30-Title: Safety assessment of amikacin after repetitive intramuscular administration in goats

30-Title: Safety assessment of amikacin after repetitive intramuscular administration in goats

Authors: Namrata Upadhyay, Nitesh Kumar, Arpita Shrivastav, Swatantra Singh, Neeraj Shrivastava, Jitendra Kumar and Rajeev Ranjan

Source: Ruminant Science (2021)-10(1):155-159.

How to cite this manuscript: Upadhyay Namrata, Kumar Nitesh, Shrivastav Arpita, Singh Swatantra, Shrivastava Neeraj, Kumar Jitendra and Ranjan Rajeev (2021). Safety assessment of amikacin after repetitive intramuscular administration in goats. Ruminant Science 10(1):155-159.

Abstract

Amikacin is an aminoglycoside antibiotic used to treat infections caused by more resistant strains of Gram-negative bacteria and some Gram-positive bacteria. Clinically low therapeutic index of this antibiotic may lead to adverse changes in haemato-biochemical and urine parameters, especially associated with liver and kidney. Amikacin (10 mg/kg b.wt.) was administered through an intramuscular route repeatedly for 5 days in four healthy non-lactating female goats. Blood samples were collected on days 0, 2nd, 4th and 6th and analyzed by using standard diagnostic kits. There was a significant (p<0.05) increase in plasma creatinine and blood urea nitrogen levels on day 4th, with no significant change in blood haemoglobin, packed cell volume, total erythrocytes count, total leucocytes counts, lymphocytes, monocytes, eosinophils, basophils and neutrophils and the serum albumin, globulin, total protein, bilirubin, cholesterol and triglyceride concentration on the 0, 2nd, 4th and 6th day were observed. Further significant (p<0.05) increase in alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase levels were observed during the course of amikacin administration. Urine analysis did not show any significant change in specific gravity, pH, pus cells and epithelial cells, and other parameters like bile salt, ketone body, albumin, RBCs, cast and crystal were not detected in urine during the entire study period. The results conclude that amikacin did not alter the haemato-biochemical and urine parameters, in female goats after repeatedly intramuscular administration at therapeutic dose.

References

Anitha R, Vijayaraghavan R, Geetha RV, Anitha M, Priya SV, Anusha R, Vidyalakshimi U, Namrata KR, Mohan SK and Chakkaravarthy M (2016). A comparative study of the effect of amikacin administered through autoinjector and manual injection on biochemical parameters in rats. Journal of Applied Pharmaceutical Science 6(2):109-114.

Bain VG (2003). Hepatorenal syndrome, hepatopulmonary syndrome, and now, hepatospinal syndrome? Liver Transplantation 9(9):995-996.

Begg EJ and Barclay ML (1995). Aminoglycosides 50 years on. British Journal of Clinical Pharmacology 39:597-603.

Dinev T, Kanakov D and Zapryanova D (2005). Investigations on some biochemical and Haematological parameters after tobramycin and amikacin treatment in female goats. Trakia Journal of Sciences 3(5):14-16.

Ezhilarasan D, Karthikeyan S and Vivekanandan P (2012). Ameliorative effect of silibinin against N-nitroso-dimethylamine induced hepatic fibrosis in rats. Environmental Toxicology and Pharmacology 34:1004-1013.

Fischbach FA (2000).  Manual of Laboratory and Diagnostic Tests. 6th Edn, Lippincott, Philadelphia.

Glasby S (1976). Encylopedia of Antibiotics. Wiley, London.

Gregory CR (2003). Urinary system. In: Veterinary Laboratory Medicine and Clinical Pathology. 4th Edn. Eds: KS Latimer, EA Mahaffe and KW Prasse, Duncan and Prasse’s. Ames, Iowa State Press.

Hsu LY, Kwa AL, Lye DC, Chlebicki MP, Tan TY, Ling ML, Wong, SY and Goh LG (2008). Reducing antimicrobial resistance through appropriate antibiotic usage in Singapore. Singapore Medical Journal 49(10):749-755.

Jain NC (1986). Schalm’s Veterinary Haematology. 4th Edn. Lea and Febiger, Philadelphia.

Jernigan AD, Hatch RC and Wilson RC (1988). Pharmacokinetics of tobramycin in cats. American Journal of Veterinary Research 49:608-612.

Kaneko JJ, Harvey JW and Bruss ML (1997). Clinical Biochemistry of Domestic Animals. 5th Edn. Academic Press, San Diego, California, USA.

Kaynar K, Gul S, Ersoz S, Ozdemir F, Ulusoy H and Ulusoy S (2007). Amikacin-induced nephropathy: Is there any protective way? Renal Failure 29(1):23-27.

Langhendries JP, Battisti O, Bertrand JM, François A, Darimont J, Ibrahim S, Tulkens PM, Bernard A, Buchet JP and Scalais E (1993). Once a day administration of amikacin in neonates: Assessment of nephrotoxicity and ototoxicity. Developmental Pharmacology and Therapeutics (Basel) 20:220-230.

Lashev L and Lasarova S (2001). Pharmacokinetics and side effects of gentamicin in healthy and Pseudomonas aeruginosa infected sheep. Journal of Veterinary Pharmacology and Therapeutics 24:237-240.

Masakazu K, Yoshiko E and Masashi E (2014). Acquired resistance of Listeria monocytogenes in and escaped from liver parenchymal cells to gentamicin is caused by being coated with their plasma membrane. Microbes and Infection 16(3):237-243.

Mayer DJ and Harvey JW (2004). Veterinary Laboratory Medicine, Interpretation and Diagnosis. Saunders, Philadelphia.

Nayma S, Sadia CSM, Tanveer HP and Jesmine A (2012). Effects of Ashwagandha (Withania somnifera) root extract on some serum liver marker enzymes (AST, ALT) in gentamicin intoxicated rats. Journal of Bangladesh Society of Physiologist 7(1):1-7.

Parlakpýnar H, Ozer MK, Ucar M, Gaffaroglu M, Vardi N, Koc M and Acet A (2006). Protective effects of caffeic acid phenethyl ester (cape) on amikacin induced nephrotoxicity in rats. Cell Biochemistry and Function 24:363-367.

Peloquin CA, Berning SE, Nitta AT, Simone PM, Goble M, Huitt GA, Iseman MD, Cook JL and Curran-Everett D (2004). Aminoglycoside toxicity: daily versus thrice-weekly dosing for treatment of mycobacterial diseases. Clinical Infectious Diseases 38:1538-1544.

Plumb DC (2008). Veterinary Drug Handbook. 6th Edn. Stockholm, Ames, Iowa: Distributed by Blackwell Publication.

Ramsay EC and Vulliet R (1993). Pharmacokinetic properties of gentamicin and amikacin in the Cockatiel. Avian Diseases 37:628-634.

Shils ME (1963). Renal disease and the metabolic effects of tetracycline. Annals of Internal Medicine 58:389-408.

Vasquez-Mendoza G, Vargas-Origel A, Ramos-Jimenez AC, Aguilar-Orozco G and Romeo-Gutierrez G (2007). Efficacy and renal toxicity of one daily dose of amikacin versus conventional dosage regime. American Journal of Perinatology 24:141-146.