scholarly journals Pharmacokinetics and Bioavailability of Carprofen in Rainbow Trout (Oncorhynchus mykiss) Broodstock

Pharmaceutics ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 990
Author(s):  
Kamil Uney ◽  
Duygu Durna Corum ◽  
Ertugrul Terzi ◽  
Orhan Corum
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
High Performance ◽  
Peak Plasma ◽  
Peak Plasma Concentration ◽  
Plasma Concentrations ◽  
Compartmental Analysis ◽  
Oral Route ◽  
Pharmacokinetic Parameters ◽  
Rainbow Trout Oncorhynchus Mykiss

The aim of this study was to determine the pharmacokinetics of carprofen following intravenous (IV), intramuscular (IM) and oral routes to rainbow trout (Oncorhynchus mykiss) broodstock at temperatures of 10 ± 1.5 °C. In this study, thirty-six healthy rainbow trout broodstock (body weight, 1.45 ± 0.30 kg) were used. The plasma concentrations of carprofen were determined using high-performance liquid chromatography and pharmacokinetic parameters were calculated using non-compartmental analysis. Carprofen was measured up to 192 h for IV route and 240 h for IM, and oral routes in plasma. The elimination half-life (t1/2λz) was 30.66, 46.11, and 41.08 h for IV, IM and oral routes, respectively. Carprofen for the IV route showed the total clearance of 0.02 L/h/kg and volume of distribution at steady state of 0.60 L/kg. For IM and oral routes, the peak plasma concentration (Cmax) was 3.96 and 2.52 μg/mL with the time to reach Cmax of 2 and 4 h, respectively. The bioavailability was 121.89% for IM route and 78.66% for oral route. The favorable pharmacokinetic properties such as the good bioavailability and long t1/2λz for IM and oral route of carprofen suggest the possibility of its effective use for the treatment of various conditions in broodstock.

Comparative Pharmacokinetics and Bioavailability of Oxolinic Acid in Channel Catfish (Ictalurus punctatus) and Rainbow Trout (Oncorhynchus mykiss)

1994 ◽  
Vol 51 (5) ◽  
pp. 1205-1211 ◽  
Author(s):  
Kevin M. Kleinow ◽  
Herman H. Jarboe ◽  
Kathy E. Shoemaker ◽  
Kevin J. Greenless
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Ictalurus Punctatus ◽  
Channel Catfish ◽  
Plasma Concentrations ◽  
Oxolinic Acid ◽  
Distribution Data ◽  
Antibacterial Drug ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Elimination Half

The pharmacokinetics, bioavailability, and disposition of oxolinic acid (OA), a quinolone antibacterial drug, were examined in a warmwater (channel catfish (Ictalurus punctatus)) and coldwater fish species (rainbow trout (Oncorhynchus mykiss)). Studies were performed at 24 and 14 °C for catfish and at 14 °C for trout to compare temperature- and species-related differences. Analysis of OA pharmacokinetics when determined by HPLC provided elimination half-life [Formula: see text], volume of distribution (Vss), and clearance (Clb) estimates for 24 °C catfish, 14 °C catfish, and 14 °C trout of 40.9, 69.3, and 81.3 h, 939, 880, and 1817 mL/kg, and 16.3, 8.9, and 16.9 mL∙kg∙h−1, respectively. Following oral administration, OA plasma concentrations peaked between 8 and 24 h for all treatments; however, 14 °C trout and 14 °C catfish sustained peak concentrations for a longer duration than 24 °C catfish. Oral OA bioavailabilities were 56.0, 91.8, and 90.7% for 24 °C catfish, 14 °C catfish, and 14 °C trout, respectively. OA distribution data for muscle of 14 °C catfish demonstrated an inordinately high peak concentration and delayed time to peak relative to other treatments. Elimination half-lives of OA in muscle were 33.1, 54.3, and 141 h for 24 °C catfish, 14 °C catfish, and 14 °C trout, respectively.

Effects of stress on plasma homeostasis, endolymph chemistry, and check formation during otolith growth in rainbow trout (Oncorhynchus mykiss)

2004 ◽  
Vol 61 (7) ◽  
pp. 1247-1255 ◽  
Author(s):  
P Payan ◽  
H De Pontual ◽  
A Edeyer ◽  
G Borelli ◽  
G Boeuf ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Plasma Concentrations ◽  
Growth Stress ◽  
Significant Rise ◽  
External Stress ◽  
Otolith Growth ◽  
Ph Variation ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Different Levels

This is the first study in which the effects of an external stress were analysed at different levels: plasma ho meostasis, endolymph chemistry, and otolith growth. Stress was applied to rainbow trout (Oncorhynchus mykiss) by exposure to Cl2 gas. In the plasma of Cl2-stressed trout, Na+ and Cl– decreased (70 mmol·L–1) and K+ increased (2.0 mmol·L–1), whereas total Ca was unchanged. A slight hypercapny (+2.4 mmHg (1 mmHg = 133.322 Pa)) was observed related to a significant rise (40%) in total CO2 without pH variation. In the endolymph, Na+ and Cl– also decreased, whereas other parameters (K+, PO43–, Mg, and, peculiarly, total Ca) remained stable. The important effect provoked by Cl2 stress in endolymph was an increase of proteins (factor of 2.6) and total CO2 (factor of 3.1) concentrations at the proximal side of the endolymph. The stress induced a decrease in otolith growth rate and produced a discontinuity (check) in the microstructure pattern of the otolith characterized by a large D zone. The variations in the endolymph composition are discussed and we propose that they result not only from changes in plasma concentrations, but also from changes (organic and crystallization) in otolith deposition.

Protective effects of calcium against the physiological effects of exposure to a combination of cadmium and copper in rainbow trout (Oncorhynchus mykiss)

1999 ◽  
Vol 77 (7) ◽  
pp. 1035-1047 ◽  
Author(s):  
Jeff G Richards ◽  
Richard C Playle
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Plasma Concentrations ◽  
Lactate Concentration ◽  
Haemoglobin Concentration ◽  
Arterial Oxygen Tension ◽  
Soft Water ◽  
Arterial Oxygen ◽  
Cd Accumulation ◽  
Rainbow Trout Oncorhynchus Mykiss

We report that an elevated aqueous calcium (Ca) concentration protects against acute respiratory and osmoregulatory action due to exposure to a combination of cadmium (Cd) and copper (Cu) in rainbow trout (Oncorhynchus mykiss), but does not protect against longer term ionoregulatory disruption. Trout exposed to 0.18 µM Cd and 0.80 µM Cu in soft water (40 µM Ca, 440 µM Na, pH 6.6) experienced a 60-torr decrease in arterial oxygen tension, a 5.5 mM increase in blood lactate concentration, and severe haemoconcentration as indicated by a 1.4-fold decrease in mean cell haemoglobin concentration, all of which occurred within 24 h. The addition of Ca to soft water (to reach 910 µM Ca, added as CaCl2; 430 µM Na, pH 6.8) eliminated these severe effects and slowed Cd uptake by the gills, plasma, and liver of trout, probably through competition for binding at gill Ca channels, but Ca did not affect Cu uptake by the gills or its entry into the plasma. Associated with slower Cd accumulation and unchanged Cu accumulation in the plasma were slow decreases in plasma concentrations of Na, Cl, and Ca, which were prevented initially by adding Ca to the water. Modelling using a modified aqueous chemistry computer program, MINEQL+, and previously published gill binding constants accurately simulated the initial (18 h) accumulation of Cd and Cu by trout gills and thus predicted acute toxicity, but our model did not adequately simulate the physiological mechanisms of Cd accumulation by trout gills over longer exposures up to 130 h.

scholarly journals Pharmacokinetic Study of Human Immunodeficiency Virus Protease Inhibitors Used in Combination with Amprenavir

2001 ◽  
Vol 45 (12) ◽  
pp. 3663-3668 ◽  
Author(s):  
Brian M. Sadler ◽  
Catherine Gillotin ◽  
Yu Lou ◽  
Joseph J. Eron ◽  
William Lang ◽  
...  
Keyword(s):  
Human Immunodeficiency Virus ◽  
Steady State ◽  
Protease Inhibitors ◽  
Pharmacokinetic Study ◽  
Peak Plasma ◽  
Peak Plasma Concentration ◽  
Plasma Concentrations ◽  
Pharmacokinetic Parameters ◽  
Open Label ◽  
Immunodeficiency Virus

ABSTRACT In an open-label, randomized, multicenter, multiple-dose pharmacokinetic study, we determined the steady-state pharmacokinetics of amprenavir with and without coadministration of indinavir, nelfinavir, or saquinavir soft gel formulation in 31 human immunodeficiency virus type 1-infected subjects. The results indicated that amprenavir plasma concentrations were decreased by saquinavir soft gel capsule (by 32% for area under the concentration-time curve at steady state [AUCss] and 37% for peak plasma concentration at steady state [C max,ss]) and increased by indinavir (33% for AUCss). Nelfinavir significantly increased amprenavir minimum drug concentration at steady state (by 189%) but did not affect amprenavir AUCss orC max,ss. Nelfinavir and saquinavir steady-state pharmacokinetics were unchanged by coadministration with amprenavir compared with the historical monotherapy data. Concentrations of indinavir, coadministered with amprenavir, in plasma decreased in both single-dose and steady-state evaluations. The changes in amprenavir steady-state pharmacokinetic parameters, relative to those for amprenavir alone, were not consistent among protease inhibitors, nor were the changes consistent with potential interactions in CYP3A4 metabolism or P-glycoprotein transport. No dose adjustment of either protease inhibitor in any of the combinations studied is needed.

Natural and commercial dissolved organic matter protects against the physiological effects of a combined cadmium and copper exposure on rainbow trout (Oncorhynchus mykiss)

1999 ◽  
Vol 56 (3) ◽  
pp. 407-418 ◽  
Author(s):  
Jeff G Richards ◽  
B Kent Burnison ◽  
Richard C Playle
Keyword(s):  
Organic Matter ◽  
Rainbow Trout ◽  
Dissolved Organic Matter ◽  
Oncorhynchus Mykiss ◽  
Computer Modelling ◽  
Plasma Concentrations ◽  
Binding Constants ◽  
Physiological Effects ◽  
Copper Exposure ◽  
Rainbow Trout Oncorhynchus Mykiss

Environmentally realistic concentrations of a natural dissolved organic matter (DOM) (8 mg C/L as dissolved organic carbon (DOC)) protected against the acute respiratory and ionoregulatory effects of 0.2 µM Cd and 0.8 µM Cu on rainbow trout (Oncorhynchus mykiss). The protection afforded by low natural DOC was the same as that afforded by similar or higher concentrations of commercial DOC. Trout exposed to the metals alone experienced large decreases in arterial PO2, increases in arterial PCO2, increases in blood lactate, decreases in plasma concentrations of Cl, and developed pronounced haemoconcentration. There were no deleterious effects of 31 mg C/L commercial DOC on any measured aspect of trout physiology except for an increase in plasma Cl, which was probably due to elevated aqueous Cl concentrations associated with the DOM addition. No concentration of DOC used in the present study prevented Cd from being bound by trout gills, and some of these fish showed hypocalcemia; however, Cu was kept off the gills of trout exposed to metals plus DOM. Computer modelling using metal-gill binding constants simulated well the accumulation of Cd and the lack of Cu accumulation by trout gills in the presence of DOM.

scholarly journals Accumulation of arsenic during the growing period of rainbow trout (Oncorhynchus mykiss)

2011 ◽  
Vol 80 (2) ◽  
pp. 219-225 ◽  
Author(s):  
Olga Čelechovská ◽  
Veronika Harkabusová ◽  
Blanka Macharáčková ◽  
Eva Vitoulová ◽  
Alena Lavičková
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
High Performance ◽  
Atomic Fluorescence Spectrometry ◽  
Processing Plant ◽  
Total Arsenic ◽  
Running Water ◽  
Growing Period ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Significant Difference

Rainbow trout (Oncorhynchus mykiss) was monitored for the duration of one year, from 2 to 14 months of age (n = 120). The study was performed on a farm with through-running water from the basin of water processing plant in the years 2007 and 2008. During the first months of fish life, we analyzed homogenized samples (n = 12) of rainbow trout bodies. From the 8th month the samples of twelve rainbow trouts were analysed. The total contents of arsenic and arsenobetaine were quantified in muscle, liver, spleen and bile separately. The total arsenic was determined by hydride technique AAS and arsenobetaine by high performance liquid chromatography combined with detection using atomic fluorescence spectrometry. The concentration of arsenic in homogenized body samples grew (P < 0.01) during the first months of life, from the 6th month of rearing no significant difference was found. The concentration of arsenobetaine in homogenized bodies was low during the first months and from the 6th month the concentration stayed on invariable level and amounted to 46 ± 6% of total arsenic. The highest concentrations of arsenic and arsenobetaine in tissues ranked in the order muscle, liver, spleen and bile. In summer months the total arsenic in muscle was bonded in the form of arsenobetaine, in winter months the content of arsenobetaine dropped to 50% of total arsenic. The content of arsenic in liver samples remained the same during the entire monitoring, however, the ratio of arsenobetaine content altered. In summer months it reached the maximum 27%, in winter months it dropped to 7% of arsenic. The concentration of arsenic in spleen and bile decreased in winter months, arsenobetaine corresponded to the value assessed in liver. This study proved the effect of the small content of arsenic in feedstuff on accumulation of total arsenic and arsenobetaine in the tissue of rainbow trout during the growing period and season.

scholarly journals Influence of Pyrexia on Pharmacokinetics of Azithromycin and Its Interaction With Tolfenamic Acid in Goats

2021 ◽  
Vol 8 ◽  
Author(s):  
Sini Mechery ◽  
Suresh Narayanan Nair ◽  
Thirumangalath Meethal Divya ◽  
Kanjirakuzhiyil Promod ◽  
Sakkariya Ibrahim Nalukudy Paramba ◽  
...  
Keyword(s):  
High Performance ◽  
Peak Plasma ◽  
Peak Plasma Concentration ◽  
Area Under The Curve ◽  
Compartmental Analysis ◽  
Inflammatory Cells ◽  
Tolfenamic Acid ◽  
Human Beings ◽  
Moment Curve ◽  
Anti Inflammatory

Azithromycin is a macrolide antimicrobial agent of the azalide group with a broad spectrum of activity against gram-negative and gram-positive bacterial organisms. Tolfenamic acid is a non-steroidal anti-inflammatory drug of the fenamate group, which is used extensively in humans and animals due to its anti-inflammatory, analgesic, and antipyretic properties. There is dearth of literature on any type of drug interaction between azithromycin and tolfenamic acid in any species, including human beings and alteration of its pharmacokinetics by fever. Therefore, the objective of this study was to investigate the alteration of disposition kinetics of azithromycin alone and in the presence of tolfenamic acid in Malabari goats by fever, following an intravenous administration at a dose rate of 20 mg/kg body weight. Blood samples collected from both afebrile and febrile goats at predetermined time intervals after the administration of azithromycin alone and then in combination with tolfenamic acid (2 mg/kg, intravenously), respectively, were analyzed using high-performance liquid chromatography. Non-compartmental analysis was used to determine the peak blood concentration (Cmax), time-to-peak plasma concentration (Tmax), half-life (t1/2λz), area under the curve (AUC 0−t, AUC 0−inf), area under the first moment curve (AUMC 0−inf), mean residence time (MRT0−inf), apparent volume of distribution at steady state (Vss), and the total body clearance of drug from the blood (Cl). In febrile animals, significant differences were noted in the values of Cmax, Cl, and Vss. Thus, azithromycin disappears into an additional compartment in febrile goats, which may be due to its extended cellular penetration into the inflammatory cells, resulting in anti-inflammatory activity. Tolfenamic acid significantly altered the pharmacokinetics of azithromycin in both normal and febrile animals. Tolfenamic acid, being a better anti-inflammatory agent, suppresses the inflammatory mediators, reducing the possibility of increased utilization of azithromycin in febrile condition.

Plasma levels of lactate, potassium, glucose, cortisol, growth hormone and triiodo-L-thyronine in rainbow trout (Oncorhynchus mykiss) during exercise at various levels for 24 h

1994 ◽  
Vol 72 (9) ◽  
pp. 1643-1647 ◽  
Author(s):  
Michael E. Nielsen ◽  
Lars Boesgaard ◽  
Ruston M. Sweeting ◽  
Brian A. McKeown ◽  
Per Rosenkilde
Keyword(s):  
Growth Hormone ◽  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Acute Stress ◽  
Plasma Concentrations ◽  
Exercise Group ◽  
Moderate Exercise ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Lactate Levels

To examine the initial hormonal and metabolic changes in exercising fish, rainbow trout (Oncorhynchus mykiss) were subjected to moderate (1.5 body lengths/s) or low (0.5 body lengths/s) water velocities for 24 h and compared with unexercised controls. Blood sampling occurred immediately before (0 h) and at 1, 2, 4, 8, and 24 h after the onset of exercise for determination of plasma concentrations of lactate, potassium, glucose, cortisol, growth hormone, and triiodo-L-thyronine (T3). There was no effect of either exercise or time on plasma lactate levels in any of the three groups, indicating that neither exercise regime induced anaerobic conditions. Within the first 2 h of exercise, plasma, K+, glucose, cortisol, and growth hormone levels were all significantly (P < 0.05) elevated over controls in the moderate-exercise group. By 4 h, none of these parameters were significantly different from controls except plasma K+ levels, which remained significantly higher throughout the experiment. There were no differences between 0 and 24 h of exercise in any parameters of any of the groups, again with the exception of plasma K+ levels in the moderate-exercise fish, which were significantly higher at 24 h. It is concluded that the effects of the onset of exercise resemble those described for acute stress in fish. Furthermore, short-term (24 h) exercise at moderate levels (1.5 body lengths/s) resulted in continuously elevated plasma K+ levels, but did not seem to cause similar increases in the other parameters.

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