Search PubMed⌕ Search

Biomedical subjects

S Freeman

Publications and source records attributed to S Freeman.

At least 109 records · Page 6Linked to original sources
PubMed1996

Characterization of Colletotrichum gloeosporioides isolates from avocado and almond fruits with molecular and pathogenicity tests.

One hundred twenty isolates of Colletotrichum gloeosporioides from avocado (6 U.S. and 57 Israeli isolates) and almond (57 Israeli isolates) fruits were compared by various molecular methods and a pathogenicity assay in order to determine the genetic diversity and host specificity between and among the different populations. DNA from eight additional U.S. almond anthracnose isolates were also compared. PCR amplification of genomic DNA with four primers produced uniform banding patterns for all the Israeli almond isolates from different geographic locations in Israel. DNAs from the U.S. almond isolates were distinct from DNAs of the Israeli isolates. In contrast, the avocado isolates from Israel and the United States were more diverse, with numerous arbitrarily primed-PCR phenotypes being observed. HaeIII digestion patterns of A+T-rich DNA distinguished between the almond and avocado isolates. Southern hybridization of the repetitive nuclear-DNA element GcpR1 to PstI-digested genomic DNA of almond and avocado isolates revealed no polymorphic fragments among the almond isolates, whereas polymorphic fragments were observed among the avocado isolates. Amplification and subsequent restriction enzyme digestion of the internal transcribed spacer 4 and 5 regions between the small and large nuclear subunits of DNA encoding rRNA failed to distinguish between C. gloeosporioides isolates from a diverse host range. In artificial inoculations, avocado isolates produced various lesions on avocado and almond fruits, whereas the almond isolates infected both fruits at a lower rate.

DNA, Fungal↗
PubMed1996

The role of adrenocortical steroid hormones in the development of hearing.

Based on the findings that adrenocortical hormones are involved in the regulation of Na+, K(+)-ATPase in several tissues and the presence of receptors for these hormones in the ear during auditory development, it has been suggested that these hormones also induce Na+, K(+)-ATPase activity and the endocochlear potential in the ear, leading to auditory function in the fetus-neonate. In order to test this hypothesis, glucocorticoid and mineralocorticoid hormones were injected into rat pups and their auditory development, compared to control litter-mates, was tested by recording auditory nerve-brainstem evoked potentials (ABR). Those who received glucocorticoid hormones had elevated ABR thresholds on post-natal day (PND) 9, others on PND 11 and still others on PND 16, compared to control litter-mates. The ABR thresholds of those injected with mineralocorticoids were not different from those in controls. These results and additional considerations related to the time sequence of the natural appearance of these hormones in the plasma, of their receptors in the ear and the onset of hearing in rat pups makes it extremely unlikely that adrenocortical hormones are involved in the initiation of Na+, K(+)-ATPase pumps and thereby of the endocochlear potential in the inner ear. It is possible that these hormones and their receptors play a role in the later regulation of the number of pumps.

Aldosterone↗
PubMed1996

Thyroxine affects physiological and morphological development of the ear.

The onset and development of distortion product otoacoustic emissions (DPE) representing cochlear amplifier activity were studied in neonatal hyperthyroid (n = 10) and control (n = 10) rat pups. These were compared to the onset and development of auditory nerve-brainstem evoked responses (ABR) representing overall cochlear function, and to morphological development of the ear. DPEs were recorded at an earlier postnatal age to high (8 kHz) frequencies and progressed to lower (3 kHz) frequencies with age. ABRs to high-intensity clicks were recorded at least 2 days before DPEs, although DPE onset at 8 kHz preceded adult-like ABR thresholds. Both ABR and DPEs appeared earlier in the hyperthyroid rats. Histological evidence showed earlier morphological development of the ear in these animals. ABR thresholds and DPE amplitudes matured at a slower rate in the experimental group despite their earlier onset. There was no difference in ABR and DPE thresholds between adult hyperthyroid and control rats. However, in the experimental group, DPEs had smaller amplitudes to high (70 dB SPL) and to low (50 dB SPL) stimulus intensities at low frequencies. Hence, despite thyroxine-injected rat pups having earlier onset of auditory structure and function (lower ABR thresholds and earlier functioning active cochlear amplifier), it appeared that neonatal hyperthyroidism affected the later state of the cochlea, such that DPEs, especially to low-frequency stimuli, were depressed during and after maturation.

Acoustic Stimulation↗
PubMed1996

Transient evoked otoacoustic emissions can be recorded in the rat.

Transient (click) evoked (TEOAE) and distortion product (DPOAE) otoacoustic emissions can be recorded in most normal human ears. Even though DPOAEs have been recorded in many laboratory animals, there has not been much success in recording TEOAEs in non-primate mammals except for guinea pigs. In this study, TEOAEs were unequivocally recorded in every rat (and guinea pig) ear studied by using short pulses (40 microseconds) to generate the clicks and a short (1.1 ms) amplifier gain suppression period. The responses were reproducible in the same rat, above the noise floor and disappeared post-mortem. They were shorter in duration in rats than in guinea pigs and were made up of a broadband frequency spectrum between 2 and 4 kHz. Post-mortem, the TEOAEs to 65 dB SPL clicks disappeared at about the same time as DPOAEs to low stimulus intensities and before the DPOAEs to high stimulus intensities. The ability to record TEOAEs in rats and other animals should permit further experimentation into the basic mechanisms of generation of otoacoustic emissions in general and TEOAEs in particular.

Acoustic Stimulation↗
PubMed1995

Synthesis of 3-arsonopyruvate and its interaction with phosphoenolpyruvate mutase.

3-Arsonopyruvate was prepared in four steps from glycine. The arsenic-carbon bond was formed by a Meyer reaction between alkaline arsenite and 2-bromo-3-hydroxy-2-(hydroxymethyl)propionic acid; the 3-arsono-2-hydroxy-2-(hydroxymethyl) propionic acid formed was oxidized with periodate to give 3-arsonopyruvate. This proves to be an alternative substrate for phosphoenolpyruvate mutase, giving pyruvate, which was assayed using lactate dehydrogenase. The K(m) is 20 microM, similar to that observed for the natural substrate phosphonopyruvate (17 microM), whereas the kcat. of 0.01 s-1 was much lower than that for phosphonopyruvate (58 s-1). Arsonopyruvate competitively inhibited the action of the mutase on phosphonopyruvate.

Arsenicals↗
PubMed1995

Effect of thyroxine on the development of somatosensory and visual evoked potentials in the rat.

The thyroid hormone thyroxine (T4), administered post-natally to neonatal rats, has been shown to accelerate development of auditory function, as expressed by auditory nerve-brainstem evoked responses. This study investigated whether this earlier development was also reflected in other sensory modalities. Rat pups were injected with T4 from the day of birth for 10 consecutive days. Somatosensory evoked potentials, both from the cortex and from sub-cortical structures, and flash-elicited visual evoked potentials (VEP), were recorded at various ages up to 3 months. The recordings were compared with those from control rats from the same litters. Only a minimal difference was found between the experimental and control groups, the most significant being in the VEP at age 12 days, by which time the eyes of most of the experimental rats had opened, which was not the case for the majority of control rats. This difference disappeared with eye-opening in the control rats. Although T4 is known to affect myelinization and synaptic transmission in developing rat brain, this apparently only minimally affects the functioning of the brain as expressed by evoked potentials, both in the short and long term. The main effect of neonatal hyperthyroidism in these rats appeared to be accelerated development of the end organ (the eye and the ear).

Age Factors↗
PubMed1995

Effect of hypoxemia and ethacrynic acid on ABR and distortion product emission thresholds.

Various studies have shown that induction of hypoxemia in animals such that arterial blood oxygen tensions reach 20-30 mm Hg is accompanied by reversible threshold elevations of the auditory nerve-brain-stem evoked response (ABR). In this state, the endocochlear potential (EP) is depressed, causing a smaller potential difference across the hair cells and/or reduced activity of the cochlear amplifier of the outer hair cells. In order to test these possibilities, ABR threshold (an expression of the overall sensitivity of the cochlea) and changes in threshold of the cubic (2f1-f2) distortion product emissions (DPE) (an expression of activity of the cochlear amplifier) were measured in the same cats while the EP was depressed by hypoxemia or by ethacrynic acid. During the episodes of hypoxemia, DPE thresholds were elevated by 10 dB while ABR thresholds were elevated by 22.8 dB. Therefore, it seems that a normal EP is necessary both for normal cochlear transduction (inner hair cells) and for normal cochlear amplification (outer hair cells). The human fetus in utero is relatively hypoxic and there is evidence that its auditory threshold is also similarly elevated. Therefore the threshold elevation in the fetus in utero, estimated to be about 20 dB, is a consequence of both reduced transduction current through the inner hair cells (about 10 dB) and an additional 10 dB reduction in the activity of the cochlear amplifier of the outer hair cells.

Animals↗
PubMed1995

Chromate allergy from 'antifreeze-antiboil'.

A diesel mechanic developed hand dermatitis after more than 3 years in the trade. Patch testing showed positive reactions to chromate and cobalt. Potassium dichromate is added to antifreeze-antiboil as a corrosion inhibitor.

Adult↗
PubMed1995

Corticosteroid allergy.

Allergy to corticosteroids is becoming increasingly recognized. Diagnosis is difficult because of frequently false-negative patch tests. The optimum concentration and vehicle for patch testing with pure corticosteroid has still not been established. The patch test results of 19 patients with allergy to corticosteroids seen at the Skin and Cancer Foundation in Sydney, Australia, were analysed. It was found that patch testing with the patient's corticosteroid in the commercial cream base gave a greater yield of positive results than testing with the commercial corticosteroid ointment or with the pure corticosteroid in either petrolatum or in alcohol. Tixocortol pivalate, and to a lesser extent budesonide, were useful for detecting allergy to hydrocortisone, but not necessarily other corticosteroids. Delayed positive patch tests were often seen, showing the importance of carrying out a late reading. The repeat open application test (ROAT) with the patient's own corticosteroid was found to be a simple, useful diagnostic test.

Adrenal Cortex Hormones↗
PubMed1995

Oral lichenoid lesions caused by allergy to mercury in amalgam fillings.

Oral lichenoid lesions (OLL) or lichen-planus-like lesions are often idiopathic. Our aim was to determine whether OLL can be caused by allergy to mercury in amalgam fillings, and whether resolution of OLL occurs after replacement of amalgam with other dental fillings. Patients with only OLL (except for 1 case with cutaneous lichen planus) referred for patch testing during 1985-1994 to the Contact and Occupational Dermatitis Clinic of the Skin & Cancer Foundation, Darlinghurst, were reviewed. Patch tests were performed with 1% mercury, 1% ammoniated mercury, 0.1% thimerosal, 0.1% mercuric chloride, 0.05% phenylmercuric nitrate and an amalgam disc, using Finn Chambers occluded for 2 days, 19 patients (17 women and 2 men; age range: 28-72 years) had OLL in close contact with amalgam fillings and showed positive patch test reactions to mercury compounds, 16 out of 19 patients had their amalgam fillings replaced. In 13 patients, the OLL healed. 1 patient had marked improvement. 1 patient had no improvement and developed multiple oral squamous cell carcinoma. In conclusion, OLL can be caused by allergy to mercury in amalgam fillings. Replacement of amalgam with other dental fillings usually results in resolution of OLL and is recommended for cases with positive patch test reactions to mercury compounds.

Adult↗
PubMed1995

Water intake and activity of hypothalamoneurohypophysial system during osmotic and sodium stimulation in rats.

Intrajugular infusion (200 microliters/min for 10 min) of 0.85 M NaCl or 1.7 M mannitol in conscious adult male Sprague-Dawley rats increased plasma osmolality similarly and had an additive effect when combined. Plasma Na+ concentration, however, increased with infusion of 0.85 M NaCl, decreased with 1.7 M mannitol, and was not significantly altered by the combined solution. Irrespective of changes in plasma Na+ concentration, plasma vasopressin and oxytocin concentrations were elevated to a similar degree after independent infusion of 0.85 M NaCl or 1.7 M mannitol. With the combined infusion, the change in plasma vasopressin was additive but the change in oxytocin tended to be greater. Accordingly, glucose utilization increased throughout the hypothalamoneurohypophysial system after infusion of 0.85 M NaCl and 1.7 M mannitol. With the combined infusion, however, the change in glucose utilization in the paraventricular nucleus was additive but a synergistic effect occurred in the supraoptic nucleus and neural lobe. Drinking responses were similar in all groups receiving hypertonic solutions, with no additive effect after the combined stimulus. Although our results do not completely rule out the participation of cerebrospinal fluid sodium receptors, it is more likely that osmoreceptors regulate the activity of the hypothalamoneurohypophysial system and drinking behavior. Unlike the magnocellular system, however, drinking behavior seems to be negatively influenced by a stress component of the osmotic stimulation.

Animals↗