Summary
Administration of antibiotics is considered an important factor during, or after, operational procedures in the maxillofacial area, in order to avoid post-surgical complications. In the present study, the levels of quinolones in serum and tissues such as the parotid gland, the tongue and the bone of the jaws were estimated during traumatic injury in the oral cavity. For this purpose, two groups (A and B) of Wistar rats, consisting of 35 animals each were used. Group A (control) and group B (experimental) were divided in five subgroups (A1, A2, A3, A4, A5 and B1, B2, B3, B4, B5). In the experimental group, model traumatic injury was performed through the whole length of the cheek. Subjects received orally ciprofloxacin, pefloxacin, norfloxacin, ofloxacin and cinoxacin. The concentration of quinolones in serum and in most of the tissues was significantly higher, in the experimental groups than in controls. In addition, the FFA levels and the weight of adrenals (as indicators of stress) were higher in the trauma groups. Stress seemed to affect many pathophysiological mechanisms which are responsible for the alterations observed.
Similar content being viewed by others
References
Driewer C.W., Bousquet W.F. (1965): Stress-induced interactions: evidence for rapid enzyme induction. Life Sci., 4, 1449–1454.
Furner R.L., Stitzel R.E. (1968): Stress-induced alterations in microsomal drug metabolism in the adrenalectomised animal. Biochem. Pharmacol., 10, 121–127.
Sfikakis A., Galanopoulou P., Konstandi M., Tsakayannis D. (1996). Stress through handling for vaginal screening, serotonin and ACTH response to ether. Pharm. Biochem. Behav., 53, 965–970.
Birke, G., Carlsson L.A., Liljedahl S-O. (1965): Lipid metabolism and trauma. III. Plasma lipids and lipoproteins in burns. Acta Med. Scand., 178, 337–350.
Elfstrom J., Johansson H., Lindgren S. (1978): The human metabolism of phenazone after hydrocortisone administration. Eur. J. Clin. Pharmacol., 13, 69–70.
Tsopanakis C., Tesserommatis C. (1991): Cold swimming stress: effects on serum lipids, proteins, lipoproteins and LCAT activity in male and female rats. Pharm. Biochem. Behav., 38, 813–816.
Tesserommatis C., Tsopanakis C., Symeonoglou G., Loukissa M., Varonos D. (1996). How harmless is FFA enhancement? Eur. J. Drug Metab. Pharmacokinet., 21, 213–215.
Kinney J.M., Long C.L., Duke J.H. (1970): Carbohydrate and nitrogen metabolism after injury. In: Porter and Knight (eds). Energy Metabolism in Trauma. London: Churchill Livingstone, 103–126.
Thoren L. (1975): Metabolic response to injury. Surg. Annu., 7, 53–70.
Johnston I.D.A., Welbourn R.B. (1970): Metabolic and endocrine response to trauma. Surg. Annu. 8, 91–101.
Lucas C.E. (1976): The renal response to acute injury and sepsis. Surg. Clin. North Am. 56, 953–975.
Patton J.H., Reeves D.S. (1988): Fluoroquinolone antibiotics. Microbiology, pharmacokinetics and clinical use. Drugs, 36, 193–228.
Bergan T. (1988): Pharmacokinetics of fluorinated quinolones. In: Andriole V.T. (ed) The Quinolones. Bayer: Academic Press, 119–154.
Bergan T. (1987): Pharmacokinetic properties of the cephalosporins. Drugs, 34 Suppl. 2, 89–104.
Bennet VJ., Brodie L.J., Benner L.E., Kirby N.W. (1966): Simplified accurate method to antibiotic of clinical specimens. Appl. Microbiol., 14, 170–177.
Omrani R.G., Furnkawa H., Sherwood I., Loeb J. (1983): [3H]-Dexamethazone binding by rat liver microsomes Effects of age, sex and adrenal status. Endocrinology, 112, 178–186.
Kant G.J., Bunnell B.N., Mougey E.H., Pennington L.L., Meyerhoff J.L. (1983). Effects of repeated stress on pituitary cyclic AMP, and plasma prolactin, corticosterone and growth hormone in male rats. Pharmacol. Biochem. Behav., 18, 967–971.
Pollack G.M., Browne J.L., Marton J., Haberer L.J. (1991): Chronic stress impairs oxidative and hepatic excretion of model xenobiotic substrates in the rat. Drug Metab. Dispos., 19, 130–134.
Borga O., Piafsky K.M., Nilsen O.G. (1977): Plasma protein binding of basic drugs: I. Selective displacement from α1-acid glycoprotein by Tris (2-butoxyethyl) phosphate. Clin. Pharmacol. Ther., 22, 539–544
Fremstad D., Bergerud K., Haffner J.F.W.et al. (1976): Increased protein binding of quinidine after surgery: a preliminary report. Eur. J. Clin. Pharmacol., 10, 441–446.
Soltys B.J., Hsia J.C. (1978): Steroid modulation of human serum albumin binding properties. A spin label study. J. Biol. Chem., 253, 4266–4269.
Oie S., Torer T.N. (1979): Effect of altered plasma protein binding on apparent volume of distribution. J. Pharm. Sci., 68, 1203–1208.
Caffruny E.L. (1977): Renal tubular handling of drugs. Am. J. Med., 62, 491–502.
Goodman and Gilman’s (1996): The Pharmacological Basis of Therapeutics, 9th edn. New York: McGraw-Hill Health Division, p. 746.
Speight T.M., Holford N.H.G. eds. (1997): Avery’s Drug Treatment, 4th edn. Auckland: Adis International, pp. 34–35
Upton R.A., Williams R.L., Buskin J.N., Jones R.M. (1982): Effects of probenecid on ketoprofen kinetics. Clin. Pharmacol. Ther., 31, 705–712.
Konig E., Lemp A. (1966): Plasmavolumenanderungen durch alltaglich Belastungen bei Herzgesunden und Herzinsuffizienten. Klin. Wochenschr., 44, 862–870.
Ylitalo P., Hinkka H., Neuvonen P. (1977): Effect of exercise on the serum level and urinary excretion of tetracycline and sulphamethizole. Eur. J. Clin. Pharmacol., 12, 367–373.
Stizel R.E., Furner R.L. (1967): Stress induced alterations in microsomal drug metabolism in the rat. Biochem. Pharmacol. 16, 1489–1494.
Rauckman E.J. Rosen G.M., Post S.E., Gillogly S.D. (1980): Effect of model traumatic injury on hepatic drugmetabolizing enzymes. J. Trauma, 20, 884–886.
Griffeth L.K., Rosen G.M., Tschanz C., Rauckman E.J. (1983): Effects of model traumatic injury on hepatic drug metabolism in the rat. I.In vivo antipyrine metabolism. Drug Metab. Dispos., 11, 517–525.
Griffeth L.K., Rosen G.M., Rauckman E.J. (1983): Effects of model traumatic injury on hepatic drug metabolism in the rat. V. Sulfation and acetylation. Drug Metab. Dispos., 13(4), 398–405.
Griffeth L.K., Rosen G.M., Rauckman E.J. (1987): Effects of model traumatic injury on hepatic drug metabolism in the rat. VI. Major detoxification/toxification pathways. Drug Metab. Dispos., 15, 749–759.
Mahr U., Sorgel F., Naber K., Schumacher H., Gruber G. (1987): Penetration of norfloxacin (NOX) into body fluids of healthy volunteers. Abstr. Proc. 15th ICC, Istanbul, Turkey.
Malter U., Jaehde U., Sorgel F., Stephan U., Hoffler D. (1987): Individual factors affecting the pharmacokinetics of pefloxacin (PEF). Abstr. Proc. 15th ICC, Istanbul, Turkey.
White L., Macgowan A.P., Lovering A.M., Reeves D.S., Mackay A.P. (1987): The kinetics of ofloxacin desmethyl-ofloxacin and ofloxacin N-oxide in patients with chronic renal failure. Abstr. Proc. 15th ICC, Istanbul, Turkey.
Christ W. (1987): Betrachtungen zum metabolitenmuster der quinolone mit Piperazinsubstituenten. Fortschritte der antimikrobiellen u. antineoplastischen Chemotherapie, 6–10, 2157–2161.
Kalager T., Digranes A., Bergan T., Rolstad T. (1985): Pharmacokinetics of Ofloxacin in serum and skin blister. Proc. of the 14th ICC, Kuoto, 1985. In: Recent Advances in Chemotherapy. Antimicrobial Section 2. Tokyo: University of Tokyo Press, pp. 1765–1766.
Wise R., Lockley R., Webberly M.J., Dent J. (1984): The pharmacokinetics and tissue penetration of enoxacin and norfloxacin. J. Antimicrob. Chemother., 14 Suppl. C, 75–81.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Trichilis, A., Tesserommatis, C. & Varonos, D. Changes in serum levels of quinolones in rats under the influence of experimental trauma. Eur. J. Drug Metab. Pharmacokinet. 25, 73–78 (2000). https://doi.org/10.1007/BF03190070
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF03190070