K.M. Alsaad* and O.M. Al-Iraqi

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Original Article Buffalo Bulletin (September 2010) Vol.29 No.3 COMPARISON OF THERAPUTICAL EFFICACY OF ALBENDAZOL, LEVOZAN AND IVERMECTINE IN TREATMENT OF BUFFALOES NATURALLY INFECTED WITH GASTRO-INTESTINAL WORMS IN MOSUL, IRAQ K.M. Alsaad* and O.M. Al-Iraqi ABSTRACT The object of this study is to compare the efficacy of a single dose of albendazol (Group 1) (10 mg/kg. BW oral suspension) and a single dose 2.5 ml/10 kg. BW. of levozan (Group 2) oral suspension (a mixture of levamisole and oxyclozanide) and ivermectine (Group 3) 0.2 mg/kg. BW. (S.C injection) for one time in the treatment of buffaloes naturally infected with Thirty buffaloes of local breed 6 months to more than 4 years old were used in this study, the animals were divided into three equal groups (10 buffaloes for each). Based on the number of days taken for parasitological cure, and mean reduction EPG. Total erythrocytes count (RBCs), hemoglobin concentration (HB), packed cell volume (PCV), total platelets count (Plt) and erythrocytes sedimentation rate (ESR), were also encountered pre-and post treatment. Results indicated reduction in EPG to zero on the 7 th day post treatment (Group 1) which also showed a significant increase in RBCs, HB, PCV and Plt and a significant decrease in ESR on the 14 th day post treatment,while there was gradual reduction of EPG without complete elimination of total eggs count on day 21 of treatment with Groups (2) and (3). Levosan was found highly effective in the treatment of buffaloes naturally infested with Keywords: efficacy, albendazole, levosan, ivernectine, buffaloes, gastrointestinal worms INTRODUCTION Buffaloes are considered as one of the most important sources of milk and meat production (AL- Jamass, 1999) However, they can become infested with different types of parasitic gastro-intestinal worms resulting in serious effects and health deterioration, leading to substantial economic losses (Solusby, 1986, El-Sherif et al., 1999). Gastro-intestinal worms which comprise nematodes such as Osretagia, Trichostrongylus, Hemonchus, Cooperia, Toxocara, Marshelagia and Cestodes such as Monezia spp., and others, affect the health of animals and their productivities and also decrease resistance to diseases which adversely effect the nutritional status and even cause severe mortalities (Jithendran and Bhat, 1999). The anthelmintic activities and therapy of albendazol, levozan and ivermectin have been studied (Kasarilikar et al., 1997, Dale and Haylett, 2004). Albendazol act by inhibiting tubulin polymerization (Adams, 2001), ivermectine produces flaccid paralysis of parasites by acting as an agonist of the neurotransmitter gammaaminobutyric acid (GABA), thereby disrupting GABA-mediated central nervous system (CNS) Department of Internal and Preventive Medicine, College of Veterinary Medicine, University of Mosul, Mosul, Iraq *E-mail: allsaad2008@yahoo.com 189

neurosynaptic transmission (Einstein et al., 1994; Dacasto and Cocuzza, 1995), whereas oxyclozanide is a salicylanilde anthhelmentic that acts by uncoupling oxidative phosphorylation, thereby decreasing the availability of high energy phosphates such as ATP to the parasites; it is formulated as an oral drench containing oxyclozanide alone or in combination with levamisole hydrochloride (Einstein et al., 1994). The goal of this study was to compare the therapeutic efficacy of albendazole, levozan and ivermectin in buffaloes naturally infested with the 7 th, 14 th and 21 th days of treatment. Blood collection and hematology Five milliliters of blood drained from each animal by jugular vein-puncture and mixed with EDTA were used to determine RBCs, HB, PCV, Plt (Automatic Full Digital Cell Counter, Beckman, USA), and ESR by westergren method (Meyer and Harvey, 2004). Statistical Analysis The data were analyzed statistically using SPSS version 11.5 (SPSS Inc., 2002) MATERIALS AND METHODS RESULTS Animals and study design The study was conducted on thirty local breed buffaloes 6 months and more than 4 years old, naturally infested with gastro-intestinal worms, such as Osretagia spp., Trichostrongylus spp Hemonchus spp., Cooperia spp., and the worm of Monezia expansa, Toxocara vitulorum, Marshelagia marshalli. Animals were divided randomly into three equal groups (10 animals in each). Single doses of Albendazol 10 mg/kg BW oral suspension (Group 1) (Alfabendazole, Alleppo Laboratories for Veterinary products, Syria), levozan (Group 2) (a mixture of oxyclozanide and levamisole) at the manufacturer s recommended dose rate of 2.5 ml/ 10 kg BW oral suspension (Levozan, Veterinary and Agricultural Products, VAPCO-Jordan) and Ivermectine (Group 3) 0.2 mg/kg. BW (S/C) injection one time (Evanomic, Prima Ingredients S.L, Spain), were evaluated for therapeutic efficacy and to assess the efficacy of the drugs, fecal samples of all infested buffaloes were examined with respect to reduction of eggs on Levosan (Group 1) which was given to infected buffaloes as oral suspension at the dose rate of 2.5 ml/kg. BW, showed the cent percent efficacy on 7 th day of treatment and continued to the day 21 th, whereas gradual reduction of egg counts where encountered in Group (2 and 3), Table 1. With respect to hemogram (Table 2), there were significant increases in the mean values of RBCs, HB, and PCV, with a significant decrease in ESR in Group (1) on the 14 th day of treatment trial, but no differences in these values were indicated in Groups (2 and 3). DISCUSSION Results of the present study showed high efficacy of levosan (amixture of levamesol and oxyclozanide) for complete and fast removal of worms eggs. The drug was well tolerated and with no evidence of drug associated toxicity was noticed in any of treated animals, similar 190

Table 1. Eggs per gram (EPG) of buffaloes naturally infected with gastro-instetinal worms pre and post treatment. Parameter Groups Pretreatment Post-treatment 7 days 14 days 21 days Group I 1211 a ±215 0 b 0 B 0 b EPG Group II 1120 a ±119 800 b ±170 206 C ±70 98 d ±11 Group III 1050 a ±168 753 b ±200 117 C ±88 55 d ±18 Values are (mean±standard error of mean). Values with different letters mean: the presence of significant differences (P<0.05). Table 2. Hematological parameters of buffaloes naturally infected with gastro-intestinal worms pre and post treatment. parameters Groups Pretreatment Post-treatment 7 days 14 days 21 days Group I 5.02 a ±1.633 5.9 a ±1.89 7.3 b ±0.29 7.6 b ±0.8 RBCs Group II 5.22 a ±0.96 5.8 a ±0.33 6.1 a ±0.72 6.1 a ±0.95 Group III 5.6 a ±0.33 5.1 a ±1.81 6.3 a ±0.28 6 a ±0.92 Group I 9.6 a ±1.65 10 a ±0.85 12.1 b ±1.21 12 b ±1.6 HB Group II 9.8 a ±0.99 10.2 a ±0.82 9.9 a ±1.22 10.1 a ±0.6 Group III 10 a ±0.78 9.8 a ±0.69 9.7 a ±0.55 10 a ±0.91 Group I 26.8 a ±2.11 28 a ±3.11 34 b ±1.29 33 b ±2.21 PCV Group II 27 a ±1.99 27 a ±2.39 29 a ±3.1 24 a ±2.6 Group III 28 a ±0.82 27 a ±1.66 28 a ±2.2 28 a ±3.39 Group I 225 a ±30.11 259 a ±37.5 233 b ±5.1 321 b ±33.2 Plt Group II 230 a ±40.2 250 a ±55.6 237 a ± 40.4 144 a ±21.4 Group III 251 a ±31.4 266 a ±39.5 244 a ±20.3 149 a ±33.2 Values are (mean ± standard error of mean). Values with different letters mean: the presence of significant differences (P<0.05). 191

results were also recorded by (Kasarilikar et al., 1997) as the oxyclozanide act by uncoupling oxidative phosphorylation, thereby decreasing the availability of high energy phosphates such as ATP to the parasites. Moreover, levamisole acts by making tonic paralysis of the parasites, which gives the mixture a wide range of anti parasitic activity (Riviere and Papich, 2009). Ivermectin acts on the GABA system of the nervous tissues and has little or no activity on some worms like cestods (Vermunt and Pomroy, 1995), beside some resistance which was recorded for albendazole (Figueroa et al., 2000; Hoque et al., 2003; Sissay et al., 2006). The anthelmintic resistance to albendazole is usually notice when worm control policies fail dramatically; however, resistance is present when there is a greater frequency of parasites in population able to tolerate doses of a compound than in the normal population of the same species. The problem of anthelmintic albendazole has been reported (Mckenna, 1996; Familton et al., 2001), it is thought that regular suppressive dosing had probably resulted in anthelmintic resistance in many countries. Schwab et al. (2005) added that many helminth parasites have developed resistance against both albendazole and ivermectin and they thought that the resistance to albendazole is known to be caused by either of two single amino acid substitutions from phenylalanine to tyrosine in parasite beta-tubulin at position 167 or 200. CONCLUSIONS Levosan has a wide range of anti parasitic activity compared to albendazole and ivermectin in the treatment of buffaloes naturally infested with ACKNOWLEDGEMENT This article was supported by the College of Veterinary Medicine, University of Mosul, Iraq. REFERENCES AL-Jamass, R.K. 1999. Determination of some featural and production traits on Iraqi water buffalo in Badosh. Buffalo Newsletter, 12: 12-13. In FAO/RNE. Regional office for the Near East, Cairo, 2004. Dacasto, M. and U.I. Cocuzza. 1995. Efficacy of ivermectin in reducing gastrointestinal nematode fecal egg counts in goats in Burundi. Prev. Vet. Med., 23(3-4): 73-178. Dale, M.M. and D.G. Haylett. 2004. Pharmacol., 1 st ed. Chirchill Livingston. Elseveier Ltd. UK. p. 109-110. Einsteinm, R., R.S. Jones, A. Knifton and G.A. Starmer. 1994. Principles of Veterinary Therapeutics, Logman Scientific and Technicals. p. 490-507. El-sherif, A.M., M.A. Abdel-gawad, H.S. Lotfy, K.A. Shokier. 2000. Impact of gastrointestinal nematodes and some enteric protozoal affection on the health of buffaloe calves. Assiut Vet. Med. J., 43: 260-270. Familton, A.S., P. Mason and G.C. Coles, 2001. Anthelmintic resistance of Cooperia species in cattle. Vet. Rec., 149(23): 719-720. Figueroa, C.J.A., M.R.D. Mendez, V.J.M. Berruecos and L.J.A. Alverez. 2000. Resistance of Hemonchus contortus to injectable albendazole sulfoxide using the egg reduction count technique in sheep. Vet. Mex., 31(4): 309-313. Hoque, M.N., N. Begum and M. Nooruddin. 2003. 192

Albendazole Resistance in gastro-intestinal Nem parasites of cattle in Bangladesh. Trop. Anim. Health Prod., 35: 219-222. Jithendran, K.P. and T.K. Bhat. 1999. Epidemiology of parasitoses in dairy animals in the north west humid Himalaya region in India with references to gastro-intestinal nema-todes. Trop. Anim. Health Prod., 31: 205-214. Kasarilikar, V.R., S.P. Kumar, K.G. Udupa, B.V. Shivaparkash, N.A. Patial and A.B. Mutnal. 1997. Comparative efficacy of levamisole against ascariasis in buffaloe calves. Ind. Vet. J., 76: 150-152. Mckenna, P.B. 1996. Anthelmintic resistance in cattle nematodes in New Zeland: Is It increasing. New Zeland Vet. J., 44(76): 76-77. Meyer, D.J. and J.W. Harvey. 2004. Veterinary Laboratory Medicine: Interpretation and Diagnosis, 3 rd ed. Saunders, Elsevier Inc, USA. pp: 156-160. Riviere, J.E. and M.G. Papich. 2009. Veterinary Pharmacology and Theraputics, 9 th ed. John Wiley and Sons. p. 1107-1110. Sissay, M.M., A. Asefa, A. Uggla and P.J. Waller. 2006. Anthelmintic of nematode parasites of small ruminants in eastern Ethiopia: exploitation of refugia to restore anthelmintic efficacy. Vet. Parasitol., 18; 135(3-4): 337-346. Solusby, E.J.L. 1986. Heilminths, Arthropods and Protozoa of Domesticated Animals, 7 th ed. Philadelphia, Bailliere Tindall, London. p. 3-4. Statistical Package for the Social Science Advance Statistics TM Version 11.5. 2002. SPSS Inc., Chicago, IL. Vermunt, J.J. and W.W. Pomroy. 1995. Multiple resistance to ivermectine and oxefendazole in Cooperia species of cattle in New Zealand. Vet. Rec., 13(2): 43-45. 193