Pharmacokinetic behavior of marbofloxacin after intravenous and intramuscular administrations in adult goats.

The pharmacokinetic behavior of marbofloxacin was studied in goats after single-dose intravenous (i.v.) and intramuscular (i.m.) administrations of 2 mg/kg bodyweight. Drug concentration in plasma was determined by high performance liquid chromatography (HPLC) and the data collected were subjected to compartmental and noncompartmental kinetic analysis. This compound presented a relatively high volume of distribution (Vss=1.31 L/kg), which suggests good tissue penetration, and a total body clearance (Cl) of 0.23 L/kg small middle doth, which is related to a long elimination half-life (t1/2beta=7.18 h and 6.70 h i.v. and i.m., respectively). Pharmacokinetic parameters were not significantly different between both routes of administration. Marbofloxacin was rapidly absorbed after i.m. administration (Tmax=0.9 h) and had high bioavailability (F=100.74%).

Haemorrhagic septicaemia by Aeromonas salmonicida subsp. salmonicida in a black-tip reef shark (Carcharhinus melanopterus).

One black-tip reef shark (Carcharhinus melanopterus) was found dead without previous signs of disease. Major lesions consisted in cutaneous erythema, mainly at the base of the fins, focal to diffuse inflammatory lesions in gills and intestinal wall, and discrete haemorrhages in the same organs, liver and kidneys. Microcolonies of Gram-negative rods were observed in the lamina propia of gills, underneath the intestinal mucosa and randomly distributed in the renal and hepatic parenchymas. Also, emboli containing Gram-negative rods were observed in capillaries of these organs. Aeromonas salmonicida subsp. salmonicida was isolated in pure culture from gills, liver and intestine. Specific immunostaining confirmed the relationship between the isolate and lesion-associated bacteria. No previous reports on this infection in sharks have been found in the literature.

Effects of verapamil, sodium nitroprusside and calcium deprivation on the phenylephrine-induced contraction of smooth muscle strips from the reticular groove of adult cattle.

The effects of verapamil, sodium nitroprusside and calcium deprivation on the smooth muscle strips from the floor of the reticular groove of adult cattle were studied. The mechanical activity of the muscle strip was recorded isometrically. Contraction was induced with phenylephrine (10(-6) mol/l) in Tyrode solution. Verapamil (10(-6) mol/l) produced a high inhibition of the response, phasic and tonic (P < 0.05). Sodium nitroprusside (10(-6) mol/l) reduced mainly the phasic contraction (P < 0.05). Deprivation of Ca2+ from extracellular medium produced a high inhibition of the tonic phase. This study indicates that the action of verapamil on the reticular groove smooth muscle may be partially related to blockade of calcium entry through voltage-dependent channels, opened during phenylephrine stimulation. However, the nitroprusside action could be attributed to effect on the extrusion of calcium.

Age-related differences in norfloxacin pharmacokinetic behaviour following intravenous and oral administration in sheep.

The pharmacokinetics of norfloxacin after intravenous (i.v.) and oral (PO) administration in lambs (n = 5) and adult sheep (n = 5) were studied. After i.v. administration (10 mg.kg-1) plasma concentrations were best fitted by a three-compartment open model in both age groups. Distribution volumes were significantly larger in lambs (approximate 4.0 fold difference between 4 week old and adult sheep). There was no significant difference (p < 0.05) between the groups in terms of elimination halflife but plasma clearance was significantly higher in lambs. Norfloxacin was poorly absorbed after oral administration (60 mg.kg-1) in sheep (F = 4.04%). Mean oral bioavailability was 73.51% in lambs (30 mg.kg-1). Norfloxacin elimination was faster in lambs after oral administration. MRTt was significantly prolonged in both age groups when compared with the respective data for i.v. administration.

Comparison of the kinetics of sodium meclofenamate versus meclofenamic acid after oral administration to sheep.

Meclofenamates are non-steroidal anti-inflammatory agents used in ruminants for the prevention and the treatment of anaphylactic processes. The objective of the present work was to study possible kinetic variations due to the chemical form of meclofenamates administered by the oral route to adult sheep. Six Rubia del Molar female sheep (2-3 years old, 47-57 kg) were used. Initially, an intravenous administration of sodium meclofenamate (2.2 mg/kg bwt) was given; the obtained kinetic results were in agreement with data from other authors. Oral administrations (20 mg/kg bwt) of sodium meclofenamate and meclofenamic acid were then given. When the reticular groove was opened, both drug forms showed a single meclofenamate plasma peak; t2max were 60.0 +/- 10.61 min and 127.50 +/- 22.5 min for the sodium and acid form, respectively. The elimination rate constants (beta) were not significantly different, but the absorption half-lives were (14.69 +/- 3.21 min for the sodium form and 61.07 +/- 21.7 min for the acid form). The bioavailability was 48.6 +/- 4.3% for sodium meclofenamate and 65.1 +/- 2.8% for meclofenamic acid. Thus, the chemical form (sodium versus acid) alters the oral bioavailability and tmax of meclofenamates in adult sheep. These findings agree with the behaviour of meclofenamates in man.

Effects of verapamil, sodium nitroprusside, tetrodotoxin and caffeine on the electrical transmural stimulation induced contraction in the reticular groove smooth muscle of adult cattle.

The effect of electrical transmural stimulation (ETS) on smooth muscle strips in the floor of reticular groove of adult cattle was studied. The mechanical activity of the muscle strips was recorded isometrically. ETS (4 ms, 5 s, supramaximal voltage) caused frequency dependent (2-30 Hz) contractions of this smooth muscle. An increase in cytoplasmatic free calcium concentration can be achieved by release of the cation from intracellular store sites or by an influx of extracellular Ca2+ through calcium channels. The contractile response of the muscle strips was inhibited about 66% when it was incubated in a calcium-free EGTA-containing solution. The excitatory effect of ETS was not antagonized by verapamil (10(-6) mol/l), sodium nitroprusside (10(-6) mol/l) or tetrodotoxin (10(-6) mol/l). The electrically-evoked contraction was inhibited strongly (92%) by caffeine (30 mmol/l). The contractions of the smooth muscle from the reticular groove smooth muscle are dependent on the concentration of free calcium in the cell cytosol. This response was intracellular Ca2+ ion dependent.