1.Effects of Ambient Changes on ADLs of Patients As Assessed by Use of Barthel Index--In the Cases of Stroke and Femoral Neck Fracture Patients--
Taizo YAMAMOTO ; Hiroko WATANABE ; Yoshimichi HIDANO ; Shuzo SHINTANI ; Taro HINO ; Jun AKANUMA ; Masayoshi MASUYAMA
Journal of the Japanese Association of Rural Medicine 2010;59(2):67-71
When subacute elderly patients are transferred from an acute hospital to a rehabilitation facility, the likelihood is that the environmental change will decrease the patients' ability to perform the basic activities of daily living (ADLs). In this study, we assessed the effects of the ambient changes on ADLs by the use of the Barthel Index, the reliability as well as validity of which is rated high for assessing the patient's fundamental ability. Our subjects consisted of the patients with hemiplegia who had undergone medical treatment of stroke and those who had been operated on for femoral neck fracture (FNF) in Toride Kyodo General Hospital. They were transferred to the convalescent rehabilitation ward (CRW) of Aida Memorial Rehabilitation Hospital, affiliated with our hospital. We compared the BI scores given to the patients by physical, occupational and speech therapists, when discharged from our hospital, and those scores given by nurses within one week after the patients moved to the CRW. Differences between BI scores given at Toride Hospital and those at the rehabilitation hospital averaged -5.9±16.0 points for stroke patients and -7.3±14.1 pointsfor FNF patients. Spearman's rank correlation coefficient of BI scores in the acute hospital and in the CRW for stroke patients was 0.91 (p<0.001) and 0.69 (p<0.001) for FNF. There was no significant difference in changes in BI scores between stroke and FNF. However, there was a tendency for the patients' functional ability in daily living to be assessed lower in the FNF patients than in the stroke patients. This was probably because the former were older than the latter on the average. The average age of the FNF patients was 81.4 years and that of the stroke patients was 68.5 years.
2.Role of gap junctions in the endothelium-dependent hyperpolarization of vascular smooth muscle cells.
Yoshimichi YAMAMOTO ; Megan F KLEMM ; Hikaru HASHITANI ; J Richard LANG ; Tsuyoshi SOJI ; Hikaru SUZUKI
The Korean Journal of Physiology and Pharmacology 2001;5(1):1-8
Hyperpolarization of arterial smooth muscle by acetylcholine is considered to be produced by the release of an unidentified chemical substance, an endothelium-derived hyperpolarizing factor (EDHF). Several chemicals have been proposed as the candidate for EDHF. However, none of them fulfil completely the nature and property of EDHF. Ultrastructural observation with electron microscope reveals that in some arteries, gap junctions are formed between endothelial and smooth muscle cells. In small arterioles, injection of gap junction permeable dyes into an endothelial cell results in a distribution of the dye to surrounding cells including smooth muscle cells. These observations allow the speculation that myoendothelial gap junctions may have a functional significance. Simultaneous measurement of the electrical responses in both endothelial and smooth muscle cells using the double patch clamp method demonstrates that these two cell types are indeed electrically coupled, indicating that they behave as a functional syncytium. The EDHF-induced hyperpolarization is produced by an activation of Ca2+-sensitive K+-channels that are inhibited by charybdotoxin and apamin. Agonists that release EDHF increase (Ca2+)i in endothelial cells but not in smooth muscle cells. Inhibition of gap junctions with chemical agents abolishes the agonist-induced hyperpolarization in smooth muscle cells but not in endothelial cells. All these observations can be explained if EDHF is an electrotonic signal propagating from endothelium to smooth muscle cells through gap junctions.
Acetylcholine
;
Apamin
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Arteries
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Arterioles
;
Calcium
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Charybdotoxin
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Coloring Agents
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Endothelial Cells
;
Endothelium
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Gap Junctions*
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Giant Cells
;
Muscle, Smooth
;
Muscle, Smooth, Vascular*
;
Myocytes, Smooth Muscle
;
Potassium Channels