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Biomedical subjects

P Bouyard

Publications and source records attributed to P Bouyard.

At least 19 recordsLinked to original sources

[Pharmacokinetic, biochemical and histological study of the carbamazepine-josamycin interaction in the rat following chronic administration].

The determination of possible modifications of pharmacokinetic parameters of carbamazepine by josamycin in an experimental study after chronic administration of the drugs in the rat was undertaken to assay, or not, the enzymatic inhibition hypothesis which is supported in human clinical studies. Our data do not show any alteration in the Cmax, Tmax and AUC parameters of carbamazepine (total and unbound fraction) in case of conjunction with josamycin, but an earlier increase of plasmatic concentrations. The biochemical parameters are not modified, but a significant decrease of total bilirubin compared with controls and carbamazepine alone. The histological study does not show any liver lesion.

Animals↗

Sodium valproate: kinetic profile and effects on GABA levels in various brain areas of the rat.

1. The kinetic profile of sodium valproate (VPA) and the GABA levels were studied in discrete brain areas of the rat after an i.p. injection of 200 mg/kg. The results were discussed comparatively with GABA-T and GAD activities reported in the literature. 2. VPA was rapidly distributed in brain areas; its concentrations, its kinetic parameters and the GABA levels after the drug administration were not uniform in the different brain areas studied. 3. The results showed a particular relation of the VPA to the olfactory bulbs; in this specific area the VPA effect on GABA level was stronger; the VPA apparent half life of elimination was longest; the VPA apparent disappearance rate constant was smallest; the initial GABA level was higher; the activities of GABA-T and GAD were higher than in other brain areas studied except the hypothalamus. 4. These data were correlated with the role of the olfactory bulbs in the behaviour of the rodents.

Animals↗

[Neuro-endocrine effects of chronic clonidine administration in rats].

Neuroendocrine effects of chronic clonidine administration - which has been proposed as antimanic drug - have been evaluated in the female rat for a twenty one days period at the following doses : 0,5 ; 5 ; 25 and 50 micrograms.kg-1.day-1. No modification of the evolution of the oestrus cycle was observed, whereas pituitary hormones (PRL, FSH and LH) plasma levels were not statistically modified. The results of this study are opposed to those frequently observed with classical neuroleptic drugs.

Animals↗

[Absence of effects of sodium valproate on the estrous cycle of the rat].

Regarding interrelationships between epilepsy, antiepileptic drugs and neuroendocrinological events, sodium valproate effects on estrous cycle of the rat have been performed by daily vaginal smears for twenty one days with 200, 100, 20 and 10 mg per kg bodyweight. Our data showed that sodium valproate did not significantly modify the evolution of estrous cycle even if intracerebral GABA content increase has been reported to influence hormonal secretions.

Animals↗

Circadian effect on carbamazepine kinetics in rat.

The purpose of the present study was to investigate whether the time of day (24 h) at which carbamazepine is administered influences its pharmacokinetics in the rat. The pharmacokinetics of a single, 100 mg . kg-1 bodyweight per os, dose of carbamazepine were studied at four different fixed time points of a 24-hour period (i.e. 10.00, 16.00, 22.00 or 04.00 h) in Wistar AF-SPF adult male rats maintained under controlled environmental conditions (LD: 18.00 - 06.00h) during October 1978. The total plasma levels and the unbound fraction were measured according to an immunoenzymatic method (EMIT). The effects of fasting were also investigated. The data shows circadian variations of pharmacokinetic parameters: the maximum peak concentration and the maximum time to reach this peak was observed when the drug was given respectively at 16.00h and at 10.00h. The elimination half-life varied from 15.15 hours at 16.00h to 10.48 hours at 22.00h. The observed variations may be related to: daily fluctuations of absorption or binding of the drug; diurnal variations of the hepatic drug metabolizing enzymes responsible for the inactivation; and/or diurnal variations in excretion rate of the drug.

Administration, Oral↗

[Possible effects of propranolol on the estrous cycle of the rat].

Propranolol effects on oestrous cycle of the rat have been studied by daily vaginal smears for twenty one days with doses nearby similar to those used in psychiatric disorders (e.g. 3, 10 and 30 mg.kg(-1). Our data showed that propranolol did not modify the evolution of of oestrous cycles even if plasma prolactin levels have been increased by the highest dose used (30 mg.kg(-1).

Animals↗

[Use of intramuscular lidocaine in the acute stage of myocardial infarction].

Methods of using intramuscular lignocaine and its relay with an intravenous infusion were studied in 34 patients with reference to serum levels. A first group of 9 patients with myocardial infarction received an intramuscular injection of 300 mg lignocaine into the deltoid or gluteral muscles at five day intervals. The deltoid appears to be the better site of injection in patients confined to bed because of its quick absorption, higher serum levels between the 15th and 90th minute (+47%), and longer duration of action (180 compared to 120 minutes). The difference is not observed in ambulatory patients and seems to be related to sluggish circulation in the gluteral muscles during bed rest. Its relay with intravenous infusion was studied in 14 patients. In the first 6 patients, intradeltoid injection was immediately followed by an infusion of 2.5 mg/mn, giving an average plasma lignocaine level between the 15th and 60th minute greater than 5 mu/ml. In the 8 other patients, a period of I hour was allowed to elapse before starting the infusion. The plasma levels were found to be within the therapeutic range in all patients and no side effects were observed. The administration of an intravenous infusion of 150 mg/hr of lignocaine for 48 hours led to excessively high plasma levels in 8 patients at the 24th hour, 3 of whom had side effects. Reducing the dosage to 100 mg/hr from the 12th hour onwards in II patients avoided this complication. A 300 mg intradeltoid injection of lignocaine is easy to give in the patient's home and therefore, is the best adapted method for the pre hospital treatment of myocardial infarction. When necessary, it may be relayed with an intravenous infusion one hour later, in the coronary care unit.

Aged↗

[An experimental study of veralipride (author's transl)].

The administration of doses of 0,001, 0, 01, 0,1, and 1 mg/kg/day of veralipride to female rats produces a dose-related blocking effect on dioestrus. No histological changes are noted in the genital tract and mammary gland tissues after 0,001 and 0,01 mg/kg/day. Doses of 0,1 and 1 mg/kg/day block ovulation and the resulting estrogen impregnation modifies the appearance of the uterine glands and vaginal epithelium. Mammotropic effects, seen as a moderate hyperplasia but without galactogenic secretion, occur after 1 mg/kg/day only.

Animals↗

[Effects of cimetidine on estrus cycle in the rat].

Statistical study of Cimetidine effects on estrous cycle of the rat have been performed, by daily vaginal smears, for twenty one days with doses nearly similar to those used in human therapy. Our data showed that Cimetidine did not significantly modify the evolution of estrous cycles.

Animals↗

[Comparative statistical study of two antiemetics, metoclopramide and metopimazine, effects on the oestrus cycle in the female rat (author's transl)].

A comparative study of two antiemetic neuroleptics, metoclopramide and metopimazine, effects on the oestrus cycle of female rats has been done. These compounds were administered once daily for 21 consecutive days (1, 0,1, 0,01, 0,001 mg/kg/s.c.) on Wistar AFSPF rats, exhibiting regular four day cycles. Evolution of oestrus cycle was studied by daily vaginal smears. Our data show that metoclopramide does not influence oestrus cycle, while metopimazine suppress oestrus cycles, substituted for a permanent dioestrus. For the last compound, a statistically significant difference between treated and controls is demonstrated.

Animals↗

[Undesirable effects of antibiotics].

A restatement of the principal mechanisms involved in the production of unwanted side-effects to antibiotics: immediate or delayed hypersensitivity immunological reactions; tissue toxicity (renal and liver parenchyma), damage to the bone marrow and the neurosensory system; interference with metabolism and drug interactions; the development of resistant strains and the risk of secondary infection. Principal unwanted effects associated with the preparation employed, with the organ involved and with the overall physiopathological state. Certain specific side-effects occur with some antibiotic combinations and following drug interactions.

Adult↗