Étude cinétique de l'hypersensibilité de type retardé dans la candidose expérimentale de la souris

Mice were inoculated with different quantities of blastospores ofCandida albicans by subcutaneous or intravenous ways. Delayed hypersensitivity was then studied during the course of infection by means of the inhibition of macrophage spreading test. In the same time retrocultures were done from kidney material, target organs in the experimental candidiasis. The results obtained in this way enabled the authors to think that cellular immunity plays a role in this experimental model as described by Mackaness.

Travail de l'Unité 42 de l'INSERM et du Groupe de Mycologie Fondamentale et Appliquée de LILLE.     

Activité cytokinine de dérivés acylés,alkylés,acyl-alkylés de l'adénine et d'isost`eres azotés de la γ,γ-diméthylallyladénine

The cytokinin activities of various 6-acylaminopurines, 6-alkylaminopurines, 6-acylamino-9-benzyl-purines as well as a series of isosteric-nitrogen derivatives of N⁶-(γ, γ-dimethylallyl)adenine (I⁶Ade) have been tested using the tobacco pith and the pea bud bioassays. The interactions between active, slightly active and inactive compounds have been studied with the last assay. Acylation decreases the biological activity; e.g., N⁶-benzoyl and N⁶-furoyladenines are less active than Na⁶-benzyladenine and kinetin. Substitution at the 9-position reduces (tobacco-pith assay) or suppresses (pea-bud assay) the phytohormonal activity of otherwise active 6-acylaminopurines. In isosteric derivatives, maximum activity occurs when the side chain has the same length as in 1⁶Ade. After the analysis of interactions between more or less active compounds, it is suggested that the differences in cytokinin activity could be related to unequal affinities for a hypothetical receptor site.     

Conséquences de la chimiothérapie anticancéreuse sur la fertilité de la femme

Sterility is a potential toxic effect of chemotherapy. This risk is well established for alkylating agents, but is less clearly defined for anthracyclines, methotrexate and fluorouracil and poorly defined for alkaloids, platinum, etoposide and taxanes. The main predictive factors for ovarian toxicity are the additive effect of cytotoxic drugs, the cumulative dose of each drug and the patient’s age. This effect of chemotherapy is evaluated on menstrual cycles, hormonal assays and the number of pregnancies observed in patient cohorts. Chemotherapy induces destruction of oocytes and granulosa cells. In mice, it has been shown that adriamycin may induce oocyte apoptosis, which can be prevented by modulation of cycle cell signalling (dysregulation of Bax gene or, on the contrary, expression of its antagonist gene Bcl-2 or inhibition of apoptosis with sphingosine-1-phosphate or caspase inhibitors). Clinical data in the literature are usually based on retrospective studies and are somewhat confused: global fertility after MOPP chemotherapy for Hodgkin’s disease is about 20%, adjuvant chemotherapy with CMF, F(A)C or TAC for breast cancer induces amenorrhea in 50% to 70% of cases, PVB or BEP chemotherapy for ovarian germ cell tumors has little effect on fertility when the uterus and one ovary can be preserved, and the majority of women treated with methotrexate, actinomycin D or various combinations for persistent trophoblastic disease remain fertile. Preservation of fertility is a major goal for cancer patients receiving chemotherapy: in vitro fertilization could preserve the couple’s fertility, but is usually not feasible as it would delay initiation of chemotherapy until after stimulation of ovulation; oocyte or ovarian tissue cryopreservation is at the stage of research; oral contraceptives have not been demonstrated to be effective to preserve ovarian function; gonadotropin releasing hormone (GnRH) agonists prevent cyclophosphamide toxicity in rat and monkey ovaries, and a few pilot clinical studies suggest that chemotherapy-induced amenorrhea could be prevented by administration of GnRH analogues simultaneously to chemotherapy, but randomised studies are necessary.     

Influence de la température sur la cinétique,de croissance et le coefficient de maintenance de Candida lipolytica cultivé sur n-alcane

The effect of growth temperature on the evolution of kinetic parameters and yields was determined for Candida lipolytica cultures with ntetradecane as substrate, in a temperature range of 18°C to 30°C, which is below the critical growth temperature in order to work only in the activation zone of these parameters.In such a culture limited by substrate transfer, growth rate depends on biological rates, related to microorganisms characteristics, and diffusional rates, related to mass transfer. The effect of temperature thus depends on the limiting step. The activation energy, calculated from exponential growth rate determinations is .When the activation energy is calculated from the maximal rate of cell production (determined at the growth curve's inflexion point), it's found to be E _X=71,200 J/mole in the 18°C–24°C range, and E _X=28,000 J/mole in the 24°C–30°C range. The latter one is characteristic of a diffusion-limited process. Above 24°C, growth is controlled by substrate-transfer, as physiological potentialities are preferentially increased with temperature than diffusional ones: 24°C is thus the transition temperature T _t from physiological to diffusional limitation.The apparent yield is almost constant, over the 18°C to 30°C temperature range, although maintenance coefficients are very dependent on temperature. The activation energies related to maintenance coefficients for alkane and oxygen respectively are and .The m _s/m_{O 2} ratio is about 3 (g/g), whereas that, for a strict oxidation reaction of n-tetradecane ought to be 3.47 (g/g). A satisfactory correlation, relating maintenance coefficients to the maximal growth rate of yeast, is given.

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Liste des symboles A constante de saturation de modèle de croissance(1) - B vitesse spécifique considérée - C substrat carboné ou oxygène (g/l) - E energie d'activation (J/mole) - S _m quantité de substrat consommée par maintenance au cours d'une fermentation discontinue (g) - O₂ quantité d'oxygène transférée au milieu de culture (g/l) - R rendement global de la fermentation - R rendement global de la fermentation - constante des gaz parfaits (J/mole K) - S concentration en substrat carboné (g/l) - T température de croissance (°K) - X concentration en biomasse (g/l) - Y rendement limite - m coefficient de maintenance (h^-1) - t duree de fermentation (h) - tømpérature de croissance (^o Celsius) - taux de croissance (h^-1) Indices 1 relatif à la température 1. - 2 relatif à la température 2 - c relatif au substrat carboné ou à l'oxygène - f relatif au temps final - i relatif au point d'inflexion - m maximum - mO₂ relatif au coefficient de maintenance sur l'oxygène - m _s relatif au coefficient de maintenance sur le substrat carboné - o relatif au temps initial - O₂ relatif à l'oxygène - s relatif au substrat carboné - t de transition - T relatif à la température de croissance T - U _m relatif au taux de croissance maximal - X relatif à la productivité maximale en biomasse     

Activité cholinestérasique des corpuscules sensoriels cutanés de Herbst et de Grandry

Résumé L'activité cholinestérasique (ChE) a été étudiée dans les corpuscules de Herbst et de Grandry du bec de canard par la méthode de Karnovsky. Le BW 284 C 51, l'iso-OMPA et l'ésérine ont été utilisés comme inhibiteurs. Une activité cholinestérasique non spécifique (nsChE) a été identifiée dans les corpuscules. Elle est présente dès le début de leur différenciation.Corpuscule de Herbst: l'activité nsChE est localisée dans les cellules du bulbe interne (citernes périnucléaires, reticulum endoplasmique granulaire, vésicules associées à l'apppareil de Golgi) et à la surface de la membrane plaamique des cellules du bulbe interne et de la terminaison nerveuse.Corpuscule de Grandry: l'activité nsChE est localisée dans les cellules satellites (citernes périnucléaires, reticulum endoplasmique granulaire) et à la surface de la membrane plasmique des cellules satellites, des cellules de Grandry et de la terminaison nerveuse.Une forte activité nsChE a été mise en évidence dans certaines zones de contact entre les cellules dites sensorielles (cellules du bulbe interne et de Grandry) et les terminaisons nerveuses. Une réaction positive a été observée au niveau des mitochondries des cellules satellites et de la terminaison nerveuse du corpuscule de Grandry, et dans des vésicules du réticulum endoplasmique lisse des terminaisons nerveuses.Aucune activité ChE n'a été détectée dans les cellules capsulaires, les cellules de l'espace interne, les cellules de Grandry, et dans les vésicules synaptiques.Ces résultats ont été discutés en relation avec ce que l'on sait sur l'activité ChE des autres types de corpuseules sensoriels. La signification fonctionnelle de cette activité ChE et le problème de l'origine des différentes catégorics cellulaires qui constituent les corpuscules de Herbst et de Grandry ont été envisagés.

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Cholinesterase activity in the Herbst and Grandry cutaneous sensory corpusclesHistochemical study at the light and electron microscope

Summary Cholinesterase activity (ChE) was localized in the Herbst and Grandry cutaneous sensory corpuscle of the duck beak with Karnovsky's method. Controls with BW 284 C 51, iso-OMPA and eserine were carried out. A non-specific cholinesterase activity (nsChE) was identified in the corpuscles. This enzyme activity is present from the beginning of their differenciation.Herbst corpuscle: nsChE activity was localized in the inner bulb cells (perinuclear cisterna, granular endoplasmic reticulum, vesicles associated with the Golgi complex) and along the plasma membrane of inner bulb cells and nerve ending.Grandry corpuscle: nsChE activity was localized in the satellite cells (perinuclear cisterna, granular endoplasmic reticulum) and along the plasma membrane of satellite cells, Grandry cells, and nerve ending.A high nsChE activity was evident in certain zones of contact between the so-called sensory cells (inner bulb and Grandry cells) and the nerve endings. A positive reaction was seen in mitochondria of satellite cells and nerve ending for the Grandry corpuscle, and in smooth endoplasmic vesicles of the nerve endings.No ChE activity was detected in capsular cells, inner space cells, Grandry cells and in synaptic vesicles.These results are discussed in relation with what is known about ChE activity of other sensory corpuscles. The functional significance of this ChE activity and the problem of the origin of the different cells of Herbst and Grandry corpuscles have been considered.

     

L'évaluation de l'incapacité dermatologique en santé au travail.

This paper presents a simple method for evaluating the extent of impairment in occupational dermatosis based on the portion (P) of the anatomic area involved (A) and the coefficient of physiologic disturbance (C). A percentage value is assigned to each anatomic area on the basis of its functional importance. The coefficient of physiologic disturbance is the average of four factors (stiffness, dehydration, thickening, and pruritus or pain). The formula (P X A). C gives the final percentage of impairment.     

Joseph-Pierre Pétrequin (1809–1876): chirurgien, anatomiste, historien de la médecine, fondateur de la Faculté médicale lyonnaise et son procédé chirurgical original pour la cure de la gangrène de la verge

Pétrequin was an outstanding anatomist, surgeon, medical historian, and founder of the Lyon School of Medicine. This article describes his scientific contribution with particular emphasis on his original surgical procedure for the treatment of penile gangrene.     

Alcaloïdes de Zanthoxylum decaryi: la decarine,nouvel alcaloide dérivé de la benzophénanthridine

Four alkaloids have been isolated from the stem bark of Zatithoxylum decaryi. Three are known, dictamnine skimmianine, 4-methoxy-1- methyl-2-quinolone. The fourth decarine is new; its structure has been established as 9-methoxy-10-hydroxy-2,3-methylenedioxybenzophenanthridine.¹     

Variations de l'incidence des fractures de l'extrémité supérieure du fémur chez les personnes agées de la région de Québec.

To estimate the incidence of fracture of the proximal end of the femur in people aged 50 years or older living in the Quebec area in 1971, 1976 and 1981 we determined the number of admissions for such fractures to the 15 acute care hospitals in the region. From 1971 to 1981 the number of fractures increased by 71%; the increases for those aged 75 to 84 years and 85 years or over were 98% and 118% respectively. The variation is only partly explained by changes in sex and age distribution of the population; the incidence rates also increased. Among men aged 75 to 84 years the incidence rate per 1000 person-years rose from 2.63 in 1971 to 5.22 in 1981, an increase of 98%; the corresponding figures for men aged 85 years or more were 9.76 and 16.91, an increase of 73%. Among women aged 75 to 84 years the rate rose from 7.28 to 8.81, an increase of 21%; the corresponding figures for women aged 85 years or more were 20.40 and 24.27, an increase of 21% and 19% respectively.     

Étude de la variabilité de la clairance hépatique de la mébrofénine-99mTc en scintigraphie hépatobiliaire

AimThe purpose of this study was to investigate some of the parameters likely to influence mebrofenin-^99mTc hepatic clearance calculation and inter-and intra-observers reproducibility.Materials and methodsHepatic clearance (%/min m²) of 30 scintigraphies was calculated from the values of hepatic, cardiac, and total activities, according to the method recommended in the literature. We studied: 1) impact of injection–acquisition delay variations; 2) acquisition type: anterior face only (FA) or geometric mean (GM); 3) clearances calculated according to four different body surface area (BSA) formulas; 4) intra-and inter-observers reproducibility for three observers (two evaluations for each observer).Results1) Clearance differences between different studied intervals were statistically significant, more important if the studied interval was far from reference interval (150–350 secondes) and even more when the interval studied was too early (110–310 secondes). 2) There was a statistically significant difference between clearance calculated using either FA or GM datasets (0.85 %/min m²). 3) There were small but statistically significant differences for four of the clearance comparisons using different BSA formulas. 4) Despite differences in size of cardiac and hepatic regions of interest (ROI), intra-observer reproducibility of hepatic clearance was excellent for each observer. Inter-observers reproducibility was also excellent (r = 0.982).ConclusionHepatic clearance of mebrofenin-^99mTc appears to be a highly reproducible method provided that acquisition and clearance calculation are standardized. It provides additionnal functional information to morphological and biological data usually performed before major hepatectomy. Thereby, the definition of a standardized protocol would enable realization of multicentric studies.