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R S Jones

Publications and source records attributed to R S Jones.

At least 73 records · Page 4Linked to original sources

The Drosophila Enhancer of zeste gene encodes a chromosomal protein: examination of wild-type and mutant protein distribution.

The Drosophila Enhancer of zeste [E(z)] gene is a member of the Polycomb-group and, as such, is involved in maintaining the transcriptional repression of the homeotic genes of the Antennapedia (ANT-C) and bithorax (BX-C) complexes. It has been proposed that Polycomb-group (Pc-G)-mediated silencing requires the formation of heteromeric protein complexes which modify the chromatin structure of target genes. We describe the in vivo distribution of the E(Z) protein and show it to be ubiquitously present in embryonic and larval nuclei. In salivary gland polytenized nuclei, the identifiable E(Z) chromosome binding sites are a subset of those described for other Polycomb-group proteins, suggesting that E(Z) may also participate in Polycomb-group complexes. E(Z) binds to chromosomes in a DNA sequence-dependent manner, as illustrated by the creation of a new E(Z)-binding site at the location of a P element reporter construct that previously has been shown to contain a Polycomb response element (PRE). We also present the sequences of one null and three temperature-sensitive E(z) alleles, describe the effects these mutations have on the in vivo distribution of E(Z) protein and discuss their implications concerning putative functional domains. Finally, we describe the effect a trithorax mutation has on E(Z) chromosome binding.

Animals↗

Simultaneous open reduction and Salter innominate osteotomy for developmental dysplasia of the hip.

We have studied retrospectively 37 hips in 36 children at an average of 91 months after simultaneous open reduction and Salter innominate osteotomy for developmental hip dysplasia. At the latest review 97.3% were clinically and 83.8% radiologically good or excellent. In three hips (8%) there were signs of avascular necrosis, but only one had been symptomatic. There were no cases of recurrent posterior displacement.

Age Factors↗

Genotoxicity studies of quercetin and shikimate in vivo in the bone marrow of mice and gastric mucosal cells of rats.

Bracken fern (Pteridium aquilinum) causes acute and chronic toxicity in animals and is associated with a high incidence of stomach and esophageal tumors in humans in countries where it is consumed as food, yet the toxic constituent(s) has not been unequivocally identified. None of the toxic constituents so far isolated from bracken have individually reproduced all the disease syndromes typical of the plant. The carcinogenicity of the plant has at one time or another been attributed to quercetin, shikimate or ptaquiloside. Studies to determine whether or not the genotoxicity of quercetin, shikimate (and its metabolite cyclohexane-carboxylate) could be enhanced in combined application were conducted in vivo using the micronucleus test in mice and the unscheduled DNA synthesis in rat gastric mucosal cells. None of these compounds were genotoxic; simultaneous administration of the compounds did not influence their in vivo genotoxicity. Plasma concentrations of quercetin after p.o. and i.p. administration at 200 mg/kg were below 0.1 microgram/ml, suggesting that the negative in vivo results may have been due to limited bioavailability of the compound.

Animals↗

Cytotoxicity studies of quercetin, shikimate, cyclohexanecarboxylate and ptaquiloside.

A study was carried out to determine the cytotoxic effects of quercetin, shikimate, cyclohexane-carboxylate and ptaquiloside on Chinese hamster ovary (CHO), mouse fibroblast (3T3) and normal rat kidney (NRK) cells by cell growth inhibition assay of monolayers grown in 96-well plates. Molar concentrations inhibiting cell growth by 50% (IC50) after 48 h of incubation for quercetin, shikimate, cyclohexanecarboxylate and ptaquiloside were 0.8 x 10(-4)M, 0.8 x 10(-3)M, 0.4 x 10(-2) M and 0.6 x 10(-1)M respectively for CHO cells; 1.2 x 10(-4)M, 0.7 x 10(-3)M, 0.2 x 10(-7)M and 0.6 x 10(-1)M respectively for 3T3 cells; and 0.7 x 10(-4)M, 1.0 x 10(-3)M, 0.2 x 10(-2)M and 0.6 x 10(-1)M respectively for NRK cells. These inhibiting concentrations were extremely high when compared with mitomycin C whose cytotoxic effect occurred at 1 x 10(-6)M. Cyclohexanecarboxylate is a metabolite of shikimate; any possible cytotoxic effect of shikimate in vivo may be mediated by the major metabolite cyclohexanecarboxylate per se or after futher metabolism of this metabolite following absorption in animals. Quercetin, ptaquiloside and shikimate are constituents of bracken fern. The low order of cytotoxic activity of these constituents suggest that they are probably not directly the etiological agents of acute cattle bracken fern poisoning.

Animals↗

Mechanical properties of the human anterior cruciate ligament.

The aim was to measure the stiffness and strength of the femur-anterior cruciate ligament-tibia complex tested in a physiological manner with a force exerted anteriorly on the tibia, at knee joint flexion angles of 0 degrees, 10 degrees and 30 degrees and at speeds of 50 and 500 mm/min. Ligaments were preconditioned by cycling five times, with data from the fifth cycle used to determine the stiffness of the ligament in a low-load range. The ligaments were then tested to failure with the knee at 30 degrees flexion. The specimens were divided into two groups, middle-aged (40-60) and old (>60). For each group no statistical difference was observed between stiffness of the ligament at different joint flexion angles or speeds. Seven of the 21 specimens in the older age group failed by avulsion at the bone-ligament interface. All the other specimens failed by tears in the substance of the ligament. Ultimate failure load was found to have a significant correlation with bodyweight. It was 1.6 and 1.3 times bodyweight for the middle-aged and older age groups respectively. This study has highlighted the importance of identifying different modes of failure, of making corrections for bodyweight and testing in a physiological manner. The results allow a better understanding of the mechanical behaviour of the anterior cruciate ligament and provide design data for anterior cruciate ligament grafts and prostheses. RELEVANCE:--Our clinical experience indicates that the anterior cruciate ligament is frequently ruptured during uncoordinated contraction of the quadriceps mechanism. The results of this study, in which the mechanical properties of the anterior cruciate ligament have been measured with force exerted anteriorly on the tibia, allow a more complete understanding of the mechanical behaviour of the anterior cruciate ligament and provide design data for anterior cruciate ligament grafts and prostheses.

Journal Article↗

Study of rat liver transplantation from non-heartbeating cadaver donors.

BACKGROUND: The aim of this study was to determine if livers could tolerate prolonged warm ischemia and to determine optimum timing of intervention in the cadaver donor to preserve liver viability. Livers harvested from non-heartbeating donors (NHBDs) would greatly expand the donor pool for transplantation. However, sensitivity of the donor liver to warm ischemia is a major obstacle for successful use of livers from NHBDs. The limit of non-heartbeating time in the donor remains unknown. STUDY DESIGN: Hepatic transplantation was performed in ten groups of rats with stepwise increase of cardiac arrest time in the donor from zero to 180 minutes with 20-minute intervals. The cardiac arrest time was counted from ligation of the base of the donor's heart to the beginning of cold flushing of the liver. Bile flow, bile acid outputs, hepatic functions, and rat survival rates in each group were compared. RESULTS: Survival rates from groups 1 to 10 were 83.3, 100, 83.3, 50, 66.7, 50, 16.7, 16.7, zero, and zero percent, respectively. The stepwise increase of non-heartbeating time significantly reduced recipient survival rates after 100 minutes. In addition, the increase caused a stepwise decrease of bile flow rates and bile salt outputs and an increase of serum aspartate aminotransferase and lactate dehydrogenase activities. CONCLUSIONS: The liver is less sensitive to warm ischemia than formerly believed. Rat livers can be used for transplantation after cardiac arrest up to 140 minutes with a chance of survival.

Animals↗

The biopsy of hepatobiliary and pancreatic masses.

Neoplasms of the liver, biliary structure, and pancreas often provide a challenge for diagnosis and management. The techniques employed currently for sampling cells or tissues preoperatively and intraoperatively can provide information to assist the surgeon in planning therapy. This article discusses the use and effectiveness of biopsy techniques.

Ampulla of Vater↗

Multiparameter digital image analysis of biliary, ampullary, and pancreatic adenocarcinomas.

Periampullary adenocarcinomas arise from pancreatic, biliary, or ampullary ductal epithelium. Their origin is difficult or impossible to discern by routine light microscopy of cytologic or small biopsy specimens. We used image analysis to describe the morphologic features of Feulgen-stained nuclei of biliary and ampullary adenocarcinomas and to compare these findings with those of pancreatic ductal adenocarcinomas. Surgically resected cases of ampullary adenocarcinoma (n = 7) and cholangiocarcinoma (n = 26) were selected on the basis of available formalin-fixed, paraffin-embedded tissue and diagnostic clinical data. Disaggregated nuclei were stained by the Feulgen reaction and analyzed using a digital image processor. Data from 15 morphonuclear parameters were assessed and compared with the results from the morphonuclear analysis of 22 pancreatic ductal adenocarcinomas. Multivariate analysis with canonical transformation of the data defined the ampullary adenocarcinomas and cholangiocarcinomas as occupying similar factorial distributions, whereas the pancreatic carcinomas were separate and distinct. Monovariate analysis identified seven parameters distinguishing pancreatic carcinoma from both ampullary carcinoma and cholangiocarcinoma, with P values < or = 0.001 and two others having P values < or = 0.01. Adenocarcinomas of ampullary or bile duct origin possess similar morphonuclear features described by image analysis. Image analysis provides a mechanism to discriminate adenocarcinomas arising from the bile ducts or ampulla from those arising in the pancreas.

Adenocarcinoma↗

Humane destruction of horses with a mixture of quinalbarbitone and cinchocaine.

One hundred and-two horses requiring to be euthanased for a variety of reasons were killed by the intravenous injection of a mixture of quinalbarbitone sodium (400 mg/ml) and cinchocaine hydrochloride (25 mg/ml). The dose rates used were 1 ml/10, 15, 20 and 30 kg bodyweight, and the time of injection was varied between 5 and 25 seconds. The average time to collapse from the start of the injection was 34 seconds and the average time to clinical death was 230 seconds. Slow injection (particularly of the low dose rates) and premedication with detomidine resulted in a longer time to collapse (median 46 seconds). Premedication with xylazine and low dose rates of the mixture resulted in an unacceptable degree of muscular activity and agonal gasping and death was delayed. Premedication with romifidine and butorphanol resulted in an apparent (but insignificant) reduction in the time to collapse and death but was also accompanied by significant agonal gasping. Without premedication quinalbarbitone and cinchocaine resulted in a smooth and quiet collapse with the cessation of cardiac and respiratory functions within three minutes in all cases, but the palpebral reflex of the horses was prolonged significantly beyond the time when all other reflex activity was lost. Occasional gasping and muscular tremors, particularly of the upper forelimb, occurred particularly when lower dose rates and either very slow or very fast rates of injection were used. One horse which was premedicated with xylazine and received a very low dose at a slow rate showed unacceptably violent muscular activity. At no other time was the procedure regarded as violent or unacceptable.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Welfare↗

Direct projections from the ventrolateral medulla oblongata to the limbic forebrain: anterograde and retrograde tract-tracing studies in the rat.

Neurons in the ventrolateral medulla oblongata, a brain region implicated in central vasomotor regulation, have previously been reported to project to some forebrain limbic structures. The aim of the present study was (1) to describe the termination pattern of ventral medullary afferents in forebrain limbic areas using anterograde tract tracing, and (2) to determine the location and some morphological characteristics of the projection neurons using retrograde tract tracing from selected forebrain sites. Following ionophoretic microinjections of the anterograde tract tracer Phaseolus vulgaris leucoagglutinin into the rostral ventrolateral medulla, labelled afferents were observed in the hippocampus, entorhinal and retrosplenial cortices, dorsal septum, nucleus accumbens, and the medial prefrontal cortex. Anterogradely labelled axons, ascending from the caudal ventrolateral medulla, could be traced only to the rostral aspects of the investigated forebrain limbic structures. Here, the main target of the ascending projection was in the ventral septum. However, labelled terminals were also present in the nucleus accumbens, the dorsolateral septum, and in the infralimbic cortex. The density of the ventrolateral medullary projections into all examined forebrain areas was low. The location of the cells in the ventral medulla oblongata which give rise to direct forebrain projections was examined using retrograde tract tracing with wheat germ agglutinin conjugated horseradish peroxidase (WGA-HRP). Following WGA-HRP injections into the septo-accumbens region, retrogradely labelled cells were present in both the rostral and caudal ventrolateral medulla. When the tract tracer injection was restricted to the ventral region of the septal complex, the labelled cells were concentrated in the caudal aspects of the ventrolateral medulla (and the nucleus of the solitary tract). Following tracer injections into the anterior cingulate cortex or the hippocampus or the entorhinal cortex, retrogradely labelled cells in the medulla oblongata were predominantly in the rostral ventrolateral medulla. As a first attempt to reveal the chemical nature of the projection cells, the contribution of tyrosine hydroxylase-immunoreactive cells to the innervation of the septo-accumbens area was also investigated: tyrosine hydroxylase-immunoreactive cells of both the caudal ventrolateral medulla and the nucleus of the solitary tract were found to contribute to the innervation of the septo-accumbens area. The distribution of retrogradely labelled cells as well as the termination pattern of the anterogradely labelled terminals indicated that the innervation of the various forebrain limbic areas arises from cells, diffusely distributed in the rostral and/or the caudal ventrolateral medulla oblongata.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Synaptic and intrinsic properties of neurons of origin of the perforant path in layer II of the rat entorhinal cortex in vitro.

Layer II of the entorhinal cortex (EC) provides the first step in the hippocampal trisynaptic loop via the perforant path projection to the dentate gyrus. While a great deal is known about this projection and the properties of the dentate granule cells, much less information is available concerning the properties of and synaptic inputs to the cells of origin of the pathway in layer II. The present experiments have employed a slice preparation of the rat EC to study the intrinsic membrane properties and synaptic organization of layer II neurons. Two types of neurons could be identified electrophysiologically. The majority were designated type I and displayed a pronounced time-dependent inward rectification in the hyperpolarizing direction. Type II displayed little evidence of this characteristic. However, morphological examination suggested that both types were spiny stellate neurons projecting via the perforant path. Synaptic responses of both types displayed evidence of excitatory inputs mediated by both N-methyl-D-aspartate (NMDA) and non-NMDA glutamate receptors. In general, however, at low frequencies the responses were dominated by inhibitory inputs mediated by both GABAA and GABAB receptors. At higher frequencies the bias was shifted much more toward excitation. The contribution of synaptic and intrinsic properties of layer II neurons to the processing capabilities of the EC is discussed.

Animals↗

Study of donor-recipient liver size match for transplantation.

OBJECTIVE: This animal experiment investigated the donor-recipient liver size match for safe liver transplantation. BACKGROUND: In spite of refinements in surgical techniques in reduced liver transplantation, the liver size disparity remains one of the most common complications in pediatric patients. Optimal size matching remains unknown. METHODS: The experiment compared eight groups of liver-transplanted rats with designated ratios of donor and recipient liver weights. Donor livers harvested from rats weighing 420-520 g were reduced to the designated size by liver lobectomy and implanted in rats weighing 170-240 g. Bile secretion and serum aspartate aminotransferase (AST) activities in groups 2, 4, and 6 were studied after surgery. RESULTS: Stepwise increase of the ratio of donor and recipient liver weights from 1.04:1 in group 4 to 1.26:1 in group 3, 1.56:1 in group 2, and 2.04:1 in group 1 caused stepwise decrease of survival rates from 83.3% to 66.7%, 16.7%, and 0%, respectively. Stepwise decrease of the ratio from 1.04:1 in group 4 to 0.79:1 in group 5, 0.53:1 in group 6, 0.35:1 in group 7, and 0.24:1 in group 8 also caused stepwise reduction of survival rates from 83.3% to 66.7%, 50%, 0%, and 0% in each group. CONCLUSION: The range of ratios of donor and recipient liver weights for successful rat liver transplantation is from 0.53:1 to 1.26:1. Increase and decrease of ratios of donor-recipient liver weights from equal size do not increase the recipient survival rates. Recipients of reduced donor liver weights tend to have a higher survival rate than recipients of increased donor liver weights.

Animals↗

Prostaglandin E1 increases survival with extended anhepatic phase during liver transplantation.

OBJECTIVE: The authors investigated the intraoperative treatment effects of Prostaglandin E1 (PGE1) for extension of the anhepatic phase and improvement of survival in a rat liver transplant model. BACKGROUND: Cross-clamping the inferior vena cava and the portal vein during liver transplantation causes severe pathophysiologic changes during surgery. The time of the anhepatic phase is strictly limited and results in a very tenuous period during the liver transplant operation. METHODS: Prostaglandin E1 was infused at 0.5 microgram/kg/min into five subgroups of rats with 20, 30, 40, 60, and 80 minutes of anhepatic phase during transplantation. Bile secretion, serum aspartate transaminase (AST), lactic dehydrogenase (LDH), and blood gas analysis were studied in the 30-minute subgroup. The results were compared with the sham-operated and control groups. RESULTS: Intraoperative treatment with PGE1 extended the maximal anhepatic phase from 30 minutes in the sham-operated group up to 80 minutes, and increased survival. Significant changes in the PGE1 treated rats in the 30-minute subgroup included an increase of bile flow and bile salt output and decrease of AST and LDH activities after surgery. Blood gas analysis showed a decrease in acidosis and hypercarbia at the end of the anhepatic phase. CONCLUSIONS: The PGE1 treatment increased survival with extended anhepatic phase during rat liver transplantation. The beneficial effects can be attributed to its biologic activities.

Alprostadil↗