Pandey et al. UJP 2013, 02 (02): Page 1-3 www.ujponline.com Universal Journal of Pharmacy Review Article ISSN 2320-303X Take Research to New Heights TREATMENT FOR CERTAIN PARASITIC DISEASES OF FISHES Pandey Govind* * Professor/Principal Scientist & In-Charge, Department of Veterinary Pharmacology & Toxicology, College of Veterinary Science & Animal Husbandry, Rewa The Nanaji Deshmukh Veterinary Science University (NDVSU), Jabalpur, MP, India Received 26-02-2013; Revised 10-03-2013; Accepted 12-04-2013 ABSTRACT The parasitic infection may cause severe morbidity and mortality in fish. For example, the flagellates of the “Hexamita” parasite are often associated with high mortality in fish. The flagellate parasites interfere with nutrition by competing for essential nutrients and/or by damaging the intestinal epithelium. The ‘hexamitosis’ is probably the most frequent internal flagellate parasitosis of fish, notably in the young salmonids. The H. salmonis infected fish pass both trophozoites and cysts in faeces. Several drugs have been investigated for the treatment of parasite infection in different species of fish. However, the only oral pharmacological treatment of H. salmonis determined to date have been the drugs of nitroimidazole group, which show the activity against different protozoan groups, including flagellates and ciliates. The current treatment of choice is dimetridazole or metronidazole in the feed. The H. salmonis infection in the rainbow trout (Oncorhynchus mykiss) fish was completely eradicated not only by the metronidazole, but also by benznidazole, ronidazole and secnidazole. The four nitroimidazoles, e.g., albendazole, aminosidine, diethylcarbamazine and nitroscanate completely eliminated the parasite infection in the fish. Three drugs have been also been recommended for the treatment of protozoan parasitoses of fish, viz., amprolium, bithionol and toltrazuril. Among these three (amprolium, bithionol and toltrazuril), amprolium was found to be effective after oral administration; indeed, its administration by this route is recommended for myxosporidiosis. Bithionol and toltrazuril have been effective only in the bath treatments. Keywords: Disease, Antiparasitic Drugs, Fish, Parasites, Treatment. INTRODUCTION The intestinal infection of fish by many parasites can cause severe morbidity and mortality. For instance, the flagellates of the Hexamita parasite are often associated with high mortality in fish. Some workers have suggested that the pathological effects arise when the host is weakened by other factors like inadequate diet, change in diet, low oxygen content in the water, overcrowding, inappropriate handling and/or keeping fish of different sizes together1. It has been suggested that the flagellate parasites interfere with nutrition by competing for essential nutrients and/or by damaging the intestinal epithelium2. In both salmonids and tropical aquarium fish, the intestinal parasitoses are *Corresponding author: Dr. Govind Pandey Professor/Principal Scientist & In-Charge, Deptt. of Veterinary Pharmacology & Toxicology, College of Veterinary Science & AH, Rewa (NDVSU, Jabalpur), MP. E-mail: drgovindpandey@rediffmail.com often pathogenic only when the number of parasites present is very high3. The hexamitosis is probably the most frequent internal flagellate parasitosis of fish, notably in the young salmonids, though also in carp, aquarium species and various marine fish. Heavily infected fish are weak, listless, anorexic and emaciated, so that the head of a particular fish appears large with respect to the body (‘pinhead fish’). The affected fish typically swim on their side, or with corkscrew movements. Populations affected by the acute hexamitosis show high mortality over a very short period, due to rapid multiplication of the parasite and associated damage to the intestinal epithelium. The chronic form of hexamitosis is likewise common, and generally occurs between spring and autumn; mortality per unit time is only slightly higher than in healthy fish, but severe losses may occur because the situation continues for a period of weeks 4. In trout and other salmonid fish infected with Hexamita salmonis parasite, the adverse effects commonly observed are anaemia, weight loss5, dark coloration, enteritis, excessive body mucus and yellowish intestinal Universal Journal of Pharmacy, 02(02), Mar-Apr 2013 xx Pandey et al. UJP 2013, 02 (02): Page 1-3 mucus (attributable to modified release of bile into the digestive tract). In addition, the intestinal haemorrhage and liver cell necrosis may also be observed3. It is worth noting that the H. salmonis infected fish pass both trophozoites and cysts in faeces4. The fish that appear to be heavily infected (i.e., numerous parasites in the pyloric caecae and the intestine) may show no signs of damage to the mucosa, and no evidence of invasion of the epithelium by the parasite. Cysts were not observed at any stage, even after subjecting samples to concentration methods such as the Bailinger method. Cysts thus appear to be very rare6. Several drugs have been investigated for the treatment of parasite infection in different species of fish. However, the only oral pharmacological treatment of H. salmonis determined to date have been the drugs of nitroimidazole group7-8, which show the activity against different protozoan groups, including flagellates and ciliates. Therefore, the current treatment of choice is dimetridazole or metronidazole in the feed3-4,9. Further, there have been few studies of the possible anti-Hexamita or antiparasitic effect of the drugs of other groups. Treatment for ectoparasitic diseases in freshwater fish with formalin seems at present to be ineffective. Formalin possibly leaves toxic residues in fish flesh and in the environment which are eventually harmful to the consumers. The alternative way to solve this problem is to use traditional medicinal plants instead10. The treatment with medicinal plants having antibacterial activity is a potentially beneficial alternative in the aquaculture. These herbs mitigate many of the side effects which are associated with synthetic antimicrobials. Additionally, the plantderived phytomedicines provide a cheaper source for treatment and greater accuracy than chemotherapeutic agents. Recently, research has been initiated to evaluate the feasibility of herbal drugs in fish diseases11-12. In view of the above facts, the present article elucidates regarding some of the antiparasitic drugs which have been cited for the treatment of certain parasitic diseases of the fish. Some Antiparasitic Drugs against Fish Parasites: The results a study6 confirm the efficacy of nitroimidazoles against the parasitic diseases of fish. In this study, the H. salmonis infection in the rainbow trout (Oncorhynchus mykiss) fish was completely eradicated not only by the metronidazole (which has been recommended earlier for the treatment of hexamtosis), but also by benznidazole, ronidazole and secnidazole (which have not been assayed previously). The non-nitroimidazoles, e.g. albendazole, amnosidine, diethethylcarbamazine and nitroscanate also completely eliminated the infection. The remaining non-nitroimidazoles tested (amprolium, bithionol, febantel, flubendazole, levamisole, netobimin, www.ujponline.com niclosamide, nitroxynil, oxibendazole, parbendazole, piperazine, praziquentel, tetramisole, thiophanate, toltrazuril, trichlorfon and triclabendazole) were found not effective. The four nitroimidazoles (albendazole, aminosidine, diethylcarbamazine, nitroscanate) completely eliminated the infection @ 5 g/kg feed for 2 days 4. All nitroimidazoles except metronidazole were effective even at the lower dose of 2 g/kg feed for 2 days. These results confirm the efficacy of these drugs when administered for a shorter period and at much lower doses than the other drugs tested. The only nonnitroimidazole drugs that completely eliminated infection were albendazole, aminosidine, diethyl carbamazine and nitroscanate. Out of albendazole, aminosidine, diethylcarbamazine and nitroscanate antiparasitic drugs, the only one previously recommended for the treatment of infection by H. salmonis is aminosidine (15 g/kg feed for 3 consecutive days)13. Nitroscanate appears to have a rather broad activity spectrum, since it has been shown to be effective for bath treatment of Gyrodactylus14. Neither albendazole nor diethylcarbamazine has previously been shown to be effective for treatment of protozoan parasitoses of fishes. None of the antiparasitic drugs, viz., albendazole, aminosidine, diethylcarbamazine and nitroscanate showed the negative effects (signs of toxicity, behavioural effects, including anomalous swimming movements, rejection of food), suggesting that all four nitroimidazoles are viable options for the treatment of infection of salmonids by H. salmonis. This is of particular interest in view of the fact that H. salmonis strains apparently resistant to metronidazole have recently appeared on some farms6. Three drugs have been also been recommended for the treatment of protozoan parasitoses of fish, viz., amprolium8-9,13, bithionol6 and toltrazuril8-9,15. Of these, toltrazuril has been most widely used for the treatment of parasitoses of fish, and indeed this drug has been recommended for the treatment of various microsporidian and myxosporidian infections 15. This drug is not, however, effective for the treatment of infestation by the ectoparasitic ciliate Ichthyophthirius multifilils16. Among the amprolium, bithionol and toltrazuril, amprolium was found to be effective after oral administration; indeed, its administration by this route is recommended for myxosporidiosis. Bithionol and toltrazuril have been shown to be effective only in bath treatments. In a study of efficacy for the treatment of infestation by the flagellate Ichthyobodo necator, complete elimination of infestation in all fish assayed was achieved after bathing with bithionol at 25g 1-1 for 3 hr on 2 consecutive days, but not after bathing with amprolium or toltrazuril17. Nitroimidazoles are currently the only drugs recommended for oral treatment of H. salmonis infection. Earlier reports have recommended dimetndazole at the dose of 1.5 g/kg feed for 3 days13, Universal Journal of Pharmacy, 02(02), Mar-Apr 2013 xx Pandey et al. UJP 2013, 02 (02): Page 1-3 or at 15 g/kg feed for 4 to 7 days 8. Metronidazole has been recommended at doses of 0.5 mg/kg feed for 2 days7, 20 mg per/kg feed for 2 days4, or 1.5 g per/kg feed for 3 days. Bath treatment with metronidazole has been recommended for infections with Trichodina, Ambiphyra and Chilodonella6. www.ujponline.com 7. 8. CONCLUSION Severe morbidity and mortality have been noticed by the parasitic infection in fish. The ‘hexamitosis’ (caused by H. salmonis parasite) is probably the most frequent internal flagellate parasitosis of fish, particularly in the young salmonids. The H. salmonis infected fish pass both trophozoites and cysts in faeces. The oral treatment of this parasite can be done with the nitroimidazole group, which shows the activity against different protozoan groups, including flagellates and ciliates. Presently, the treatment of parasitic infection in fish can be done by dimetridazole or metronidazole given with feed. The nitroimidazoles, e.g., albendazole, aminosidine, diethylcarbamazine and nitroscanate can completely eliminate the parasite infection in the fish. Three drugs, viz., amprolium, bithionol and toltrazuril have been also been recommended for the treatment of protozoan parasitoses of fish. REFERENCES 9. 10. 11. 12. 13. 14. 1. Vickerman K. Phylum Zoomastigina. Class Diplomonadida. In: Margulis L, Corliss JO, Melkanian M, Chapman D, editors. Handbook of Protoctista. Boston: Jones and Barlett; 1989; p. 200-10. 2. Gratzek JB. Parasites associated with ornamental fish. Vet. Clin. North Am. Small Anim. Pract., 1988; 18: 375-99. 3. Woo PTK, Poynton SL. Diplomonadida, Kinetoplastida and Amoebida (Phylum Sarcomastigophora). In: Woo PTK, editor. Fish diseases and disorders, Vol. 1. Protozoan and metazoan infections. Wallingford: CAB International; 1995. p. 27-96. 4. Woo PTK. Flagellate parasites of fish. In: Kreier JP, editor. Pdrasitic Protozoa, Vol. 8. 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