[Oxygen biochemistry. I. Reactive species of reduced oxygen and endogenous sources].
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Biomedical subjects
Publications and source records attributed to M Filip.
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The effect of six 5-HT3 receptor antagonists: ondansetron (0.01-3 mg/kg ip), granisetron (0.01-1 mg/kg ip), zacopride (0.01-3 mg/kg ip), tropisetron (0.001-0.1 mg/kg ip), MDL 72222 (0.01-3 mg/kg ip) and DAU 6215 (0.01-3 mg/kg sc) were examined in the conflict drinking test (Vogel test) and in the elevated plus-maze test in rats. Ondansetron (0.1-0.3 or 1 mg/kg), zacopride (0.1-1 mg/kg) and tropisetron (0.01 mg/kg) increased the punished responding in the Vogel test and showed anxiolytic effects in the elevated plus-maze test. Their effects were limited to a narrow dose range and were not dose-dependent. Granisetron (0.1 mg/kg) exhibited an anti-conflict activity, but was ineffective in the elevated plus-maze test. MDL 72222 and DAU 6215 were ineffective in both those tests. On the other hand, diazepam (2.5-10 mg/kg), used as a reference drug, was active in either procedure and its effects were dose-dependent. These results indicate that an anxiolytic-like activity is not a common characteristic of 5-HT3 receptor antagonists. Moreover, even the anxiolytic action of drugs which were active in the experimental models used should be accepted with caution.
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Authors report the case of a patient in whom a sympathetic ophthalmia with posterior onset under the aspect of a massive CRSC was diagnosed. The clinical and therapeutic aspects are described in detail.
The coenzymatic capacity of NAD+ decreases by exposing it to the action of ascorbic acid--Cu(II) system, a generator of free radicals. The participation of the radicals in degrading NAD+ depends on the nature of the buffer, incubation medium pH, temperature, incubation time. Thiourea, IK, GSH, cysteine, mannitol, albumine reduce to different extents the noxious action of the radicals. The decrease of the coenzymatic function of NAD+ is caused by the break of esther and anhydride links, evidenced by releasing th cian-sensitive compounds--nicotinamide riboside and nicotinamide ribonucleotide. Also the presence of ortophosphate was demonstrated.
Detachment of the retina is still a very serious ocular disease which poses many problems to the ophthalmologist. The study shows the causes of the treatment failure in this disease on the basis of the authors' experience and the specially literature.
The authors review the principal elements linked to the use of cortisone in ophthalmology, emphasizing new facts concerning the action of cortisone and especially the problems connected with this treatment.
Pseudophakia generates a new pathology, sometimes atypically solved, insufficiently codified yet. The paper presents the experience on quite a large group of cataract-operated patients with implantation of pseudofac, in which cases of ocular hypertonia appeared.
The paper reports on the author's own experience in the surgical treatment of the traumatic cataract in children. The authors consider that implantation of the artificial crystalline must not be a general implantation method, in any eye. It has to be made discriminatingly and take into consideration the posttraumatic inflammatory reactions and the local state of each eye.
The action of N-2 (p-chlorophenoxy isobutiril)-N-morpholino-methylureea on some serum lipids parameters in rats with normolipemia and tritonic hyperlipidemia was studied. In the animals with normolipidemia, the compound induces hypocholesterolemia beginning with the 5th day of treatment, hypotriglyceridemia during the entire investigation interval and an increase of phospholipid levels in the 9th day of treatment. In the rats with tritonic hyperlipidemia, the substance induces hypocholesterolemia, hypotriglyceridemia, increase of HDL-cholesterol levels, decrease of (VLDL + LDL)--cholesterol levels and the return to normal values of Glueck ratio.
In view of improving the cutaneous bioavailability of alpha-chymotrypsin from ointments, the stability of this enzyme in two hydrophile ointment bases, macrogoli and carbopol, was tested. The cutaneous bioavailability of alpha-chymotrypsin in ointments, estimated by determining the anti-inflammatory action, underlines the important role played both by the ointment base and by the enzyme activating substances. By correlating the determinations of alpha-chymotrypsin enzymatic activity with the anti-inflammatory action a correlation between the manifested activity and the active substance stability was noticed.
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Explore the source record for details and available documents.
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