PubMed Health⌕ Search

Biomedical subjects

W H Ford

Publications and source records attributed to W H Ford.

14 recordsLinked to original sources

A developmental toxicity study of tretinoin administered topically and orally to pregnant Wistar rats.

BACKGROUND: Although it is well established that oral tretinoin produces embryofetal developmental toxicity in various laboratory animals, the toxic potential of topical tretinoin has not been clearly established. OBJECTIVE: This study of tretinoin administration to pregnant Wistar rats was conducted to determine whether topical tretinoin is associated with adverse effects on reproductive function or embryofetal growth and development and to compare outcomes with topical and oral tretinoin. METHODS: Topical and oral tretinoin (1 to 20 mg/kg and 1 to 10 mg/kg, respectively) or vehicles alone were administered on gestational days 6 through 16 and 15, respectively. RESULTS: Topical tretinoin: After topical treatment, dams receiving 10 mg/kg daily or greater had severe local and systemic toxicity prompting discontinuation of tretinoin. At doses of 2.5 mg/kg or greater, dam weight gain and food consumption were significantly less than those of control dams. Offspring of dams receiving 5 mg/kg weighed significantly less, and offspring of dams receiving 2.5 mg/kg or greater had a significantly greater occurrence of supernumerary ribs compared with control offspring. Oral tretinoin: After oral treatment, in the absence of maternal toxicity, significantly more offspring of dams receiving 5 mg/kg or greater had supernumerary ribs, and offspring of the 10 mg/kg treatment group had a greater incidence of cleft palate than had control offspring. CONCLUSION: The local and systemic maternal toxicity found in association with supernumerary ribs and low weights in the offspring at topical tretinoin doses of 2.5 and 5 mg/kg suggests that these developmental effects may be nonspecific or maternally mediated. Oral tretinoin at doses of 10 mg/kg, however, is clearly associated with embryofetal alterations in the Wistar rat.

Abnormalities, Drug-Induced↗

Induction of maternal toxicity in the rat by dermal application of retinoic acid and its effect on fetal outcome.

Time-mated Sprague-Dawley rats were administered all-trans-retinoic acid (RA) dermally on gestational days 11 through 14 at three dosage levels (25, 100, and 250 mg/kg body weight). Dams administered ethylenethiourea (ETU) dermally on gestational days 11 to 12 or RA orally on day 12 were used to indicate the strain's sensitivity to teratogenesis. The chemicals were dissolved in dimethylsulfoxide (DMSO) for dermal application or suspended in corn oil for treatment by gavage. The maternal weight gain, pup weight, number of resorptions and number of fetuses with gross malformations, and skeletal/organ-level anomalies were determined. Beginning with day 15, dams dermally treated with RA exhibited dermal lesions at the site of application, most dams showed vaginal bleeding by day 16, and approximately 20% did not survive to day 19. Relative to the DMSO control group, maternal weight gain in the dermal RA groups was decreased by approximately 50% at the lowest dose, with essentially no weight gain at the intermediate- and high-dose levels. The decrease in average fetal weight at the two higher doses was significant, whereas the resorption and malformation frequencies were not significantly increased by dermal treatment with RA. Without significantly affecting fetal weight or resorption frequency, dermal application of ETU significantly increased the frequency of skeletal anomalies, primarily tail defects. Oral administration of RA did not increase the malformation frequency nor produce significant maternal or fetotoxic effects. In summary, treatment of pregnant Sprague-Dawley rats by dermal application of RA dissolved in DMSO resulted in significant toxicity to the dam.(ABSTRACT TRUNCATED AT 250 WORDS)

Abnormalities, Drug-Induced↗

Effects of variation in the level of haptenation of heterologous protein immunogen on cellular and humoral responses of the guinea pig.

Groups of guinea pigs were sensitized with bovine gamma-globulin (BGG) substituted with 0, 4, 12, or 40 dinitrophenyl (DNP) groups per molecule. Skin tests, lymphocyte stimulation, two lymphokine assays and antibody determinations were carried out after 21 days using all four antigens. In the extreme situations when BGG-sensitized animals were challenged with DNP40-BGG, or when DNP40-BGG-sensitized animals were challenged with BGG, the delayed skin reactions were transient and weakly indurated. BGG-sensitized guinea pigs injected with anti-DNP40-GBB serum showed no change in delayed skin response to DNP40-BGG, whereas anti-BGG serum enhanced the response of DNP40-BGG-sensitized anamals to BGG. All immunized groups showed lymphocyte stimulation and lymphokine production by all antigens, but migration inhibition and lymphocyte stimulation followed less closely the pattern of delayed skin responses than did mitogenic factor output. The serum antibody response to DNP40-BGG as immunogen indicated that all carrier determinants were masked. At lower levels of substitution, anti-hapten titres were reduced and appreciable levels of anti-carrier antibody obtained.

Animals↗

Effect of the concentration of inducing agent on the output of lymphokines in the guinea pig.

The production of migration inhibition (MIF) and mitogenic (MF) factors by cultured guinea pig lymph node cells was examined as a function of the concentration of antigen or concanavalin A (ConA). Maximum output of MIF was achieved at comparatively low levels of antigen and was equal to the maximum output by ConA. In contrast, MF output increased up to the highest antigen concentrations tested. Kinetic and chromatographic analysis revealed no differences between the MF produced at high and low antigen concentration.

Animals↗

Mitogenic factor as an in vitro correlate of delayed hypersensitivity in the guinea pig.

The relationship of mitogenic factor (MF) to delayed hypersensitivity was examined in the guinea pig. MF was readily produced in vitro by blood leucocytes from animals sensitized with Keyhole limpet haemocyanin in Freund's complete adjuvant. Such animals exhibited delayed skin reactions and macrophage migration inhibition. Treatment with cyclophosphamide markedly reduced serum antibody but caused no diminution of MF or delayed skin reactions. A migration inhibition response was observed 10, but not 20, days after sensitization by means of incomplete adjuvant.

Animals↗

A microplate culture method for assay of guinea pig mitogenic factor.

An improved method for assay of guinea pig mitogenic factor (MF) is described. The technique is based on the use of thymocytes in microplate cultures and yields significant savings in time, labour and materials. The quantitative potential of the assay is examined using antigen- and concanavalin A-indiced MF, and its application to assessing in vitro immune responsiveness of individual guinea pigs is explored.

Animals↗

Comparsion of the properties of two antigen-induced guinea pig lymphokines.

The properties of macrophage migration inhibition factor (MIF) and mitogenic factor (MF) were compared using culture supernatants of antigen-stimulated lymph node cells from inbred guinea pigs. Gel filtration on Sephadex G-100 indicated molecular weights of about 60,000 and 25,000 for MIF and MF, respectively. The lymphokines also differed with respect to heat sensitivity, MIF being largely inactivated by 60 degrees C for 20 min, whereas MF was unaffected by this treatment. The time course of production, antigen specificity of induction, and susceptibility to neuraminidase were also examined.

Animals↗