Immunological effect of sparfloxacin in goats
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Abstract
In the present study, the immunological effects of a fluoroquinolone, sparfloxacin, were studied in goats after
multiple i.m. administration. Three groups of goats (4 goats in each) were selected. Group I consisted of saline control, Group II contained animals with antigen (Ag) control [2 ml of 7% sheep red blood cell (SRBC), Ag given on 1st day as sensitizing dose and on 10th day as challenging dose] and Group III consisted of animals exposed to sparfloxacin and SRBC Ag (Sparfloxacin @ 5 mg/kg i.m. daily for 7 days during sensitizing and challenging period and SRBC as given in Group II). The blood samples were collected on 1, 7, 10, 14, 21, 28, 35 and 42 days of the experiment. The immunological parameters evaluated were haemagglutination (HA) test for humoural immune response (HIR) whereas delayed type hypersensitivity (DTH) for evaluating cell mediated immune response (CMIR). DTH was assessed by injecting 1-chloro-2,4-dinitrobenzene (DNCB) and purified protein derivative (PPD) in the skin of the neck region as well as by absolute lymphocyte count. There was no significant effect of sparfloxacin on humoural immune response as assessed by HA test. DTH assessed by DNCB mitogen was significantly higher in sparfloxacin treated group as compared to antigen treated whereas in case of PPD mitogen there was no significant effect of the drug. Absolute lymphocyte count differed significantly in sparfloxacin treated group (6499.75±19.87) with antigen treated group (5485.00±19.87). Thus, it can be concluded that sparfloxacin has some immunomodulatory effect with respect to cell mediated immune response in goats.In the present study, the immunological effects of a fluoroquinolone, sparfloxacin, were studied in goats after multiple i.m. administration. Three groups of goats (4 goats in each) were selected. Group I consisted of saline control, Group II contained animals with antigen (Ag) control [2 ml of 7% sheep red blood cell (SRBC), Ag given on 1st day as sensitizing dose and on 10th day as challenging dose] and Group III consisted of animals exposed to sparfloxacin and SRBC Ag (Sparfloxacin @ 5 mg/kg i.m. daily for 7 days during sensitizing and challenging period and SRBC as given in Group II). The blood samples were collected on 1, 7, 10, 14, 21, 28, 35 and 42 days of the experiment. The immunological parameters evaluated were haemagglutination (HA) test for humoural immune response (HIR) whereas delayed type hypersensitivity (DTH) for evaluating cell mediated immune response (CMIR). DTH was assessed by injecting 1-chloro-2,4-dinitrobenzene (DNCB) and purified protein derivative (PPD) in the skin of the neck region as well as by absolute lymphocyte count. There was no significant effect of sparfloxacin on humoural immune response as assessed by HA test. DTH assessed by DNCB mitogen was significantly higher in sparfloxacin treated group as compared to antigen treated whereas in case of PPD mitogen there was no significant effect of the drug. Absolute lymphocyte count differed significantly in sparfloxacin treated group (6499.75±19.87) with antigen treated group (5485.00±19.87). Thus, it can be concluded that sparfloxacin has some immunomodulatory effect with respect to cell mediated immune response in goats.
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References
Ansari M K, Sinha S P, Jayachandran C and Singh M K. 2000. Pharmacokinetics and distribution of pefloxacin in biological fluids of locatating goats after intravenous administration. Indian Journal of Animal Research 34: 95–99.
Arfa Majeed, Aqeel Javeed, Muhammad Ovais Omer, Muhammad Hassan Mushtaq and Adeel Sattar. 2020. Evaluation of immunomodulatory effects of lomefloxacin in mice. Brazilian Journal of Pharmaceutical Science 56: 18669. DOI: https://doi.org/10.1590/s2175-97902019000418669
Baggot J D. 2001 Antimicrobial disposition, selection, administration and dosage, Pp. 210-251. The Physiological Basis of Veterinary Clinical Pharmacology. Blackwell Science Ltd., Osney Mead, Oxford, London, U.K.
Badari M S, Elgendy S G, Mohamed A S and Hassan A T. 2015. Immunomodulatory effects of levofloxacin on patients with pneumonia in Assiut University Hospitals. Egypt Journal of Immunology 22(1): 85–91.
Chauhan H V S and Verma K C. 1983. Evolution of cell mediated immunity to Marek” disease. Brazilian Veterinary Journal 139: 57–65. DOI: https://doi.org/10.1016/S0007-1935(17)30582-1
Dalhoff A and Shalit I. 2003. Immunomodulatory effects of quinolones. Lancet Infectious Diseases 3(6): 359–71. DOI: https://doi.org/10.1016/S1473-3099(03)00658-3
Dalhoff A. 2005. Immunomodulatory activities of fluoroquinolones. Lancet Infectious Disease 33: 55–70. DOI: https://doi.org/10.1007/s15010-005-8209-8
Dhiraj. 2007. ‘Pharmacokinetic and immunological interaction of enrofloxaicn with ketoprotein.’ MVSc Thesis. Submitted to RAU, Pusa, Samastipur, India.
Jose Honeegowda, Jayakumar K, Krishnappa G and Narayana K. 1999. Effect of simultaneous administration of pefloxacin and diclofenac sodium on natural host defence mechanism and immune response in rabbit. Indian Journal of Pharmacology 31: 358–62.
Kabat E A and Mayer M M. 1961. Experimental Immunochemistry. (Ed.) Chales C. Thomas Publishers, Spring Field, Ilinoss, USA.
Kaku M, Ishida K, Mizukane R, Take Myra, Yoshida R, Tanaka H, Usui T, Tomono K and Suyama N. 1994. In vitro and in vivo activities of sparfloxacin against mycoplasma pneumonia. Antimicrobial Agent Chemotherapy 38(4): 738-41. DOI: https://doi.org/10.1128/AAC.38.4.738
Kujur R S. 2005. ‘Pharmacokinetic study of sparfloxacin in healthy febrile goats.’ MVSc Thesis. BAU, Ranchi, India.
Manzella J P and Clark J K. 1988. Effects of quinolones on mitogen stimulated human mononuclear leukocytes. Journal of Antimicrobial Therapeutics 21: 183–86. DOI: https://doi.org/10.1093/jac/21.2.183
Kumar N, Singh S D and Jayachandran C. 2003. Pharmacokinetic study of diclofenac and its interaction with enrofloxacin in buffalo calves. Journal of Veterinary Science 4: 155–59. DOI: https://doi.org/10.4142/jvs.2003.4.2.155
Kumar N. 2005. ‘Pharmacokinetics and immunological interaction of pefloxacin, with ketoprofen.’ Ph.D. Thesis. R.A.U. Pusa, Samastipur, Bihar.
Shalit I. 1991. Immunological aspects of new quinolones. European Journal of Clinical Microbiology and Infectious Diseases 10: 262–66. DOI: https://doi.org/10.1007/BF01966999
Shimada J, Nogita T and Ishibasti Y. 1993. Clinical pharmacokinetics of sparfloxain. Journal of Clinical Pharmacokinetics 25(5): 358–69. DOI: https://doi.org/10.2165/00003088-199325050-00002
Thompson C D, Whittingham S, Mackay I R, Khoo S K, Toh B H and Siage R J. 1975. Quantitation of cell mediated immune response to dinitrochlorobenzene and ubiquitous antigens. Compendium of Canadian Medical Association 102: 1074– 78.
Trautmann M, Ruhnke M, Borner K, Wagner J and Koeppe P. 1996. Pharmacokinetics of sparfloxacin and serum bacteriual of activity against penuymococci. Antimicrobial Agent Chemotherapy 40(3): 776–79. DOI: https://doi.org/10.1128/AAC.40.3.776
Tripathi K D. 2003. Essential Medical Pharmacology. 5th Edn. Jaypee, Medical Publishers, p651.
Zix J A, Geerdes – Fenge H F, Rau M, Vockler J, Borner K, Koeppe P and Lode H. 1997. Pharmacokinetics and sparfloxacin and interaction with cisapride and sucralfate. Antimicrobial Agent Chemotherapy 41(8): 1668–72. DOI: https://doi.org/10.1128/AAC.41.8.1668
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