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1.
The effect of dietary chloride content (0·2, 0·4 and 1·3 per cent chloride on a dry matter basis) on the disposition of a single oral dose of bromide (14 mg kg−1 was evaluated in normal beagles. Increasing the dietary chloride content from 0·2 to 1·3 per cent resulted in a significant decrease in the mean apparent elimination half-life from 69 ± 22 days to 24 ± 7 days. The mean area under the concentration curve ( ) for dogs fed 1·3 per cent chloride was significantly smaller than the for dogs fed 0·2 per cent chloride. Dietary chloride had no effect on the maximum serum concentrations (Cmax) or on the time (Tmax) to reach the maximum concentrations. The steady-state serum bromide concentrations predicted from the single dose data for daily doses of 14 mg kg−1 of bromide were significantly lower in dogs fed 1·3 per cent chloride (310 ± 150 mg litre−1) than in dogs fed 0·2 per cent chloride (1950 ± 1140 mg litre−1). The predicted mean daily doses of bromide necessary to maintain serum levels within the therapeutic range for dogs fed 1·3 per cent chloride (43 ± 13 mg kg−1) were almost twice as high as the dose estimated for dogs fed 0·4 per cent chloride (22 ± 3 mg kg−1) and nearly three times as high as the dose estimated for dogs fed 0·2 per cent chloride (15 ± 4 mg kg−l). These differences were statistically significant (P=0·002).  相似文献   

2.
The influence of methimazole on the plasma disposition kinetics of fenbendazole, oxfendazole and their metabolites, was investigated in adult sheep. The two anthelmintics were administered by oral drench at 5 mg kg−1 either alone (control treatments) or together with methimazole given orally at 3 mg kg−1. Blood samples were taken serially for 144 hours. Fenbendazole parent drug and its sulphoxide and sulphone metabolites were the three analytes observed by high performance liquid chromatography ( ) after the administration of both anthelmintics. The disposition of each analyte followed a similar pattern after the administration of the two anthehnintics alone. Oxfendazole was the main component recovered in plasma between four and 120 to 144 hours after the administration of both anthelmintics either with or without methimazole. A modified pattern of disposition, with significantly higher Cmax and values for fenbendazole parent drug, and a delayed appearance in plasma with retarded Tmax values for the sulphoxide and sulphone metabolites, were the main pharmacokinetic changes observed when the drugs were administered with methimazole.  相似文献   

3.
The pharmacokinetics of orphenadrine (ORPH) following a single intravenous (i.v.) dose was investigated in six camels (Camelus dormedarius). Orphenadrine was extracted from the plasma using a simple sensitive liquid–liquid extraction method and determined by gas chromatography/mass spectrometry (GC/MS). Following i.v. administration plasma concentrations of ORPH decline bi-exponentially with distribution half-life (t1/2α) of 0.50 ± 0.07 h, elimination half-life (t1/2β) of 3.57 ± 0.55 h, area under the time concentration curve (AUC) of 1.03 ± 0.10 g/h l−1. The volume of distribution at steady state (Vdss) 1.92 ± 0.22 l kg−1, volume of the central compartment of the two compartment pharmacokinetic model (Vc) 0.87 ± 0.09 l kg−1, and total body clearance (ClT) of 0.60 ± 0.09 l/h kg−1. Three orphenadrine metabolites were identified in urine samples of camels. The first metabolite N-desmethyl-orphenadrine resulted from N-dealkylation of ORPH with molecular ion m/z 255. The second N,N-didesmethyl-orphenadrine, resulted from N-didesmethylation with molecular ion m/z 241. The third metabolite, hydroxyl-orphenadrine, resulted from the hydroxylation of ORPH with molecular ion m/z 285. ORPH and its metabolites in camel were extensively eliminated in conjugated form. ORPH remains detectable in camel urine for three days after i.v. administration of a single dose of 350 mg orphenadrine aspartate.  相似文献   

4.
The influence of training on blood lactate concentrations during treadmill exercise and a 40-minute inactive recovery period was examined in seven trained and seven detrained thorough-bred horses. Lactate concentrations were measured in venous blood collected at the end of each exercise state, and at intervals for 40 minutes afterwards. Measurements were made of maximum oxygen uptake (V̇O2max, ml kg−1 min−1), VLA4 (velocity at which blood lactate concentration was 4 mmol litre−1); LA8 (lactate concentration [mmol litre−1] during exercise at 8 m sec−1), peak lactate (highest lactate concentration after exercise), LA40 (lactate concentration 40 minutes after exercise), the time of peak lactate concentration (minutes after exercise) and the rate of disappearance of blood lactate (Rtd). The trained horses had a significantly lower LA8 (2·1 ± 0·1 vs 6·5 ± 1 mmol litre−1, P<0·01), higher VLA4 (9·8 ± 0·2 vs 5·8 ± 0·6 m sec−1, P<0·01) and higher V̇02max (156·3 ± 3·8 vs 107·1 ± 3·9 ml kg−1 min−1, P<0·001). The value of Rtd and the time of peak lactate concentration were not significantly different.  相似文献   

5.
The study aimed to evaluate the effect of feeding Borrena hirticulata (BH), Ficus hirta (FH), rice straw (RS) and concentrate-based total mixed ration (TMR) on nutrient utilization, rumen fermentation and growth in mithun. Growing male mithun calves were randomly allotted to 2 feeding groups (6 in each), TMR1 and TMR2. The TMRs consisted of RS 300 g kg− 1, concentrate 400 g kg− 1 and BH 300 g kg− 1 (TMR1) or FH 300 g kg− 1 (TMR2) on a dry matter (DM) basis. Both TMRs were fed ad libitum to the animals for 121 d and a digestibility study was conducted during the last 7 d of the experiment. To assess rumen fermentation, rumen fluid was collected at 2 h interval for 24 h. Apparent digestibility of DM, crude protein (CP) and crude fibre (CF) did not differ significantly between the TMRs. Nevertheless, apparent digestibility of ether extract was found to be significantly (P < 0.01) greater in TMR2 (0.59) compared to TMR1 (0.54). Body weight gain (BWG; g d− 1), DM intake (kg d− 1), CP intake (g d− 1) and feed efficiency (kg feed kg− 1 gain) were found to be significantly (P < 0.05) greater in TMR1 (548, 5.14, 713 and 9.28) compared to TMR2 (496, 4.91, 703 and 10.03). An insignificant positive association (r = 0.35) between DM intake and BWG, but a significant (P < 0.01) positive association (r = 0.74) between CP intake and BWG were evident. Rumen pH (5.71 to 7.18) and ammonia-nitrogen (8.0 to 25.0 mg/dl) did not differ significantly between the TMRs, but differed significantly (P < 0.01) at different h post-feeding. In contrast, rumen total volatile fatty acid (42 to 105 mM) and total nitrogen (40.4 to 90.3 mg/dl) differed significantly (P < 0.05) between the TMRs and at different h post-feeding. The study revealed that BH, FH, RS and concentrate-based TMRs may be fed to mithun for satisfactory growth.  相似文献   

6.
The rate of reversal of neuromuscular block was compared in 36 sheep receiving either edrophonium (500 μg kg−1) and atropine (80 μg kg−1), neostigmine (50 μg kg−1) and atropine (80 μg kg−1) or saline (10 ml), using the train of four count (TO4C) recorded at n. facialis - m. levator nasolabialis. Neuromuscular block was produced with mivacurium (200 μg kg−1) followed later by a single incremental dose of 70 μg kg−1. Antagonists or saline were given when spontaneous recovery from the incremental dose (T04C = 1) = 1 begun. The T04C increased from 1 to 4 in all animals, in all treatment groups within 10 minutes of reversal. The T04C was 4 in all animals five minutes after edrophonium, and seven minutes after neostigmine; differences were not statistically significant. The T04C was significantly higher with edrophonium two and three minutes after antagonism compared with saline. The data show that spontaneous recovery from mivacurium is rapid in sheep, although reversal is accelerated by anticholinesterase drugs.  相似文献   

7.
Five days after the induction of acute systemic inflammation in greyhounds by intramuscular and subcutaneous injections of Freund's adjuvant, the hepatic concentrations of cytochromes P-450 and b5, the activities of the hepatic microsomal enzymes aniline p-hydroxylase and aminopyrine n-demethylase and the disposition and urinary excretion of phenylbutazone were determined. The mean plasma concentrations of phenylbutazone after intravenous administration were described by the bi-exponential equations: Cp = 144·2e−34·6t + 171·5e−0·104t for five normal greyhounds and Cp = 113·6e−16·13t + 163·1e−0·108t for five febrile greyhounds. The elimination half-lives, total body clearances and apparent volumes of distribution were 6·7 hours, 18·4 ml kg−1 hour−1 and 0·18 litre kg−1, for the normal greyhounds, and 6·4 hours, 19·5 ml kg−1 hour−1 and 0·18 litre kg−1, for the febrile greyhounds. There were no significant differences between the pharmacokinetic parameters describing the distribution and elimination of phenylbutazone, or between the quantities of phenylbutazone, oxyphenbutazone and hydroxyphenylbutazone excreted in the urine. In the febrile greyhounds, there were significant decreases in the hepatic microsomal concentrations of cytochromes P-450 and b5 and in the activities of aniline p-hydroxylase and aminopyrine n-demethylase.  相似文献   

8.
In an open, controlled, multi-centre clinical field trial, seven ‘naturally occurring’ outbreaks of acutefebrile (rectal temperature ≥ 39·5°C) respiratory disease in housed calves were treated with a single antimicrobial agent, and either the non-steroidal anti-inflammatory drug (NSAID) carprofen (n=95) or flunixin meghunine (n=92) on an alternate basis. Carprofen was administered as a single subcutaneous injection at a mean dosage of 1·4 mg kg−1 (range 1·2 to 1·9 mg kg−1) body weight on the first day and flunixin meglumine by intravenous injection at a mean dosage of 2·0 mg kg−1 (range 1·2 to 2·6 mg kg−1) body weight on the first 3 consecutive days. All calves were examined clinically immediately prior to initial treatment and on three occasions up to 1 week after the end of treatment. There were no statistically significant differences between NSAID groups in reduction of clinical parameters between examinations, or in overall efficacy. This trial demonstrated that a single dose of carprofen was equally effective as three daily closes of flunixin meglumine as adjunctive therapy to antimicrobial treatment in acute respiratory disease in calves.  相似文献   

9.
The aim of the present study was to investigate the effects of intravenously administered sulfadoxine (5 mg kg −1 bodyweight) or sulfaphenazole (5 mg kg−1 bodyweight) on the in vivo elimination of i.v. tolbutamide (5 mg kg−1 bodyweight), as both compounds were shown to inhibit tolbutamide hydroxylation in vitro. It was shown that relative large differences in tolbutamide clearance exist among goats (n = 6). A high correlation was seen between tolbutamide and sulfadoxine clearances. Tolbutamide clearance was significantly reduced by concommitant administration of sulfaphenazole. Sulfadoxine ( ) had a less consistent effect. Mean tolbutamide plasma clearance was not significantly affected due to the fact that three animals showed an inhibition, whereas three others apparently did not respond. A negative correlation was found between the amount of N4-acetyl in urine and the clearance. Approximately 93 per cent of tolbutamide was bound to plasma proteins. However, there was no evidence for displacement of tolbutamide from its protein binding sites by sulfaphenazole or sulfadoxine. The results described in the present study confirm previous in vitro data obtained with goat hepatocytes. Although quantitative differences in inhibition exist between in vivo and in vitro results, hepatocytes are a good model to study potential drug-drug interactions at the level of biotransformation processes.  相似文献   

10.
The effects of feeding diets with different milliequivalents (mEq) of dietary ([Na+ + K+] − [Cl− + SO4=]) to dairy cows during the last seven weeks of pregnancy on bone morphology at parturition were studied. Nine monozygotic twin pairs of pregnant cows (five pairs of parity 1 or 2 and four pairs of parity 3 or more) were allocated to two diets which were formulated to provide either −4 mEq (anion diet) or +572·5 mEq (cation diet) of ([Na+ + K+] − [Cl− + SO4=]) kg−1 dietary dry matter. Bone biopsies were taken from the tuber coxae between three and eight hours after parturition. The plasma concentrations of calcium and inorganic phosphorus, the total plasma alkaline phosphatase activity and the urinary hydroxyproline:creatinine ratio were not significantly affected by diet during the experimental period. In low parity (2 or less) cows the percentage trabecular bone volume, the percentage osteoclast surface and the mean number of osteoclasts per microscopic field (identified by Goldner staining) were lower on the anion diet than on the cation diet (P<0-02). In the high parity cows, the percentage osteoid volume (P<0·05) and the ratio of percentage osteoid volume to percentage osteoid surface (P<0·001) were greater in the cows fed the anion diet than in the cows fed the cation diet. The results show that reducing the mEq of dietary ([Na+ + K+] − [Cl− + SO4=]) to −4 mEq kg−1 dietary dry matter affected some of the parameters of bone formation but did not enhance bone resorption.  相似文献   

11.
The pharmokinetic properties of amoxycillin, and its penetration into respiratory tract tissue, were determined in 18 Actinobacillus pleuropneumoniae infected pigs, after a single i.v. dose of 8·6 mg amoxycillin kg−1 bodyweight. Pleuropneumoniae was produced experimentally in pigs by an aerosol infection model. The infection created a homogenous response, characterised by depression of breathing and increased body temperature. The clinical symptoms were accompanied by increased haptoglobin levels and circulating white blood cell counts. At necropsy the findings were characterised by a bilateral fibrinous pleuropneumonia. Twenty hours after infection, the pigs were administered amoxycillin i.v. The plasma concentration-time curve was described by a three compartment open model. The mean residence time and the elimination half-life were l·5 and 3·4 hours, respectively. The steady-state volume of distribution was 0·67 litres kgl, and the clearance was 0·46 litres kg−1 hour−1. There were no significant differences between these values and those reported previously for healthy pigs. The concentration of amoxycillin in bronchial secretions, lung tissue and diseased lung tissue peaked two hours after intravenous drug administration, while amoxycillin concentration in pleural fluid, lymph nodes and tonsil tissue peaked at the first sampling point one hour after drug administration. The concentration of amoxycillin in secretions and tissue decreased by a slower rate than amoxycillin concentration in plasma, resulting in an increasing tissue-to-plasma concentration ratio. The distribution ratios (AUCtissue/JAUCplasma) was 0·53 for bronchial secretions, 0·44 for pneumonic lung tissue, 0·42 for lung tissue, 1·04 for pleural fluid, 0·58 for lymph nodes and 0·37 for tonsil tissue. The distribution of amoxycillin to secretions was increased compared with that previously reported for healthy pigs, while only minor changes were observed in lung tissue.  相似文献   

12.
The single-dose disposition kinetics of marbofloxacin (MBX) were determined in clinically healthy loggerhead sea turtles (n = 5) after oral (PO) administration of 2 mg kg−1 bodyweight. Marbofloxacin plasma concentrations were determined by DAD–HPLC (LOD/LOQ 0.015/0.05 μg ml−1). Data were subjected to non-compartmental analysis. Following PO administration, marbofloxacin achieved maximum plasma concentrations of 11.66 ± 2.53 mg L−1 at 15.00 ± 3.00 h. The absence of general adverse reactions in the turtles of the study, and the favourable pharmacokinetic properties (long half-life and high maximum plasma concentration) of MBX administered PO at the single-dose of 2 mg kg−1 suggest the possibility of its safe and effective clinical use in loggerhead sea turtles.  相似文献   

13.
Fluconazole (100 mg) was administered to six adult cats as an intravenous infusion over 30 minutes, and the same cats received 100 mg of the drug orally 16 weeks later. The cats were bled repeatedly through an indwelling jugular catheter, the plasma fluconazole concentrations were assayed by high performance liquid chromatography, and the concentration-time data were subjected to a non-compartmental pharmacokinetic analysis. The mean (SD) intravenous half-life (13·8 [2·6] hours) was similar to that observed after oral dosing (12·4 [3·0] hours). The plasma clearances (intravenous 0·9 [0·1], oral 0·9 [0·2] ml min−1 kg−1) and the volumes of distribution at steady state (intravenous 1·1 [0·1], oral 1·0 [0·1] litre kg−1) were also similar after the two routes of dosing. The peak plasma concentration was reached 2·6 hours after oral dosing and the drug was completely bioavailable (1·09 [0·05]). On the basis of this single dose study, the administration of 50 mg fluconazole every eight hours to a 4 kg cat should produce average steady state plasma fluconazole concentrations of approximately 33 mg litre−1.  相似文献   

14.
Intravenous infusions of hydrocortisone sodium succinate (HSS) were given at 0·625 mg kg−1 hour−1 and 0·312 mg kg−1 hour−1 to six dogs. Plasma cortisol concentrations were measured by radioimmunoassay at 0, 15, 30, 45 and 60 minutes and then every 30 minutes for a further five hours. Chronic hypocortisolaemia was induced and maintained with mitotane and the HSS infusions were repeated after 31 and 50 days. No statistically significant difference was observed in the plasma cortisol concentrations after either period of hypocortisolaemia, but the plasma cortisol concentrations tended to be higher in most of the dogs.  相似文献   

15.
Ureaplasma species were isolated from semen samples collected sequentially from one Awassi and three Assaf breeding rams. Each ram was injected subcutaneously with an aqueous solution of lincomycin and spectinomycin for five consecutive days at a dose equivalent to 4·5 mg kg−1 lincomycin and 9·0 mg kg−1 spectinomycin daily. Serum and semen samples were collected at intervals during the treatment and assayed for lincomycin. No Ureaplasma species were isolated from semen samples collected during the course of the treatment and at intervals for 17 days after the last treatment. The concentration of lincomycin in semen ranged from 0·51 μg ml−1 four hours after treatment to 0·08 μg ml−1 24 hours after treatment, and these levels were three to nine times higher than the corresponding serum concentrations.  相似文献   

16.
Blood acid-base and electrolyte status was studied in four sedentary Miniature Horses treated with 200, 300, 400 and 500 mg of sodium bicarbonate (NaHCO3) per kg of body weight (BW). Arterial blood was collected before treatment with NaHC03 and each hour for 5 h after treatment. All treatments resulted in an increase in blood pH, bicarbonate (HCO3−) concentration and base excess (BE) by 1 h post-dosage, which continued through the 5th hour (P < .05). Treatment with 200 mg NaHC03/kg BW resulted in less elevated blood HCO3− concentrations (P < .03) and BE values (P < .01) when compared to the other treatments. Following dosing with NaHCO3, plasma Na+ concentrations increased among all treatments but declined to initial values by 3 h post-treatment. The 200 mg NaHCO3/kg BW dosage resulted in the smallest increases in plasma Na+ concentrations (P < .03). Both plasma K+ and Ca++ concentrations were lower (P < .05) among all treatment groups 1 h post-dosage but returned to initial values by 5 h and 3 h posttreatment, respectively, with no differences (P >.05) among treatments. All NaHCO3 dosages increased blood buffering capacity as indicated by increased blood pH, HCO3− concentration and BE. Maximum blood pH, HCO−3 concentration and BE was reached using a dosage of 300 mg NaHCO3/kg BW. Also, all treatments altered the plasma electrolyte concentrations.  相似文献   

17.
To evaluate the effects of dietary supplementation with a marine algae product (MA) containing a high level of docosahexaenoic acid (DHA) on heavy pig production performances (including meat and subcutaneous fat quality), a trial was conducted on sixty Landrace × Large White barrows with a starting average body weight (BW) of 118 kg. Pigs were allocated to four experimental groups: a control group (A) fed a maize/soybean diet and three treatment groups in which MA was added at 2.5 g kg− 1 over the last 8 weeks prior to slaughtering (group B) or at 5 and 2.5 g kg− 1 over the last 4 weeks prior to slaughtering (groups C and D, respectively). Vitamin E was added at 12.5 mg kg− 1 in the diets for groups B and D and at 25 mg kg− 1 in the diet of group C. The four diets were formulated so as to supply the same amount of nutrients, with exception of vitamin E. Pigs were fed at a rate of 9% of their metabolic BW (BW0.75) up to a maximum of 2.9 kg of dry matter per pig per day. Pigs were slaughtered at about 160 kg BW. The dietary treatment did not affect either the growth or slaughtering parameters of pigs. No significant differences were observed with respect to pH values, meat colour, loin composition and the iodine number of subcutaneous fat. Pigs on MA diets showed a significant (P < 0.01) improvement in DHA levels both in loin and in subcutaneous fat. No significant differences in relative fatty acid composition were observed between pigs receiving the MA supplement at the lower level (2.5 g kg− 1) over an 8-week period (group B) and pigs receiving the higher MA supplement (5.0 g kg− 1) over a 4-week period prior to slaughter (group C).  相似文献   

18.
In this study, supplementation of two levels (5 and 25 parts per million; ppm) of boron into broiler diets including 125 kg−1(inadequate) and 2000 kg−1(adequate) vitamin D3as investigated. The effects of supplementation on performance and biochemical characters (Ca, P, Mg, glucose and ) of broilers from 1 to 45 days of age were evaluated. Boron provided significant increases in performances of chicks fed both adequate and inadequate vitamin D3-containing diets. The improvements in the inadequate vitamin D3-containing group were higher than that of adequate vitamin D3-containing group. The boron addition had a positive effect on Ca, P and alkaline phosphatase levels of chicks. Boron might be regarded as beneficial in inadequate vitamin D3-containing broiler feed.  相似文献   

19.
During oestrous cycles of the camel, spontaneous uterine contractions were correlated significantly with plasma oestradiol-17β concentration. Ovariectomy in the camel resulted in a decreased plasma concentration of oestradiol-17β (<15 pg ml−1) and progesterone (<0·1 ng ml−1) and caused complete cessation of uterine activity. Daily administration of oestradiol benzoate (5 mg, intramuscularly) increased the plasma concentration of oestradiol-17β (>45 pg ml−1) and increased the frequency and amplitude of uterine activity. Coadministration of progesterone (100 mg, intramuscularly) increased the plasma concentration of progesterone (>4 ng ml−1) and increased the frequency but not amplitude of uterine activity. It is suggested that uterine activity in the camel is correlated with the circulating levels of oestradiol-17β and progesterone.  相似文献   

20.
The effects of cholecystokinin-8 (cck-8) and pentagastrin on insulin and glucagon secretion were studied in conscious sheep. Intravenous infusions of ccx-8 (3 to 1000 pmol kg−1 min−1 for 30 minutes) induced a dose-dependent increase in plasma insulin, but did not alter plasma glucagon concentration. The threshold dose of ccx-8 for stimulation of insulin secretion was 10 to 30 pmol kg−1 min−1. Pentagastrin was infused intravenously at doses of 10 to 3000 pmol kg−1 min−1. The maximal dose of pentagastrin slightly stimulated insulin, but not glucagon, secretion. The insulin secretory activity of pentagastrin was only 1/300 that of ccx-8 on a molar basis. The threshold dose of ccx-8 for stimulation of insulin secretion was similar to that for exocrine pancreatic secretion obtained in earlier studies. In conclusion, ccx is a potential candidate as a physiological factor regulating insulin secretion in sheep.  相似文献   

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