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Biomedical subjects

J Weinberg

Publications and source records attributed to J Weinberg.

At least 145 records · Page 8Linked to original sources
PubMed1990

A simple transnasal procedure for treating choanal atresia.

Bilateral choanal atresia is a rare but life-threatening disorder. Prompt diagnosis and emergency treatment are necessary. Various transnasal tools as well as other techniques have been tried in the past: they have all been associated with complications. The authors report a treatment of a newborn with a simple and previously unreported procedure for dealing with bilateral choanal atresia. As described, the use of a simple hand-powered drill and bit offers an approach which is straightforward and free of complications. Efficacy of this procedure is documented by a 6-year follow-up period.

Choanal Atresia↗
PubMed1990

Biochemical evaluation of calcium stone patients: how soon can it be done after stone surgery/passage?

Biochemical evaluations were done two times for 29 outpatients with calcium stone disease, the first time within one month after surgical extraction or passage of stones and the second time two months or more later. Classification of the etiologic basis for the stone disease was the same after both tests in 27 patients. In the other 2 patients the diagnosis was changed from renal to absorptive hypercalciuria. Both of these patients had creatinine clearance rates less than 60 percent of normal during the first test. One also had multiple residual stones during both evaluations, and the second had a urinary tract infection during the first test that resolved with a normal creatinine clearance by the second test period. When nephrogenous cyclic adenosine monophosphate (cAMPn) assays were done on fasting specimens in these patients, the results were consistent with absorptive hypercalciuria. Almost all patients can be evaluated and placed in management programs within a few weeks after surgery. If cAMPn assays are not done, patients with decreased renal function secondary to residual stones or infection can be tested at a later time.

Adolescent↗
PubMed1990

A histological study of the Shionogi adenocarcinoma 115 grown in male and female mice.

We have previously demonstrated that growth rate and morphology differ between androgen-responsive Shionogi mouse mammary tumours maintained in male and female mice. Furthermore, we can modulate the growth rate of these tumours in male mice by exposing the mice to psychosocial stressors. In the present study, we were interested in determining if tumours in male mice with a comparable growth rate to that in females, also had a morphology similar to that in females. SC115 tumours were examined using histochemical and immunohistochemical techniques. Tumours in male mice were easily distinguishable from tumours in female mice regardless of growth rate. Tumours maintained in female mice contained osteoid-like regions which stained positive for sialic acid and sulphate moieties. No such regions were observed in any of the tumours from male mice. In addition, although all tumours contained MSA (muscle specific actin)-positive and S100 protein-positive cells, these regions were more extensive in the tumours of female mice. This study suggests that tumour growth rate and morphology are independently regulated by the host environment.

Actins↗
PubMed1989

Effects of psychosocial stressors on mouse mammary tumor growth.

We describe a sensitive and replicable animal model which demonstrates that psychosocial variables both increase and decrease tumor growth rate. The effects of social housing condition and daily exposure to novel environments were investigated in mice bearing the transplantable androgen-responsive Shionogi mouse mammary carcinoma (SC115). Being reared individually housed and remaining individually housed or being reared in a sibling group and then singly housed following tumor cell injection markedly increased tumor growth compared to that in mice remaining in their standard sibling rearing groups (n = 2-3 per group), if animals were also exposed to acute daily novelty stress. In contrast, being reared individually and then moved to a larger social group (n = 4-5 nonsiblings per group) markedly reduced tumor growth, both in the presence and absence of acute daily novelty stress.

Animals↗
PubMed1989

Prenatal ethanol exposure alters adrenocortical development of offspring.

Interactive effects of prenatal ethanol and maternal nutritional status on reproductive outcome and maternal and offspring adrenocortical activity were examined. Ethanol was administered to pregnant females in liquid diets (36% ethanol-derived calories) which were marginal or optimal in terms of requirements for pregnancy. Both pair-fed and ad libitum fed control groups were included. Females consuming ethanol from gestation Day 1 through parturition gained less weight, were delayed in parturition, and had fewer and smaller live born young than pair-fed or control females, regardless of whether they consumed marginal or optimal diets. Withdrawing ethanol on Day 21 of gestation attenuated many of ethanol's adverse effects on reproductive outcome. However, prenatal maternal ethanol intake altered adrenocortical activity/responsiveness of the mother, the fetus, and the preweaning offspring, regardless of maternal nutritional status. Relative adrenal weights and basal corticosterone levels were increased in the dam both prenatally and at parturition. Ethanol-exposed fetuses (A) had increased relative adrenal weights but lower basal corticosterone levels than pair-fed (PF) and control (C) fetuses on gestation Day 21. At birth, plasma and adrenal corticosterone levels were increased, while absolute adrenal weights and corticosterone binding globulin (CBG) binding capacity were decreased in A neonates. At 5 days of age, A pups showed reduced plasma corticoid responses to ether at 15 min poststress and to novelty or saline injection at 90-min post stress compared to PF and C pups. CBG binding capacity was also reduced in A pups. At 10 days of age, plasma corticosterone levels were lower overall in A and PF than in C pups following exposure to a number of different acute stressors while at 18 days plasma corticoids were decreased and adrenal corticosterone was increased in A compared to PF and/or C pups. These data support and extend previous studies indicating that in utero ethanol exposure alters postnatal adrenocortical development. This effect is specific to ethanol and unaltered by maternal nutritional status.

Adrenal Cortex↗
PubMed1989

Spurious hyperphosphatemia in patients with dysglobulinemia.

Following the introduction of the ASTRA automated chemical analyzer to the Brooklyn VA Hospital, we identified 14 patients with normal renal function and marked hyperphosphatemia (9.1 +/- 3.1 mg/dl). Reanalysis of these samples by standard SMA-II autoanalyzer demonstrated normal phosphate concentration (3.5 +/- 0.7 mg/dl). All patients had a dysglobulinemic syndrome and further examination indicated that ASTRA reagents produced significant optical turbidity in these sera. We conclude that chemical analysis of inorganic phosphorus by methods which do not deproteinate sera prior to colorimetric analysis are subject to nephelometry in the presence of dysglobulinemic samples and may result in spurious hyperphosphatemia.

Aged↗
PubMed1988

Hyperresponsiveness to stress: differential effects of prenatal ethanol on males and females.

In this study we investigated the hypothesis that pituitary-adrenal response inhibition is compromised in animals prenatally exposed to ethanol. In the first experiment, we examined whether opportunity to perform a consummatory response reduces the adrenocortical response to a novel test cage. Animals were water deprived for 24 hr and tested in one of three conditions: (a) removed from home cage, blood sample obtained immediately; (b) placed into empty novel cage, blood sample obtained 30 min later; (c) placed into novel cage with water available, blood sample obtained 30 min later. All animals showed an increase in corticoids over basal levels following 24-hr water deprivation, and placement into a novel cage produced a further significant increase in corticosterone. Opportunity to drink reduced the corticosterone response to novelty for all males. However, fetal ethanol-exposed females showed significantly less attenuation of their corticosterone response to novelty than both pair-fed and control females. In the second experiment, we examined adrenocortical habituation to a stressful stimulus. Animals were restrained in plastic tubes which restricted movement, and blood samples were obtained following 30 or 60 min of restraint. All animals showed significant corticoid elevations at 30 min. Males showed no change in corticoids from 30 to 60 min while both pair-fed and control females showed a corticoid decrease at 60 min. Fetal ethanol-exposed females, however, showed no significant corticoid decrease at 60 min.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1988

Time-resolved pulsed fluorescence immunometric assays of carcinoembryonic antigen.

A time-resolved pulsed fluorescence immunometric assay (TR-PFIA) for carcinoembryonic antigen is described in which either Eu(III) or Tb(III) chelate is used as label. Described in detail is the assay involving the well-documented format of microtiter matrix and Eu(III) fluorescence enhanced with a beta-diketone and quantified in a commercial time-resolving fluorometer. We have also used the same basic assay, but one with a Tb(III) chelate as label, and we read the fluorescence signal directly off a surface without the application of enhancement solution. The Tb(III) fluorescence is then brought into solution by using an analog of dipicolinic acid in an enhancement solution. The latter approach demonstrates the scope of the methodology, which invokes the extra complexity of enhancement only when increased sensitivity might be required. The power and versatility of the enhancement methodology are demonstrated.

Carcinoembryonic Antigen↗
PubMed1987

Effects of early experience on responsiveness to ethanol: a preliminary report.

The present study examined the hypothesis that early experiences which alter an organism's response to novel or aversive stimuli and hence its ability to cope with stress might also alter sensitivity to and preference for alcohol. On day 1 of pregnancy, females were assigned to 1 of 5 groups: Handled (H), Nonhandled (NH), Malnourished (MAL), Prenatally stressed (PRE) or Control (CON). Offspring were tested in adulthood to measure their adrenocortical response to stress (ether plus cardiac puncture), adrenocortical response to IP ethanol injection and alcohol preference. Data indicate that early experience did alter responsiveness to stress in adulthood; early handling decreased later stress responsiveness and prenatal stress increased later stress responsiveness. In addition, although early experiences did not alter the corticosterone response to IP ethanol at 60 min post injection, both preweaning handling and perinatal malnutrition reduced alcohol preference in adulthood.

Adrenal Cortex Hormones↗
PubMed1987

Alcohol-induced changes in pituitary-adrenal activity during pregnancy.

This study examined the interactive effects of ethanol and nutritional status on pituitary-adrenal function of pregnant females consuming high doses of ethanol throughout gestation. Three liquid diets were formulated ranging in protein content from suboptimal to supraoptimal (18%, 25%, or 32% of total calories) in terms of pregnancy requirements, while ethanol was held constant at high levels (36% of total calories). In addition to the alcohol group (A), both pair-fed (PF) and ad libitum-fed control (C) groups were included in each diet regimen. Basal levels of corticosterone and the adrenocortical response to stress were measured in dams on days 11, 16, or 21 of gestation. Plasma levels of corticosterone-binding globulin (CBG) were also measured on gestation days 16 and 21. Maternal adrenal weights, basal corticosterone levels, the adrenocortical response to stress, and the corticoid stress increment were all significantly increased in A compared to both PF and C females. Plasma CBG levels of A females were similar to or less than those of PF and C females. Thus alcohol consumption significantly increased maternal pituitary-adrenal activity as early as day 11 of gestation and these effects on hormonal function increased as gestation progressed. This adrenocortical hyperactivity was relatively unaffected by maternal nutritional status and thus appears specific to alcohol.

Alcoholism↗
PubMed1986

Adrenocortical responsiveness to novelty in the hamster.

The adrenocortical response to increasing periods of exposure to a novel cage, as well as the effects of returning hamsters to their familiar home cages, were examined. We found that a five min exposure to a novel cage was insufficient to activate the pituitary-adrenal system, but that cortisol levels increased significantly as duration of exposure increased from 15 to 30 min. In contrast, returning hamsters to their home cages for at least 15 min following the 15 min novel cage exposure produced a significant drop in plasma levels of cortisol. Finally we found that males exhibit a greater cortisol response to novelty than females, indicating a sexual dimorphism which is the reverse of that reported in other rodents.

Adrenal Cortex↗
PubMed1986

Motility of isolated mammalian gastric fundus.

Gastric fundus strips (GFS) of rats, guinea-pigs, rabbits, cats and humans, but not of dogs, show spontaneous phasic contractions in vitro. Rabbit, cat, dog and human GFS exhibit dose-dependent responses to acetylcholine (ACh), histamine (His), serotonin (5-HT) and KCl. Guinea-pig drug-induced responses are not dose-dependent. Rat GFS does not respond to His. ED50S for KCl are always higher than for other agonists. ED50S for 5-HT are lower than for other drugs in rats and cats, but not different in other species. Maximal GFS contractions induced by ACh are usually higher than those induced by other drugs.

Acetylcholine↗