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1.
Vaccine ; 40(39): 5651-5656, 2022 09 16.
Article in English | MEDLINE | ID: mdl-36030122

ABSTRACT

Annual influenza vaccination of health care students and workers helps protect themselves and patients from influenza, which has a high disease burden during seasonal peaks in Australia. Health care students are an important cohort whose early attitudes and habits towards influenza vaccination may influence future behaviours. We explored the knowledge, attitudes, and behaviours towards influenza vaccination of health care students in two universities from 2018 to 2020 using convergent mixed methodology. We also assessed the impact of two external events - the introduction of mandatory influenza vaccination for select students in 2019, and the COVID-19 pandemic in 2020. We found a significant increase in self-reported vaccination uptake between 2018 (73.5%) and 2020 (89.6%), with the mandate and COVID-19 pandemic being likely drivers of increased uptake. Vaccine mandates are effective but must be supported by easy accessibility, adequately addressing concerns around effectiveness and safety, and promotion of voluntary acceptance and trust.


Subject(s)
COVID-19 , Influenza Vaccines , Influenza, Human , Australia/epidemiology , COVID-19/prevention & control , Health Knowledge, Attitudes, Practice , Humans , Influenza, Human/epidemiology , Influenza, Human/prevention & control , Pandemics/prevention & control , Students , Surveys and Questionnaires , Vaccination
2.
Regul Toxicol Pharmacol ; 32(1): 127-33, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11029275

ABSTRACT

The herbicide acetochlor, and its analogue alachlor, have similar toxicological properties, the most significant being the induction of nasal adenomas in rats in 2-year feeding studies. Previous investigations have proposed a mode of action involving metabolism to a quinone-imine, the formation of protein adducts, cell death, and compensatory hyperplasia leading to the observed adenomas. Comparisons between rats and humans of the metabolic cascade leading to the quinone-imine indicate that these chemicals do not pose a threat to humans. Further investigations with acetochlor, presented here, have revealed an additional activation pathway in which a sulfoxide metabolite of acetochlor plays a key role. The sulfoxide was found to be the major plasma metabolite in rats dosed with acetochlor. Whole-body autoradiography studies established that this metabolite selectively accumulates and persists in the olfactory epithelium of rats. Radiolabeling of the sulfoxide molecule in the phenyl ring and in the sulfoxide side-chain demonstrated that the metabolite accumulating in nasal tissues retains the sulfoxide side-chain. The formation of a quinone-imine from the sulfoxide was facilitated by hydroxylation of the phenyl ring by a cytochrome P450 isoenzyme which was specific to the nasal epithelium in the rat. This metabolic conversion could not be detected in 33 fresh human nasal tissue samples, supporting the earlier view that the acetochlor-induced rat nasal tumors do not represent a hazard for humans.


Subject(s)
Aryl Hydrocarbon Hydroxylases , Herbicides/pharmacokinetics , Nose Neoplasms , Toluidines/pharmacokinetics , Adenoma/chemically induced , Adenoma/pathology , Animals , Autoradiography , Cytochrome P-450 CYP2A6 , Cytochrome P-450 Enzyme System/metabolism , Herbicides/toxicity , Humans , Liver/drug effects , Liver/metabolism , Male , Mice , Mice, Inbred Strains , Microsomes/drug effects , Microsomes/metabolism , Mixed Function Oxygenases/metabolism , Nose Neoplasms/chemically induced , Nose Neoplasms/pathology , Olfactory Mucosa/drug effects , Olfactory Mucosa/enzymology , Rats , Rats, Sprague-Dawley , Species Specificity , Toluidines/toxicity
3.
J Lab Clin Med ; 135(2): 170-3, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10695662

ABSTRACT

To assess the prevalence of mutations in the HFE (hemochromatosis) gene in unselected male patients with type 2 diabetes, we examined 220 white men without known diabetes and 220 age-matched white men with type 2 diabetes for mutations in the HFE gene. Nucleotide 845 (C282Y) and 187(H63D) alleles were amplified by polymerase chain reaction (PCR) with lymphocyte DNA. The PCR products were analyzed by restriction enzyme digestion. One of the 220 patients (0.45%) with diabetes was homozygous for the HFE 845A (C282Y) mutation and 25 (11.3%) were heterozygous for the same mutation, of whom 3 (1.3%) were compound heterozygotes also carrying the HFE 187G (H63D) mutation. These frequencies did not differ significantly from the control population without diabetes. There is no evidence that HFE mutations are found in excess in unselected male patients with type 2 diabetes, and there is no indication for a population-based search for an excess of these alleles in type 2 diabetes.


Subject(s)
Diabetes Mellitus, Type 2/genetics , HLA Antigens/genetics , Hemochromatosis/genetics , Histocompatibility Antigens Class I/genetics , Membrane Proteins , Point Mutation , Adult , Aged , Alleles , Amino Acid Substitution , DNA/blood , Diabetes Mellitus, Type 2/blood , England , Ferritins/blood , Hemochromatosis Protein , Heterozygote , Homozygote , Humans , Iron/blood , Lymphocytes/blood , Male , Middle Aged , Polymerase Chain Reaction , White People
4.
Hum Exp Toxicol ; 15(9): 702-35, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8880207

ABSTRACT

Comprehensive toxicological studies of the herbicide acetochlor are presented and discussed. Although it gave a negative profile of responses in the many toxicity tests conducted there were some findings that prompted further investigation. First, although non-mutagenic in the Salmonella assay, acetochlor was clastogenic to mammalian cells treated in vitro. This clastogenic potential was not expressed in vivo in four rodent cytogenetic assays (bone marrow and germ cells). Second, although acetochlor gave a negative response in rat liver UDS assays when tested at the acute MTD, gavage administration of a single, supra-MTD dose (2000 mg/kg) gave a weak positive assay response. This dose-level (2000 mg/kg) was necrotic to the liver, depressed hepatic glutathione levels by up to approximately 80%, altered the metabolism of acetochlor, and was associated with up to 33% lethality. In contrast, reference liver genotoxins such as DMN, DMH and 2AAF were shown to elicit UDS in the absence of such effects, and at approximately 400 x lower dose-levels. Finally, microscopic nasal polypoid adenomas were induced in the rat when acetochlor was administered for two years at the maximum tolerated dose (MTD). The tumours were not life-threatening, they did not metastasize, and no DNA damage was induced in the nasal cells of rats maintained on a diet containing the MTD of acetochlor for either 1 or 18 weeks (comet assay). In order to probe the mechanism of action of these high dose toxicities a series of chemical and genetic toxicity studies was conducted on acetochlor and a range of structural analogues. These revealed the chloroacetyl substructure to be the clastogenic species in vitro. Although relatively inert, this substituent is preferentially reactive to sulphydryl groupings, most evidently, to glutathione (GSH). Similar chemical reactivity and clastogenicity in vitro was observed for two related chemicals bearing a chloroacetyl group, both of which have been defined as non-carcinogens in studies reported by the US.NTP. These collective observations indicate that the source of the clastogenicity of acetochlor in vitro is also the source of its rapid detoxification in the rat in vivo, via reaction with GSH. Metabolic studies of acetochlor are described which reveal the formation of a series of GSH-associated biliary metabolites in the rat that were not produced in the mouse. The metabolism of acetochlor in the rat changes with increasing dose-levels, probably because of depletion of hepatic GSH. It is most likely that a rat-specific metabolite is responsible for the rat nasal tumours observed uniquely at elevated dose-levels. The absence of genetic toxicity to the nasal epithelium of rats exposed acutely or subchronically to acetochlor favours a non-genotoxic mechanism for the induction of these adenomas. The observation of a time- and dose-related increase in S-phase cells in the nasal epithelium is consistent with this conclusion. Despite some confusion caused by the early use of perilethal gavage administrations of acetochlor to rodents, and supra-MTD dietary concentrations in some of the chronic studies, the available MTD data are consistent with acetochlor not posing a genetic or carcinogenic hazard to humans.


Subject(s)
Bone Marrow/drug effects , Carcinogens/toxicity , Germ Cells/drug effects , Herbicides/adverse effects , Toluidines/adverse effects , Adenomatous Polyps/chemically induced , Adenomatous Polyps/pathology , Adenomatous Polyps/ultrastructure , Administration, Oral , Animals , Bone Marrow Cells , Chromatography, High Pressure Liquid , DNA Damage/drug effects , Disease Models, Animal , Dose-Response Relationship, Drug , Epithelial Cells , Epithelium/drug effects , Female , Germ Cells/cytology , Glutathione/metabolism , Herbicides/administration & dosage , Humans , Liver/cytology , Liver/drug effects , Liver Cirrhosis, Experimental/chemically induced , Liver Cirrhosis, Experimental/mortality , Male , Mice , Mice, Inbred C57BL , Mutagenicity Tests , Nasal Polyps/chemically induced , Nasal Polyps/pathology , Nasal Polyps/ultrastructure , Rats , Rats, Sprague-Dawley , Reproduction/drug effects , Sulfhydryl Reagents/toxicity , T-Lymphocytes , Toluidines/administration & dosage
5.
CMAJ ; 149(2): 139, 1993 Jul 15.
Article in English | MEDLINE | ID: mdl-8324708
6.
CMAJ ; 139(1): 11-2, 1988 Jul 01.
Article in English | MEDLINE | ID: mdl-3383031
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