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1.
PLoS One ; 17(12): e0278638, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36454971

RESUMO

This study aimed to clarify the educational significance and issues associated with administering the objective structured clinical examination (OSCE) twice to midwifery students, i.e., before and after clinical training. In Sapporo City University in Japan, 37 assessment items of the OSCE were configured as "Overall," with 17 items as midwifery's normal delivery preparation (Part 1) and 20 items as midwifery's normal delivery assistance (Part 2). All students had attended lectures with textbooks. The first and second OSCEs were conducted before and after the clinical training, respectively. The scores of 54 students were retrospectively analyzed over 6 years (2014-2019). The results of the first and second OSCEs were compared. Statistical analysis was performed using Mann-Whitney U test, Wilcoxon signed rank-sum test, Fisher's exact test, and analysis of variance. The mean scores for "Overall" [0-37], "Part 1" [0-17], and "Part 2" [0-20] in the second OSCEs were significantly higher than those in the first OSCE (Overall: 22.7 vs 19.3, Part 1: 9.50 vs 7.71, Part 2: 13.2 vs 11.6, p<0.05, respectively). Regarding "Overall" and "Part 1," a positive correlation was observed between the first and second OSCEs, wherein the full scores of "Part 1," converted from 17 to 20 points to match the full scores of "Part 2," were significantly lower than those of Part 2 (p<0.05, respectively). There was a positive correlation between the scores of the first and second OSCEs in "Part 1" and "Part 2" (p<0.05). The scores increased between the two OSCEs, and participants could objectively grasp the knowledge and skills. The OSCEs conducted twice were useful in skilling-up the normal delivery preparation and assistance skills of midwifery students. However, developing an advanced educational method might be necessary for the midwifery students' preparation of normal delivery, because the scores in the OSCEs were lower.


Assuntos
Tocologia , Humanos , Gravidez , Feminino , Universidades , Japão , Estudos Retrospectivos , Estudantes
2.
BMC Endocr Disord ; 22(1): 164, 2022 Jun 22.
Artigo em Inglês | MEDLINE | ID: mdl-35733207

RESUMO

BACKGROUND: Familial hypocalciuric hypercalcemia (FHH) is a rare autosomal dominant disease, which requires differential diagnosis from relatively common primary hyperparathyroidism (PHPT) in order to avoid unnecessary surgery. CASE PRESENTATION: A 16-year-old female had been followed by the department of psychosomatic medicine at our institution. Throughout the follow-up period, her plasma calcium levels were high, plasma Pi levels were relatively low, and plasma intact PTH was relatively high. She was referred to our department to determine the cause of her hypercalcemia. Her 24 h urinary calcium excretion was as low as 100 mg/day, and calcium creatinine clearance ratio was below 0.01. Moreover, she had a family history of hypercalcemia (proband, her brother, and her father). The genetic testing for her family revealed that she, her brother, and her father were definitively diagnosed with FHH type 1 due to the heterozygous calcium-sensing receptor mutation (NM_00388:4:c.164C > T:p.Pro55Leu). CONCLUSION: We experienced a 16-year-old female with FHH, in whom genetic testing identified the heterozygous calcium-sensing receptor mutation (NM_00388:4:c.164C > T:p.Pro55Leu) as pathogenic, permitting a definitive diagnosis of FHH type 1. The genetic testing for calcium sensing receptor is beneficial to distinguish asymptomatic primary hyperparathyroidism from FHH.


Assuntos
Hipercalcemia , Hiperparatireoidismo Primário , Adolescente , Cálcio , Feminino , Humanos , Hipercalcemia/congênito , Hipercalcemia/diagnóstico , Hipercalcemia/genética , Hiperparatireoidismo Primário/diagnóstico , Hiperparatireoidismo Primário/genética , Masculino , Mutação , Receptores de Detecção de Cálcio/genética
3.
Brain Nerve ; 67(12): 1471-80, 2015 Dec.
Artigo em Japonês | MEDLINE | ID: mdl-26618761

RESUMO

Attention is the process by which information and selection occurs, the thalamus plays an important role in the selective attention of visual and auditory information. Selective attention is a conscious effort; however, it occurs subconsciously, as well. The lateral geniculate body (LGB) filters visual information before it reaches the cortex (bottom-up attention). The thalamic reticular nucleus (TRN) provides a strong inhibitory input to both the LGB and pulvinar. This regulation involves focusing a spotlight on important information, as well as inhibiting unnecessary background information. Behavioral contexts more strongly modulate activity of the TRN and pulvinar influencing feedforward and feedback information transmission between the frontal, temporal, parietal and occipital cortical areas (top-down attention). The medial geniculate body (MGB) filters auditory information the TRN inhibits the MGB. Attentional modulation occurring in the auditory pathway among the cochlea, cochlear nucleus, superior olivary complex, and inferior colliculus is more important than that of the MGB and TRN. We also discuss the attentional consequence of thalamic hemorrhage.


Assuntos
Atenção/fisiologia , Vias Auditivas/fisiologia , Núcleos Talâmicos/patologia , Tálamo/patologia , Tálamo/fisiopatologia , Vias Auditivas/fisiopatologia , Corpos Geniculados/patologia , Humanos , Neurônios/fisiologia , Tálamo/fisiologia
4.
Biosci Biotechnol Biochem ; 77(5): 992-7, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23649260

RESUMO

Colostrum is a complex mixture of bioactives that promotes neonate growth. Recently, we have found by in vivo study that skimmed, sterilized, and concentrated bovine late colostrum (SCBLC), obtained from a Holstein herd on days 6-7 after parturition, had an ability to maintain intestinal integrity. In the present study we investigated effects of SCBLC on rat intestinal IEC-6 cell proliferation in vitro. A fraction containing αs1-casein was found to have a robust stimulation effect as compared to other protein fractions from SCBLC and even the αs1-casein fraction from milk from other Holstein herds. Furthermore, the SCBLC αs1-casein molecule demonstrated not only slightly slower mobility on both SDS- and native-PAGE than other bovine milk αs1-caseins, but also a peculiar conformation reminiscent of moltenglobule in the circular dichroism spectrum. These findings may be of relevant to the competence of SCBLC to preserve intestinal integrity.


Assuntos
Caseínas/isolamento & purificação , Caseínas/farmacologia , Colostro/química , Mucosa Intestinal/citologia , Animais , Bovinos , Linhagem Celular , Proliferação de Células/efeitos dos fármacos , Feminino , Leite/química , Proteínas do Leite/farmacologia , Gravidez , Ratos , Especificidade da Espécie , Proteínas do Soro do Leite
5.
Biosci Biotechnol Biochem ; 74(3): 680-2, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20208370

RESUMO

We found that skimmed and concentrated bovine late colostrum (SCBLC) obtained from normal cows at 6-7 d after parturition exhibited high potency in inhibiting replication of human rotavirus (HRV) in vitro. Furthermore, prophylactic oral administration of SCBLC once before inoculation of HRV prevented the development of diarrhea in suckling mice in vivo. SCBLC from normal cows might be useful in the prevention of HRV-induced severe gastroenteritis in immunocompromised hosts.


Assuntos
Colostro/imunologia , Infecções por Rotavirus/prevenção & controle , Animais , Animais Lactentes , Bovinos , Diarreia/imunologia , Diarreia/prevenção & controle , Feminino , Gastroenterite/imunologia , Gastroenterite/prevenção & controle , Humanos , Camundongos , Gravidez , Rotavirus/fisiologia , Infecções por Rotavirus/imunologia , Replicação Viral
6.
Intern Med ; 43(5): 410-4, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-15206555

RESUMO

A 69-year-old woman was referred to our department for evaluation of hypokalemia, which had been treated by oral potassium for more than ten years. She complained of headache, knee joint pain, sleeplessness and paresthesia in extremities and, most prominently, depression. Laboratory data suggested Gitelman's syndrome, which is caused by mutations in the gene encoding the thiazide-sensitive Na-Cl cotransporter. Direct sequencing of the gene in this patient revealed homozygous mutation R964Q in exon 25. Intravenous supplement of MgSO4 dramatically improved both the depression and the paresthesia, suggesting that hypomagnesemia played a role in the clinical manifestations.


Assuntos
Síndrome de Bartter/diagnóstico , Transtorno Depressivo/tratamento farmacológico , Deficiência de Magnésio/prevenção & controle , Sulfato de Magnésio/administração & dosagem , Parestesia/tratamento farmacológico , Idoso , Alcalose/diagnóstico , Transtorno Depressivo/diagnóstico , Feminino , Seguimentos , Humanos , Hiperaldosteronismo/diagnóstico , Hipocalcemia/diagnóstico , Hipopotassemia/diagnóstico , Infusões Intravenosas , Deficiência de Magnésio/diagnóstico , Parestesia/diagnóstico , Medição de Risco , Síndrome , Resultado do Tratamento
7.
J Biol Chem ; 278(2): 1149-57, 2003 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-12407109

RESUMO

Previous studies showed that short term exposure of cells to high glucose destabilized protein kinase C (PKC) betaII mRNA, whereas PKCbetaI mRNA levels remained unaltered. Because PKCbeta mRNAs share common sequences other than the PKCbetaII exon encoding a different carboxyl terminus, we examined PKCbetaII mRNA for a cis-acting region that could confer glucose-induced destabilization. A beta-globin/growth hormone reporter con struct containing the PKCbetaII exon was transfected into human aorta and rat vascular smooth muscle cells (A10) to follow glucose-induced destabilization. Glucose (25 mm) exposure destabilized PKCbetaII chimeric mRNA but not control mRNA. Deletion analysis and electrophoretic mobility shift assays followed by UV cross-linking experiments demonstrated that a region introduced by inclusion of the betaII exon was required to confer destabilization. Although a cis-acting element mapped to 38 nucleotides within the betaII exon was necessary to bestow destabilization, it was not sufficient by itself to confer complete mRNA destabilization. Yet, in intact cells antisense oligonucleotides complementary to this region blocked glucose-induced destabilization. These results suggest that this region must function in context with other sequence elements created by exon inclusion involved in affecting mRNA stability. In summary, inclusion of an exon that encodes PKCbetaII mRNA introduces a cis-acting region that confers destabilization to the mRNA in response to glucose.


Assuntos
Éxons , Glucose/farmacologia , Isoenzimas/genética , Proteína Quinase C/genética , RNA Mensageiro/metabolismo , Animais , Sequência de Bases , Linhagem Celular , Globinas/genética , Meia-Vida , Dados de Sequência Molecular , Músculo Liso Vascular/citologia , Oligonucleotídeos Antissenso/farmacologia , Proteína Quinase C beta , Splicing de RNA , Ratos
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