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1.
BMC Med Educ ; 22(1): 408, 2022 May 27.
Article in English | MEDLINE | ID: mdl-35624492

ABSTRACT

BACKGROUND: Interprofessional collaborative practice competency (ICPC) is key to providing safe, high-quality, accessible, patient-centred care. Effective delirium management, particularly, requires a multi-component intervention, including the use of interprofessional teams at care point. This research aims to investigate the effectiveness of the flipped classroom approach for improving ICPC in simulation-based delirium case management. METHOD: An embedded mixed-methods study was designed to investigate the effects of the flipped classroom approach on health professionals' performance in delirium management. The study population comprised nine health professionals (three physicians, nurses, and pharmacists each). They used pre-class study materials about delirium management via a digital learning platform before a simulation case training session. A readiness assurance process test was conducted on key concepts, covered in the pre-class study material. Participants were randomly assigned to three teams, each of which included health professionals. Each team participated in a simulation case scenario. For the quantitative outcome measures, the Chiba Interprofessional Competency Scale (CICS29), a validated scale for measuring competencies of interprofessional practice, was used before, after, and three months after the educational intervention. The qualitative component consisted of a post-training questionnaire and semi-structured focused group interviews about the impact of the flipped classroom approach. RESULT: The CICS29 measured after the intervention and three months after was noted to be significantly higher than before the intervention. Three semi-structured focused group interviews were conducted (n=9), which, upon analysis revealed that the flipped classroom approach effected on four stages of Bloom's taxonomy level. A total of nine categories and 17 subcategories were identified corresponding to four levels of the revised Bloom's taxonomy: remember (1), understand (12), apply (23), and analyse (3). CONCLUSION: The simulation-based skill training using flipped classroom approach can be an effective method for improving ICPC for health professionals. In this approach, an elevated level of cognitive activity is practiced in the Bloom's taxonomy, and the participants worked on an application-based case simulation that promoted higher level learning and engagement in interprofessional collaborative practice. This approach also established a basic common language of delirium assessment and management, thus facilitating communication among health professionals and improving ICPC.


Subject(s)
Delirium , Physicians , Simulation Training , Delirium/therapy , Health Personnel , Humans , Surveys and Questionnaires
2.
BMC Genet ; 15: 151, 2014 Dec 20.
Article in English | MEDLINE | ID: mdl-25526961

ABSTRACT

BACKGROUND: This study investigated whether polymorphisms of the ankyrin repeat and kinase domain containing 1 gene (ANKK1), which is adjacent to the dopamine D2 receptor gene (DRD2), and the dopamine transporter (SLC6A3) and cytochrome P450 2A6 (CYP2A6) genes influence smoking cessation and nicotine dependence in a Japanese population. In 96 current and former smokers, genotyping frequencies for the ANKK1/DRD2 TaqIA, SLC6A3 VNTR, and CYP2A6 polymorphisms were subjected to chi-square analysis, and regression analyses were used to determine the association of the genotypes of current smokers with a Heavy Smoking Index, in addition to evaluating the effect of the subjects' smoking history on the association. RESULTS: Genotyping results suggested that nicotine dependence among current smokers homozygous for the SLC6A3 10r allele was lower than that of smokers carrying the minor alleles, and that the CYP2A6 polymorphism might mediate this association. Furthermore, the age at which current smokers began smoking might moderate the association between their genetic polymorphisms and nicotine dependence. CONCLUSIONS: This study provides preliminary findings on the influence of genetic variants on the smoking phenotypes in a Japanese population.


Subject(s)
Cytochrome P-450 CYP2A6/genetics , Dopamine Plasma Membrane Transport Proteins/genetics , Nicotine/metabolism , Receptors, Dopamine D2/genetics , Smoking Cessation , Tobacco Use Disorder/genetics , Adult , Female , Gene Frequency , Genetic Association Studies , Genetic Predisposition to Disease , Humans , Japan , Male , Middle Aged , Minisatellite Repeats , Polymorphism, Genetic , Protein Serine-Threonine Kinases/genetics
3.
Asian J Psychiatr ; 67: 102918, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34798384

ABSTRACT

Although many screening tools for delirium are available, delirium is still occasionally overlooked or misdiagnosed. One of the reasons for this is the lack of brief screening tools that do not require specialized training to use. The 4 'A's test (the 4AT) is a validated screening tool for delirium that can be administered in a very short time without specialized training. Herein, we evaluated the reliability and validity of the Japanese version of the 4AT (the 4AT-J). A total of 150 patients aged ≥ 65 years were enrolled. Their demographics and clinical characteristics were obtained within 24 hr of their hospitalization. On each patient's high-risk day of developing delirium, the 4AT-J was administered by a nurse, and the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-Ⅴ) and the Japanese version of Delirium Rating Scale-Revised-98 (DRS-98-J) were administered by a psychiatrist. Our analyses revealed that when a cut-off score of 4, the 4AT-J showed high sensitivity and specificity. The Cronbach's α-coefficient was similar to that of the original version. A receiver operating curve analysis showed sufficient power of the 4AT-J to discriminate delirium. The 4AT-J showed adequate reliability and validity for delirium screening in elderly patients.


Subject(s)
Delirium , Aged , Delirium/diagnosis , Geriatric Assessment , Humans , Japan , Prospective Studies , Reproducibility of Results , Sensitivity and Specificity
4.
Sci Rep ; 12(1): 8520, 2022 05 20.
Article in English | MEDLINE | ID: mdl-35595810

ABSTRACT

Breast-conserving surgery has become the preferred treatment method for breast cancer. Surgical margin assessment is performed during surgery, as it can reduce local recurrence in the preserved breast. Development of reliable and lower-cost ex vivo cancer detection methods would offer several benefits for patient care. Here, a practical and quantitative evaluation method for the ex vivo fluorescent diagnosis of breast lesions was developed and confirmed through a three-step clinical study. Gamma-glutamyl-hydroxymethyl rhodamine green (gGlu-HMRG) has been reported to generate fluorescence in breast lesions. Using this probe, we constructed a reliable and reproducible procedure for the quantitative evaluation of fluorescence levels. We evaluated the reliability of the method by considering reproducibility, temperature sensitivity, and the effects of other clinicopathological factors. The results suggest that the fluorescence increase of gGlu-HMRG is a good indicator of the malignancy of breast lesions. However, the distributions overlapped. A 5 min reaction with this probe could be used to distinguish at least part of the normal breast tissue. This method did not affect the final pathological examination. In summary, our results indicate that the methods developed in this study may serve as a feasible intraoperative negative-margin assessment tool during breast-conserving surgery.


Subject(s)
Breast Neoplasms , Margins of Excision , Breast Neoplasms/diagnostic imaging , Breast Neoplasms/surgery , Female , Fluorescent Dyes , Humans , Mastectomy, Segmental , Reproducibility of Results , gamma-Glutamyltransferase
5.
Biol Pharm Bull ; 33(6): 1060-2, 2010.
Article in English | MEDLINE | ID: mdl-20522978

ABSTRACT

We investigated the effect of ammonium vanadate (vanadate) on ATP-induced increases in intracellular calcium ion level ([Ca(2+)](i)) of human umbilical vein endothelial cells (HUVEC) by fluorescence confocal microscopic imaging using the Ca(2+)-sensitive probe Calcium Green 1/AM. The ATP analogue 2-methylthio-ATP (2meS-ATP), at 10 microM, significantly increased the [Ca(2+)](i) of HUVEC, and this was abolished by 1 microM thapsigargin (a calcium pump inhibitor), whereas extracellular free calcium had no effect. Vanadate at 10 microM also significantly increased the [Ca(2+)](i) of HUVEC, which was abolished by 1 microM thapsigargin. However, vanadate at 1 microM did not exert such a significant effect. We thus examined the influence of < or =1 microM vanadate for 24 h on 2meS-ATP-induced increase in [Ca(2+)](i). Vanadate significantly reduced the action of 2meS-ATP at 1 microM but not at 0.1 microM. Endogenously released ATP is known to induce various actions on endothelial cells. The present results suggest that vanadate exerts a regulatory influence on the function of vascular endothelial cells.


Subject(s)
Adenosine Triphosphate/metabolism , Calcium/metabolism , Endothelial Cells/metabolism , Endothelium, Vascular/drug effects , Vanadates/pharmacology , Adenosine Triphosphate/analogs & derivatives , Adenosine Triphosphate/pharmacology , Endothelial Cells/drug effects , Endothelium, Vascular/metabolism , Humans , Thapsigargin/pharmacology , Thionucleotides/pharmacology , Umbilical Veins
6.
Case Rep Obstet Gynecol ; 2019: 3929647, 2019.
Article in English | MEDLINE | ID: mdl-31934475

ABSTRACT

The patient is a 74-year-old female previously diagnosed with an ovarian tumor at age 55. No changes were noted for one year; however, she was lost to follow-up. Eighteen years later, she presented to a local clinic complaining of diffuse abdominal and flank pain. Abdominal and pelvic ultrasound, CT, and gynecological examination showed a fatty pelvic tumor of approximately 12 cm in diameter. A left ovarian teratoma was suspected, and per the patient's request, she was transferred to Kobe Adventist Hospital for further evaluation and treatment. Pelvic MRI revealed no ovarian enlargement; however, a mass in the uterine body was appreciated with a high signal on T1 and T2 images and signal dropout in the fat suppression images, a finding most consistent with a uterine lipoma. A total hysterectomy and bilateral salpingo-oophorectomy was performed, and histopathological examination confirmed the preliminary diagnosis. No complications were observed during the postoperative period. A pure uterine lipoma is an extremely rare tumor with only a few cases reported worldwide. It is a benign tumor; however, it can sometimes be misdiagnosed as a malignant neoplasm. Pelvic MRI appears to be a useful tool in order to make the correct diagnosis preoperatively.

7.
Int Urol Nephrol ; 40(1): 79-84, 2008.
Article in English | MEDLINE | ID: mdl-17619164

ABSTRACT

UNLABELLED: We assessed the potential clinical utility of levels of p53-specific antibodies as a novel serum biomarker of prostate cancer that could be used in conjunction with level of PSA. MATERIAL AND METHODS: Serum levels of p53-specific antibodies in patients with relapsed, newly diagnosed prostate cancer and in patients with benign prostate hyperplasia were quantified by an enzyme-linked immunoabsorbent assay. RESULT: There was no significant difference (P=0.96) between the serum levels of p53-specific antibodies in patients with newly diagnosed prostate cancer and with benign prostatic hyperplasia. In the newly diagnosed prostate cancer group, stage T1c (n=8) showed the lowest p53-specific antibody level. However, the difference between T1c group and benign prostatic hyperplasia group was not significant (P=0.686). The relapsed cancer group tended to have low levels of the antibodies, and, there was no significant difference between the relapsed prostate cancer group and the benign prostatic hyperplasia group (P=0.14). The serum levels of p53-specific antibodies in patients with metastatic and with localized prostate cancer showed no significant difference (P=0.68). CONCLUSION: The use of titers of p53-specific antibodies to make differential diagnosis between prostate cancer and benign prostatic hyperplasia might have no role, and the antibodies should not be used as a marker of prostate cancer by itself. Because our study is based on small number of patients, further studies are necessary before its absolute validity can be determined.


Subject(s)
Antibodies, Neoplasm/blood , Biomarkers, Tumor/blood , Prostatic Neoplasms/blood , Tumor Suppressor Protein p53/immunology , Aged , Humans , Male , Prostatic Hyperplasia/blood , Prostatic Neoplasms/immunology , Recurrence
8.
Life Sci ; 78(11): 1187-96, 2006 Feb 09.
Article in English | MEDLINE | ID: mdl-16188278

ABSTRACT

Metabolic syndrome is a cluster of metabolic abnormalities, including hypertension, hyperlipidemia, hyperinsulinemia, glucose intolerance and obesity. In such lifestyle-related diseases, impairment of nitric oxide (NO) production or bioactivity has been reported to lead to the development of atherogenic vascular diseases. Therefore, in the present study we investigated changes in the NO/cyclic guanosine monophosphate (cGMP) system in aortas of SHR/NDmcr-cp (cp/cp) rats (SHR-cp), a model of the metabolic syndrome. In aortas of SHR-cp, endothelium-dependent relaxations induced by acetylcholine and endothelium-independent relaxations induced by sodium nitroprusside were significantly impaired in comparison with Wistar-Kyoto rats. Furthermore, protein levels of soluble guanylyl cyclase and cGMP levels induced by sodium nitroprusside were significantly decreased. In contrast, protein levels of endothelium NO synthase and cGMP levels induced by acetylcholine were significantly increased, and plasma NO2 plus NO3 levels were also increased. The levels of lipid peroxide in plasma and the contents of 3-nitrotyrosine, a biomarker of peroxynitrite, in aortas were markedly increased. These findings indicate that in the aortas of SHR-cp, NO production from the endothelium is augmented, although the NO-induced relaxation response is impaired. Enhanced NO production may be a compensatory response to a variety of factors, including increases in oxidative stress.


Subject(s)
Aorta, Thoracic/metabolism , Cyclic GMP/metabolism , Metabolic Syndrome/metabolism , Nitric Oxide/metabolism , Acetylcholine/pharmacology , Animals , Aorta, Thoracic/drug effects , Blood Glucose/analysis , Blood Pressure/drug effects , Blood Pressure/physiology , Disease Models, Animal , Endothelium, Vascular/drug effects , Endothelium, Vascular/metabolism , Lipids/blood , Male , Metabolic Syndrome/physiopathology , Nitric Oxide/blood , Nitroprusside/pharmacology , Rats , Rats, Inbred Strains , Thiobarbituric Acid Reactive Substances/analysis , Vasodilation/drug effects , Vasodilation/physiology , Vasodilator Agents/pharmacology
9.
J Pharm Pharmacol ; 58(2): 243-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16451753

ABSTRACT

We previously demonstrated that Ginkgo biloba extract (Ginkgo) produced vasodilation via the nitric oxide pathway in aortic segments isolated from Wistar rats. In this study, we have analysed the effects of daily long-term oral Ginkgo treatment on blood pressure, vascular tone, and calcium mobilization to evaluate the clinical availability. Spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY) were fed either a control diet or a diet containing 0.05%-0.5% Ginkgo for 30 days. Administration of Ginkgo did not change systolic blood pressure in WKY, but significantly decreased systolic blood pressure in SHR. In thoracic aortic preparations isolated from SHR, diminished relaxation in response to acetylcholine was improved by a Ginkgo-containing diet. This diet significantly decreased the EC50 value and significantly increased maximum relaxation in response to acetylcholine in SHR. In aortic segments isolated from WKY, acetylcholine-induced relaxation was not affected by a Ginkgo-containing diet. Sodium nitroprusside-induced relaxation was unchanged by a Ginkgo-containing diet in SHR and WKY. We also examined the effects of a Ginkgo-containing diet on the intracellular calcium level of aortic endothelium using a fluorescent confocal microscopic imaging system. Calcium Green 1/AM preloading indicated that acetylcholine significantly increased the endothelial intracellular calcium level. The Ginkgo-containing diet significantly enhanced this increase in the aortic endothelium of SHR, but did not change that of WKY. The results suggested that Ginkgo enhanced endothelium-dependent vasodilation and elevation of the endothelial intracellular Ca(2+) level in SHR, resulting in hypotension. This accelerative effect of Ginkgo on Ca(2+) mobilization seemed to be associated with restoration of impaired dilatory function induced by acetylcholine in endothelial cells.


Subject(s)
Endothelium, Vascular/drug effects , Ginkgo biloba/chemistry , Hypertension/drug therapy , Acetylcholine/pharmacology , Animals , Aorta, Thoracic/drug effects , Aorta, Thoracic/physiology , Blood Pressure/drug effects , Calcium/metabolism , Diet , Endothelium, Vascular/physiology , Hypertension/physiopathology , In Vitro Techniques , Male , Plant Extracts/therapeutic use , Rats , Rats, Inbred SHR , Rats, Wistar , Vasodilation/drug effects , Vasodilator Agents/pharmacology
10.
J Pharm Pharmacol ; 58(4): 481-7, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16597365

ABSTRACT

We demonstrated previously that stimulation of the P2Y receptor enhanced the macromolecular permeability of cultured endothelial cell monolayers via the paracellular pathway. To determine whether the P2Y receptor participates in the regulation of permeability in intact microvessels, we have examined the effects of exogenous and endogenous ATP on the permeation of the surface tissue of perfused rat tail caudal artery using a fluorescein isothiocyanate-dextran (FD-4; MW 4400; 1.0 mg mL(-1)). The permeation of FD-4 was assessed by a confocal fluorescence imaging system. We found that 2-methylthioadenosine 5'-triphosphate, a P2Y receptor agonist, enhanced the fluorescence intensity of FD-4 in the surface of the rat caudal artery tissue and that it was inhibited by pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid, a P2 receptor antagonist. Also, noradrenaline, a sympathetic neurotransmitter, and bradykinin, an inflammatory autacoid, enhanced the fluorescence intensity of FD-4 in the surface tissue of the rat caudal artery. The enhancement by noradrenaline was significantly inhibited by the P2 receptor antagonist. In addition, noradrenaline and bradykinin caused the release of ATP, ADP, AMP and adenosine from the endothelium of the rat caudal artery. These results indicated that the exogenous and endogenous ATP increased the macromolecular permeability of blood capillaries via the P2Y receptor. Such purinergic regulation of endothelial permeability may function in physiological and pathophysiological conditions.


Subject(s)
Adenosine Triphosphate/metabolism , Capillary Permeability/physiology , Adenosine Triphosphate/pharmacology , Animals , Capillary Permeability/drug effects , Male , Microcirculation/drug effects , Microcirculation/metabolism , Purinergic P2 Receptor Agonists , Rats , Rats, Wistar , Receptors, Purinergic P2/metabolism
11.
Sci Rep ; 6: 27525, 2016 06 09.
Article in English | MEDLINE | ID: mdl-27277343

ABSTRACT

Sentinel lymph node biopsy is performed as a standard procedure in breast cancer surgery, and the development of quick and simple methods to detect metastatic lesions is in high demand. Here, we validated a new fluorescent method using γ-glutamyl hydroxymethyl rhodamine green to diagnose metastatic lymph nodes in breast cancer. One hundred and forty-nine lymph nodes from 38 breast cancer patients were evaluated in this study. Comparison of fluorescent and pathological images showed that this fluorescent method was successful for visualizing breast cancer cells in lymph nodes. This method had a sufficiently high sensitivity (97%), specificity (79%) and negative predictive value (99%) to render it useful for an intraoperative diagnosis of cancer. These preliminary findings suggest that this novel method is useful for distinguishing non-cancerous specimens from those in need of careful examination and could help save time and cost for surgeons and pathologists.


Subject(s)
Breast Neoplasms/pathology , Carcinoma, Ductal, Breast/pathology , Dipeptides/chemistry , Lymphatic Metastasis/diagnostic imaging , Rhodamines/chemistry , Aged , Carcinoma, Lobular/pathology , Female , Humans , Lymph Nodes/pathology , Microscopy, Fluorescence , Middle Aged , Neoplasm Metastasis , Sensitivity and Specificity , Sentinel Lymph Node Biopsy
12.
Int J Hematol ; 82(4): 351-6, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16298830

ABSTRACT

To elucidate differences in the antigenic structure of factor VIII (FVIII) among mammals, we evaluated cross-reactivities of well-defined antihuman FVIII antibodies with canine and other mammalian FVIII proteins. Monoclonal antibodies against human FVIII recognizing the A1 domain in the heavy chain and the A3 domain in the light chain showed 2.7% and 0% cross-reactivities, respectively, with canine FVIII. The cross-reactivities of 2 alloantibodies and a monoclonal antibody that recognized the A2 domain in the heavy chain were 10%, 38%, and 0%, respectively. On the other hand, 2 kinds of alloantibodies and a monoclonal antibody recognizing the C2 domain in the light chain showed 160%, 390%, and 130% cross-reactivity, respectively, with canine FVIII. The anti-C2 monoclonal antibody (NMC-VIII/5) showed a type 2 inactivating property when tested with canine and human plasma. Moreover, cross-reactivities of NMC-VIII/5 with simian and feline FVIII were 54.5% and 82.8%, respectively, while the cross-reactivities of the anti-A2 monoclonal antibody (JR8) with simian and feline FVIII were 1.3% and 0%, respectively. These findings suggest that the antigenic structure of the C2 epitope has remained relatively conserved throughout mammalian evolution in contrast to the A2 epitope and that a canine model of hemophilia A is useful for FVIII inhibitor experiments.


Subject(s)
Factor VIII/chemistry , Animals , Antibodies, Monoclonal , Antigens/chemistry , Blood Coagulation , Conserved Sequence , Cross Reactions , Dogs , Factor VIII/immunology , Humans , Isoantibodies , Mammals , Multiprotein Complexes
13.
J Pharm Pharmacol ; 57(3): 335-40, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15807989

ABSTRACT

We have shown that P2Y receptor stimulation accelerates macromolecular permeation through the endothelial cell layer. To elucidate the mechanism of this acceleration, we examined the effects of ML-9, a myosin light chain kinase inhibitor, and Y-27632, a Rho-kinase inhibitor, on fluorescein isothiocyanate dextran (FD-4) permeation across the human umbilical vein endothelial cell monolayer. FD-4 permeation was analysed by high-performance liquid chromatography fluorescence detection. A P2Y receptor agonist, 2meS-ATP, enhanced the permeability of FD-4, which was inhibited by pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS), a P2Y-receptor antagonist. The 2meS-ATP-induced increase in the permeability of FD-4 was significantly inhibited by ML-9. Also, Y-27632 prevented the 2meS-ATP-induced increase in the permeability of FD-4. Neither ML-9 nor Y-27632 influenced the spontaneous permeation of FD-4. These results suggest that phosphorylation of the myosin light chain may play an important role in the purinergic regulation of macromolecular permeation through the vascular endothelium.


Subject(s)
Adenosine Triphosphate/analogs & derivatives , Endothelial Cells/metabolism , Endothelium, Vascular/metabolism , Fluorescein-5-isothiocyanate/analogs & derivatives , Myosin-Light-Chain Kinase/physiology , Protein Serine-Threonine Kinases/metabolism , Pyridoxal Phosphate/analogs & derivatives , Receptors, Purinergic P2/metabolism , Adenosine Triphosphate/pharmacology , Amides/pharmacology , Azepines/pharmacology , Cell Membrane Permeability , Chromatography, High Pressure Liquid , Dextrans/pharmacokinetics , Endothelium, Vascular/cytology , Fluorescein-5-isothiocyanate/pharmacokinetics , Humans , In Vitro Techniques , Intracellular Signaling Peptides and Proteins , Myosin-Light-Chain Kinase/antagonists & inhibitors , Protein Serine-Threonine Kinases/antagonists & inhibitors , Pyridines/pharmacology , Pyridoxal Phosphate/pharmacology , Thionucleotides/pharmacology , rho-Associated Kinases
15.
Case Rep Obstet Gynecol ; 2015: 424891, 2015.
Article in English | MEDLINE | ID: mdl-25954560

ABSTRACT

Uterine inversion is a state wherein the endometrial surface is inverted. Although this condition may be observed in nonpregnant women, it most commonly develops at the time of delivery. In the present case, a 37-year-old woman without any remarkable history developed acute puerperal uterine inversion after the successful induction of labor. Following the delivery, she complained twice of severe lower abdominal pain; subsequently, hemorrhage was noted at the site of partial detachment of the placenta. These findings led to a diagnosis of placenta accreta, and the patient developed a state of shock. A Bakri postpartum balloon was inserted into the uterine cavity under ultrasonographic guidance and was filled with physiological saline for treatment of this condition. With this procedure, the uterine inversion was completely reduced and the hemorrhage was stopped. Moreover, no reinversion was observed in the postoperative period. These findings suggest that a Bakri postpartum balloon can be used to noninvasively reduce uterine inversion and prevent its recurrence.

16.
Sci Rep ; 5: 12080, 2015 Jul 13.
Article in English | MEDLINE | ID: mdl-26165706

ABSTRACT

We previously developed γ-glutamyl hydroxymethyl rhodamine green (gGlu-HMRG) as a tool to detect viable cancer cells, based on the fact that the enzyme γ-glutamyltranspeptidase (GGT) is overexpressed on membranes of various cancer cells, but is not expressed in normal tissue. Cleavage of the probe by GGT generates green fluorescence. Here, we examined the feasibility of clinical application of gGlu-HMRG during breast-conserving surgery. We found that fluorescence derived from cleavage of gGlu-HMRG allowed easy discrimination of breast tumors, even those smaller than 1 mm in size, from normal mammary gland tissues, with 92% sensitivity and 94% specificity, within only 5 min after application. We believe this rapid, low-cost method represents a breakthrough in intraoperative margin assessment during breast-conserving surgery.


Subject(s)
Breast Neoplasms/diagnosis , Breast Neoplasms/pathology , Breast/pathology , Fluorescent Dyes/metabolism , Rhodamines/metabolism , gamma-Glutamyltransferase/metabolism , Breast/metabolism , Breast Neoplasms/metabolism , Cell Line, Tumor , Female , Humans , MCF-7 Cells , Sensitivity and Specificity
17.
Life Sci ; 75(9): 1113-22, 2004 Jul 16.
Article in English | MEDLINE | ID: mdl-15207658

ABSTRACT

We examined hepatic cytochrome P450 (CYP)-mediated interactions between Ginkgo biloba extract (GBE) and tolbutamide, an oral anti-diabetic agent, in aged and young rats. Tolbutamide was orally given to rats with or without GBE treatment, and time-dependent changes in blood glucose were monitored. The basal activity of six CYP subtypes in liver was lower in the aged rats than in the young rats, while the inductions of these enzymes by 5 day pretreatment of 0.1% GBE diet were more in the aged rats. Further, the pretreatment of GBE significantly attenuated the hypoglycemic action of tolbutamide in the aged rats, corresponding well to the enhanced activity of (S)-warfarin 7-hydroxylase, which is responsible for CYP2C9 subtype, a major isoform metabolizing tolbutamide. In contrast, the simultaneous administration of GBE with tolbutamide potentiated the hypoglycemic action of this drug. The in vitro experiments revealed that GBE competitively inhibited the metabolism of tolbutamide by (S)-warfarin 7-hydroxylase in the rat liver microsomes. In the young rats, the 5 day pretreatment with GBE significantly attenuated the hypoglycemic action of tolbutamide, but a simultaneous treatment had little influence on the tolbutamide effect. In conclusion, the present study has shown that the simultaneous and continuous intake of GBE significantly affects the hypoglycemic action of tolbutamide, possibly via a hepatic CYP enzyme-mediated mechanism, particularly in the aged rats. Therefore, it is anticipated that the intake of GBE as a dietary supplement with therapeutic drugs should be cautious, particularly in elderly people.


Subject(s)
Cytochrome P-450 Enzyme System/metabolism , Ginkgo biloba/chemistry , Liver/drug effects , Plant Extracts/pharmacology , Tolbutamide/metabolism , Analysis of Variance , Animals , Aryl Hydrocarbon Hydroxylases/metabolism , Blood Glucose/drug effects , Blood Glucose/metabolism , Chromatography, High Pressure Liquid , Cytochrome P-450 CYP2C9 , Drug Interactions , Liver/enzymology , Male , Microsomes, Liver/metabolism , Rats , Rats, Wistar
18.
Life Sci ; 70(23): 2783-92, 2002 Apr 26.
Article in English | MEDLINE | ID: mdl-12269382

ABSTRACT

Ginkgo biloba extract (GBE) has been used clinically for improving peripheral vascular diseases in France and Germany and is ingested widely as a herbal medicine in some countries. However, accurate information about its safety as an herbal medicine has not been sufficiently established. To address this issue, we examined the effect of GBE on hepatic drug metabolizing enzymes and their influence on hypotensive drug in rats. Male rats were fed either a control diet or diet containing GBE (0.5% w/w) for 4 weeks. The feeding of a GBE diet did not change the serum transaminase activity, but increased the liver weight and the phospholipid concentration in the liver. In addition, the GBE diet markedly increased the content of cytochrome P-450 (CYP), and the activity of glutathione S-transferase in the liver. Furthermore, the GBE diet markedly induced levels of CYP2B1/2, CYP3A1 and CYP3A2 mRNA in the liver. The levels of CYP1A1, CYP1A2, CYP2E1, CYP2C11 and CYP4A1 were unchanged. The feeding of GBE for 4 weeks significantly reduced the hypotensive effect of nicardipine that was reported to be metabolized by CYP3A2 in rats. These findings suggest that GBE reduces the therapeutic potency of the Ca2+ channel blocker, nicardipine, via enhancement of cytochrome P-450 expression.


Subject(s)
Calcium Channel Blockers/therapeutic use , Cytochrome P-450 Enzyme System/genetics , Gene Expression/drug effects , Hypotension/prevention & control , Liver/drug effects , Nicardipine/therapeutic use , Plant Extracts/administration & dosage , Animals , Calcium/metabolism , Cells, Cultured , Cytochrome P-450 Enzyme System/metabolism , Diet , Dose-Response Relationship, Drug , Drug Interactions , Ginkgo biloba , Glutathione Transferase/metabolism , Hypotension/enzymology , Isoenzymes/metabolism , Liver/enzymology , Male , RNA, Messenger/metabolism , Rats , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction
19.
Life Sci ; 72(13): 1445-53, 2003 Feb 14.
Article in English | MEDLINE | ID: mdl-12535713

ABSTRACT

The effects of P2 receptor agonists on cell size and intracellular calcium levels, [Ca(2+)](i), was investigated using cultured endothelial cells isolated from the caudal artery of male Wistar rats. Cell size and [Ca(2+)](i) were measured using a phase-contrast and fluorescent confocal microscopic image analyzer and a Calcium Green fluorescence probe. P2Y receptor agonists, 2-methylthio ATP (2meS-ATP), ADP, UTP and ATP decreased the cell size and increased [Ca(2+)](i) in endothelial cells from rat caudal artery. However, alpha,beta-methylene ATP, a P2X receptor agonist, did not induce these responses. The decrease in size and the increase in [Ca(2+)](i), by 2meS-ATP were blocked by PPADS (P2-antagonist), suramin (P2-antagonist), thapsigargin (Ca(2+) pump inhibitor) and U-73122 (phospholipase C inhibitor). The present results show that activation of P2Y receptors, not P2X receptors, induces a decrease in cell size and an increase in [Ca(2+)](i), and the pharmacological properties of these two responses are the same. We concluded that the size of endothelial cells is regulated by P2Y receptors via intracelluar Ca(2+) derived from Ca(2+) stores.


Subject(s)
Adenosine Triphosphate/analogs & derivatives , Calcium/metabolism , Cell Size/drug effects , Endothelium, Vascular/cytology , Pyridoxal Phosphate/analogs & derivatives , Receptors, Purinergic P2/physiology , Adenosine Triphosphate/metabolism , Adenosine Triphosphate/pharmacology , Animals , Endothelium, Vascular/drug effects , Endothelium, Vascular/metabolism , Enzyme Inhibitors/pharmacology , Estrenes/pharmacology , Male , Osmotic Pressure , Phosphodiesterase Inhibitors/pharmacology , Purinergic P2 Receptor Agonists , Pyridoxal Phosphate/pharmacology , Pyrrolidinones/pharmacology , Rats , Rats, Wistar , Receptors, Purinergic P2/drug effects , Suramin/pharmacology , Thapsigargin/pharmacology , Thionucleotides/pharmacology
20.
Clin Exp Pharmacol Physiol ; 31 Suppl 2: S29-30, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15649281

ABSTRACT

1. Changes in the cardiovascular parameters of Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR) were examined following a 4-week diet of either Brazilian propolis or Eucommia uloides OLIVER (tochu). 2. A 4-week diet of propolis or tochu resulted in significant reductions in systolic blood pressure in SHR but had no effect on WKY. Experiments using aorta isolated from animals fed a diet of propolis or tochu revealed increased acetylcholine-induced relaxation in SHR and no change in acetylcholine-induced relaxation in WKY. Sodium nitroprusside-induced relaxation was unaffected by propolis or tochu in both animal groups. 3. These results suggest that propolis and tochu produce an antihypertensive effect that may be mediated by potentiation of acetylcholine-induced vasodilatation.


Subject(s)
Antihypertensive Agents/therapeutic use , Eucommiaceae , Hypertension/drug therapy , Propolis , Animals , Aorta, Thoracic/drug effects , Aorta, Thoracic/physiology , Brazil , Hypertension/physiopathology , Male , Rats , Rats, Inbred SHR , Rats, Inbred WKY , Vasodilation/drug effects , Vasodilation/physiology
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