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1.
Toxicol Sci ; 61(2): 273-82, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11353136

ABSTRACT

The aim of this study was to determine whether respiratory acidosis favors the cerebral distribution of cyanide, and conversely, if respiratory alkalosis limits its distribution. The pharmacokinetics of a nontoxic dose of cyanide were first studied in a group of 7 rats in order to determine the distribution phase. The pharmacokinetics were found to best fit a 3-compartment model with very rapid distribution (whole blood T(1/2)alpha = 21.6 +/- 3.3 s). Then the effects of the modulation of arterial pH on the distribution of a nontoxic dose of intravenously administered cyanide into the brains of rats were studied by means of the determination of the permeability-area product (PA). The modulation of arterial blood pH was performed by variation of arterial carbon dioxide tension (PaCO2) in 3 groups of 8 anesthetized mechanically ventilated rats. The mean arterial pH measured 20 min after the start of mechanical ventilation in the acidotic, physiologic, and alkalotic groups were 7.07 +/- 0.03, 7.41 +/- 0.01, and 7.58 +/- 0.01, respectively. The mean PAs in the acidotic, physiologic, and alkalotic groups, determined 30 s after the intravenous administration of cyanide, were 0.015 +/- 0.002, 0.011 +/- 0.001, and 0.008 +/- 0.001 s(-1), respectively (one-way ANOVA; p < 0.0087). At alkalotic pH the mean permeability-area product was 43% of that measured at acidotic pH. This effect of pH on the rapidity of cyanide distribution does not appear to be limited to specific areas of the brain. We conclude that modulation of arterial pH by altering PaCO2 may induce significant effects on the brain uptake of cyanide.


Subject(s)
Acidosis, Respiratory/metabolism , Alkalosis, Respiratory/metabolism , Brain/metabolism , Cyanides/pharmacokinetics , Animals , Blood Pressure/drug effects , Brain/drug effects , Carbon Dioxide/pharmacology , Cyanides/administration & dosage , Cyanides/blood , Hydrogen-Ion Concentration , Hyperventilation/chemically induced , Hypoventilation/chemically induced , Oxygen/pharmacology , Rats , Rats, Sprague-Dawley , Sucrose/blood , Time Factors
2.
Article in French | MEDLINE | ID: mdl-2488662

ABSTRACT

The authors set up an evaluation of the Prevention Program against Blindness in the Center and South areas of Tunisia. They point out an important improvement of the endemo-epidemiological situation, but, nevertheless, they stress the necessity of carrying on the measures of the campaign.


Subject(s)
Blindness/prevention & control , Trachoma/epidemiology , Adult , Blindness/etiology , Child , Child, Preschool , Humans , Trachoma/complications , Tunisia
3.
Eye (Lond) ; 3 ( Pt 2): 204-9, 1989.
Article in English | MEDLINE | ID: mdl-2620749

ABSTRACT

Ocular infection with Chlamydia trachomatis, whether of genital or endemic trachoma origin, usually produces diffuse infiltration and swelling of the scleral limbus, grey infiltrates of the corneal limbus, and superficial extension of vessels onto the corneal limbus. In genitally transmitted C. trachomatis infections, subepithelial infiltrates have been reported as well. In classic endemic trachoma, limbal changes also include limbal follicles which resolve, leaving Herbert's peripheral pits, and an extensive vascular pannus. To evaluate the limbal changes in trachoma, follow-up studies were done in 1986-1987 in a group of 213 children originally seen between 1969-1972. Pannus formation occurred at a much earlier age than conjunctival scar formation and was an excellent predictor of later severe conjunctival scarring. The evidence from this study suggests that the mechanisms for corneal pannus formation from the limbus are quite different from those for scarring of the conjunctiva.


Subject(s)
Chlamydia Infections/epidemiology , Cornea/pathology , Eye Infections, Bacterial/epidemiology , Sclera/pathology , Trachoma/epidemiology , Adolescent , Adult , Chlamydia Infections/pathology , Conjunctiva/pathology , Cornea/blood supply , Cornea/immunology , Eye Infections, Bacterial/pathology , Follow-Up Studies , Humans , Longitudinal Studies , Risk Factors , Sclera/immunology , Trachoma/pathology , Tunisia
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