked: 56
- Smith JW, Wootten R. Anisakis and anisakiasis. Adv Parasitol. 1978;16:93–163. · DOI
- Chía N, Romero MC, Polo-Vico R, Gómez-Mateos M, Abattouy N, Valero A. Epidemiological study of Anisakis type I in blue whiting (Micromesistius poutassou) captured in northwestern Spain. Ars Pharm. 2010;51:829–834.
- Molina-Fernández D, Malagón D, Gómez-Mateos M, Benítez R, Martín-Sánchez J, Adroher FJ. Fishing area and fish size as risk factors of Anisakis infection in sardines (Sardina pilchardus) from Iberian waters, southwestern Europe. Int J Food Microbiol. 2015;203:27–34. · DOI
- Levsen A, Cipriani P, Mattiucci S, et al. Anisakis species composition and infection characteristics in Atlantic mackerel, Scomber scombrus, from major European fishing grounds—reflecting changing fish host distribution and migration pattern. Fish Res. 2017;202:112–121. · DOI
- Van Thiel P. Larva migrans visceralis. Ned Tijdschr Geneeskd. 1960;104:1104–1107.
- Chai JY, Darwin Murrell K, Lymbery AJ. Fish-borne parasitic zoonoses: status and issues. Int J Parasitol. 2005;35:1233–5124. · DOI
- Mattiucci S, Paoletti M, Borrini F, et al. First molecular identification of the zoonotic parasite Anisakis pegreffii (Nematoda: Anisakidae) in a paraffin-embedded granuloma taken from a case of human intestinal anisakiasis in Italy. BMC Infect Dis. 2011;11:82. · DOI
- Li SW, Shiao SH, Weng SC, Liu TH, Su KE, Chen CC. A case of human infection with Anisakis simplex in Taiwan. Gastrointest Endosc. 2015;82:757–758. · DOI
- Lim H, Jung B, Cho J, Yooyen T, Shin E, Chai J. Molecular diagnosis of cause of anisakiasis, South Korea. Emerg Infect Dis. 2015;21:342–344. · DOI
- Amir A, Ngui R, Lau YL, et al. Anisakiasis causing acute dysentery in Malaysia. Am J Trop Med Hyg. 2016;95:410–412. · DOI
- Moneo I, Carballeda-Sangiao N, González-Muñoz M. New perspectives on the diagnosis of allergy to Anisakis spp. Curr Allergy Asthma Rep. 2017;17:27. · DOI
- Bouwknegt M, Devleesschauwer B, Graham H, Robertson LJ, Van der Giessen JW. The Euro-Fbp workshop participants. Prioritisation of food-borne parasites in Europe, 2016. Euro Surveill. 2018. https://doi.org/10.2807/1560-7917.ES.2018.23.9.17-00161. · DOI
- Bao M, Pierce GJ, Pascual S, et al. Assessing the risk of an emerging zoonosis of worldwide concern: anisakiasis. Sci Rep. 2017;7:43699. · DOI
- Herrador Z, Daschner Á, Perteguer MJ, Benito A. Epidemiological scenario of anisakidosis in Spain based on associated hospitalizations: the tipping point of the iceberg. Clin Infect Dis. 2019;69:69–76. · DOI
- Audicana MT, Kennedy MW. Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin Microbiol Rev. 2008;21:360–379. · DOI
- Morsy K, Badr AM, Abdel-Ghaffar F, El Deeb S, Ebead S. Pathogenic potential of fresh, frozen, and thermally treated Anisakis spp. type II (L3) (Nematoda: Anisakidae) after oral inoculation into wistar rats: a histopathological study. J Nematol. 2017;49:427–436. · DOI
- Shimamura Y, Muwanwella N, Chandran S, Kandel G, Marcon N. Common symptoms from an uncommon infection: gastrointestinal anisakiasis. Can J Gastroenterol Hepatol. 2016;2016:5176502. · DOI
- Shibata E, Ueda T, Akaike G, Saida Y. CT findings of gastric and intestinal anisakiasis. Abdom Imaging. 2014;39:257–261. · DOI
- Takabayashi T, Mochizuki T, Otani N, Nishiyama K, Ishimatsu S. Anisakiasis presenting to the ED: clinical manifestations, time course, hematologic tests, computed tomographic findings, and treatment. Am J Emerg Med. 2014;32:1485–1489. · DOI
- Fuchizaki U, Nishikawa M. Images in clinical medicine. Gastric Anisakiasis. N Engl J Med. 2016;375:e11. · DOI
- Baron L, Branca G, Trombetta C, et al. Intestinal anisakidosis: histopathological findings and differential diagnosis. Pathol Res Pract. 2014;210:746–750. · DOI
- Theodore E. Anisakiasis. In: Gerald L, John E, Raphael D, eds. Principles and Practice of Infectious Diseases. Philadelphia: Elsevier Churchill Livingstone; 2005:3295.
- De la Fuente E, Agudo S, Blasco S, Cacho G, Fernández C. Casos clínicos: caso de anisakiasis gastroalérgica documentado endoscópicamente. Rev Esp Enferm Dig. 2013;105:245–380. · DOI
- Nakata H, Takeda K, Nakayama T. Radiological diagnosis of acute gastric anisakiasis. Radiology. 1980;135:49–53. · DOI
- Cocheton JJ, Cabou I, Lecomte I. Anisakiasis and Anisakis infections. Ann Med Interne. 1991;142:121–130.
- Iglesias L, Valero A, Benítez R, Adroher FJ. In vitro cultivation of Anisakis simplex: pepsin increases survival and moulting from fourth larval to adult stage. Parasitology. 2001;123:285–291. · DOI
- Henríquez-Santana A, Villafruela-Cives M. Anisakis: past, present and future. Med Clin. 2009;132:400–403. · DOI
- Moore D, Girdwood R, Chiodini P. Treatment of anisakiasis with albendazole. Lancet. 2002;360:54. · DOI
- Kim T, Lee B, Sohn W. Three clinical cases of cutaneous larva migrans. Korean J Parasitol. 2006;44:145–149. · DOI
- Kim SH, Park CW, Kim SK, et al. A case of anisakiasis invading the stomach and the colon at the same time after eating anchovies. Clin Endosc. 2013;46:293–296. · DOI
- 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. · DOI
- Arias-Diaz J, Zuloaga J, Vara E, Balibrea J, Balibrea JL. Efficacy of albendazole against Anisakis simplex larvae in vitro. Dig Liver Dis. 2006;38:24–26. · DOI
- Lin RJ, Chen CY, Lee JD, Lu CM, Chung LY, Yen CM. Larvicidal constituents of Zingiber officinale (Ginger) against Anisakis simplex. Planta Med. 2010;76:1852–1858. · DOI
- Lopieńska-Biernat E, Molcan T, Paukszto L, Jastrzębski JP, Myszczyński K. Modelling studies determing the mode of action of anthelmintics inhibiting in vitro trehalose-6-phosphate phosphatase (TPP) of Anisakis simplex s.l. Exp Parasitol. 2018;184:46–56. · DOI
- Mladineo I, Trumbić Ž, Hrabar J, et al. Efficiency of target larvicides is conditioned by ABC-mediated transport in the zoonotic nematode Anisakis pegreffii. Antimicrob Agents Chemother. 2018;62:1–14. · DOI
- Hierro I, Valero A, Pérez P, et al. Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae. Phytomedicine. 2004;11:77–82. · DOI
- Navarro MC, Noguera MA, Romero MC, Montilla MP, González de Selgas JM, Valero A. Anisakis simplex s.l.: larvicidal activity of various monoterpenic derivatives of natural origin against L3 larvae in vitro and in vivo. Exp Parasitol. 2008;120:295–299. · DOI
- Romero MC, Navarro MC, Martín-Sánchez J, Valero A. Peppermint (Mentha piperita) and albendazole against anisakiasis in an animal model. Trop Med Int Health. 2014;19:1430–1436. · DOI
- Quiñones-Silva J, Sánchez-Aldehuelo R, Solorzano C, Zamorano M, Parejo-Carbonell S. Anisakiasis como diagnóstico diferencial de dolor abdominal agudo en urgencias. Rev Gastroenterol Peru. 2019;39:171–174. (Spanish).
- Field-Cortazares J, Calderón-Campos R. Intoxicación por Anisakis. Bol Clin Hosp Infant Edo Son. 2009;26:43–47.
- Fraj-Lázaro J, Remacha-Tomey B, Colás-Sanz C, Ortega-Fernández de Retana A, Lezaun-Alfonso A. Anisakis, anisakiasis and IgE-mediated immunity to Anisakis simplex. J Investig Allergol Clin Immunol. 1998;8:61–63.
- Castán B, Borda F, Iñarrairaegui M, Pastor G, Vila J, Zozaya JM. Digestive anisakiasis: clinical manifestations and diagnosis according to localization. Rev Esp Enferm Dig. 2002;94:463–742.
- Pinto LC, Mesquita FP, Soares BM, et al. Mebendazole induces apoptosis via C-MYC inactivation in malignant ascites cell line (AGP01). Toxicol Vitr. 2019;60:305–312. · DOI
- Nawa Y, Hatz C, Blum J. Sushi delights and parasites: the risk of fishborne and foodborne parasitic zoonoses in Asia. Clin Infect Dis. 2005;41:1297–1303. · DOI
- Pacios E, Arias-Díaz J, Zuloaga J, Gonzalez-Armengol J, Villarroel P, Balibrea JL. Albendazole for the treatment of anisakiasis ileus. Clin Infect Dis. 2005;41:1825–1826. · DOI
- Filauro M, Rollandi GA, Cassola G, et al. Gastrointestinal bleeding due to suspected anisakiasis: challenging differential diagnosis for a rare disease. Updat Surg. 2011;63:213–217. · DOI
- Pontone S, Leonetti G, Guaitoli E, et al. Should the host reaction to anisakiasis influence the treatment? Different clinical presentations in two cases. Rev Esp Enferm Dig. 2012;104:607–610. · DOI
- Baptista-Fernandes T, Rodrigues M, Castro I, et al. Human gastric hyperinfection by Anisakis simplex: a severe and unusual presentation and a brief review. Int J Infect Dis. 2017;64:38–41. · DOI
- Romero MC, Valero A, Navarro MC, Hierro I, Barón SD, Martín-Sánchez J. Experimental demonstration of pathogenic potential of Anisakis physeteris and Anisakis paggiae in Wistar rats. Parasitol Res. 2014;113:4377–4386. · DOI
- Del Pozo V, Arrieta I, Tuñon T, et al. Immunopathogenesis of human gastrointestinal infection by Anisakis simplex. J Allergy Clin Immunol. 1999;104:637–643. · DOI
- Bier JW, Raybourne RB. Anisakis simplex (Nematoda: Ascaridoides): formation of immunogenic attachment caps in pigs. Proc Helminthol Soc Wash. 1988;55:91–94.
- Iglesias R. La anisakiosis y su diagnóstico [Dissertation]. Santiago de Compostela: University of Santiago de Compostela; 1998.
- Bušelić I, Trumbić Ž, Hrabar J, Vrbatović A, Bočina I, Mladineo I. Molecular and cellular response to experimental Anisakis pegreffii (nematoda, anisakidae) third-stage larval infection in rats. Front Immunol. 2018;9:2055. · DOI
- Kang DB, Park WC, Lee JK. Chronic gastric anisakiasis provoking a bleeding gastric ulcer. Ann Surg Treat Res. 2014;86:270–273. · DOI
- Hollingworth S, Duncan E, Martin J. Marked increase in proton pump inhibitors use in Australia. Pharmacoepidemiol Drug Saf. 2010;19:1019–1024. · DOI
- Ministerio de Sanidad SS e I. Subgroups ATC and active ingredients of greater consumption in the National Health System in 2010. Inf Ter del Sist Nac Salud. 2011;35:124–128. (Spanish).
Cited by
Sorted by citations
Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update
Chai, J.-Y., Jung, B.-K., & Hong, S.-J. (2021) · The Korean Journal of Parasitology · doi:10.3347/kjp.2021.59.3.189 · Cited by 286
Metadata
- Authors
- Gómez-Mateos, M., Arrebola, F., Navarro, M. C., Romero, M. C., González, J. M., & Valero, A.
- Affiliations
- Universidad de Granada (ES)
- Venue
- Digestive Diseases and Sciences
- Published
- 2020-02-27
- Volume
- 66
- Issue
- 1
- Pages
- 105-113
- ISSN
- 0163-2116 (ISSN-L)
- 1573-2568
- OpenAlex
- W3007258297
- Cited by
- 6
- References
- 0
- Citations by year
- 2025: 1 · 2024: 1 · 2022: 1 · 2021: 3
- FWCI
- 0.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Digestive Diseases and Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía (BIO-243)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Parasitic Diseases Research and Treatment
- Life Sciences › Immunology and Microbiology › Parasitology › Parasitic infections in humans and animals
- Life Sciences › Immunology and Microbiology › Parasitology › Helminth infection and control
- Keywords
- anisakiasis, Anisakis, mebendazole, ranitidine, omeprazole, sucralfate, flubendazole, anthelmintics, gastric acid secretion inhibitors, gastrointestinal lesions, larval migration, conservative treatment
- MeSH terms
- Acute Disease, Animals, Anthelmintics, Anti-Ulcer Agents, Antinematodal Agents, Disease Models, Animal, Drug Evaluation, Preclinical, Female, Fishes, Mebendazole, Omeprazole, Ranitidine, Sucralfate, Anisakiasis, Rats, Wistar, Gastrointestinal Tract, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Acute Anisakiasis: Pharmacological Evaluation of Various Drugs in an Animal Model. https://app.cochat.ai/papers/10.1007/s10620-020-06144-2
- The paper
- Gómez-Mateos, M., Arrebola, F., Navarro, M. C., Romero, M. C., González, J. M., & Valero, A. (2021). Acute Anisakiasis: Pharmacological Evaluation of Various Drugs in an Animal Model. Digestive Diseases and Sciences. https://doi.org/10.1007/s10620-020-06144-2