Blood Viscosity and Cerebral Blood Flow

It is well known that there is a close correlation between blood viscosity and blood flow. To clarify any relationship between blood viscosity and regional cerebral blood flow (rCBF) in the elderly, we simultaneously studied both CBF with PET (positron emission tomography) and blood viscosity with v...

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Published inNihon Rōnen Igakkai zasshi Vol. 30; no. 3; pp. 174 - 181
Main Authors Shirakura, Takuo, Tamura, Kousei, Kubota, Kazuo
Format Journal Article
LanguageJapanese
Published The Japan Geriatrics Society 1993
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ISSN0300-9173
DOI10.3143/geriatrics.30.174

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Abstract It is well known that there is a close correlation between blood viscosity and blood flow. To clarify any relationship between blood viscosity and regional cerebral blood flow (rCBF) in the elderly, we simultaneously studied both CBF with PET (positron emission tomography) and blood viscosity with viscosimeter before and after phlebotomy in the elderly with various kinds of polycythemia. These subjects consisted of five male cases of secondary polycythemia due to pulmonary fibrosis, one male case of essential erythrocytosis (average age 66.6±4.6 years old) and one female case of stress polycythemia (47 years old). Before phlebotomy an increase in blood viscosity, decrease in rCBF and regional cerebral matablic rate of oxygen (rCMRO2) were observed in all cases. After phlebotomy (total amount of 800 to 1, 000ml) blood viscosity rapidly decreased, and both rCBF and rCMRO2 tended to increase. There was a significant negative or positive correlation between CBF and blood viscosity or rCMRO2, respectively. However, no increase in cerebral oxygen transport was observed in any subject after phlebotomy. It was noted that cerebral infarction is not infrequent among elderly visitors to Kusatsu spa, which is characterized by high temperature hot spring water. From the authors' observation of 23 cases of cerebral infarction encountered during the last five years, it is noteworthy that the disease tended to occur more frequently during midnight to morning, specially 3:00 to 6:00. Thus, to clarify the pathogenetic mechanism of the cerebral infarction occurring after bathing in hot spring water, we studied the changes in blood viscosity, blood pressure and coagulation-fibrinolytic system after bathing in hot spring water. The results obtained were as follows. After bathing in hot spring water (42-47°C for 3 to 10min, at 16:00), a significant elevation of blood viscosity was observed from 4:00 to 8:00 and a significant lowering of blood pressure from 20:00 to 8:00 compared with bathing in plain water. In addition, bathing in high temperature water resulted in a decrease in tPA (tissue-typed plasminogen activator) and an increase in PAI-1 (plasminogen activator inhibitor-1). An in vitro study using human umbilical vein endothelial cell (HUVEC) revealed that a high temperature during incubation stimulates secretion of PAT-1 into the blood stream from vascular endothelial cells. From these results it is speculated that hemoconcentration, vasodilatation and inhibition of the fibrinolytic system caused due to the thermal insulation effect of hot spring water might play some role in the pathogenetic mechanism of cerebral infarction, which tends to occur from midnight to the early morning in the elderly visitors.
AbstractList It is well known that there is a close correlation between blood viscosity and blood flow. To clarify any relationship between blood viscosity and regional cerebral blood flow (rCBF) in the elderly, we simultaneously studied both CBF with PET (positron emission tomography) and blood viscosity with viscosimeter before and after phlebotomy in the elderly with various kinds of polycythemia. These subjects consisted of five male cases of secondary polycythemia due to pulmonary fibrosis, one male case of essential erythrocytosis (average age 66.6±4.6 years old) and one female case of stress polycythemia (47 years old). Before phlebotomy an increase in blood viscosity, decrease in rCBF and regional cerebral matablic rate of oxygen (rCMRO2) were observed in all cases. After phlebotomy (total amount of 800 to 1, 000ml) blood viscosity rapidly decreased, and both rCBF and rCMRO2 tended to increase. There was a significant negative or positive correlation between CBF and blood viscosity or rCMRO2, respectively. However, no increase in cerebral oxygen transport was observed in any subject after phlebotomy. It was noted that cerebral infarction is not infrequent among elderly visitors to Kusatsu spa, which is characterized by high temperature hot spring water. From the authors' observation of 23 cases of cerebral infarction encountered during the last five years, it is noteworthy that the disease tended to occur more frequently during midnight to morning, specially 3:00 to 6:00. Thus, to clarify the pathogenetic mechanism of the cerebral infarction occurring after bathing in hot spring water, we studied the changes in blood viscosity, blood pressure and coagulation-fibrinolytic system after bathing in hot spring water. The results obtained were as follows. After bathing in hot spring water (42-47°C for 3 to 10min, at 16:00), a significant elevation of blood viscosity was observed from 4:00 to 8:00 and a significant lowering of blood pressure from 20:00 to 8:00 compared with bathing in plain water. In addition, bathing in high temperature water resulted in a decrease in tPA (tissue-typed plasminogen activator) and an increase in PAI-1 (plasminogen activator inhibitor-1). An in vitro study using human umbilical vein endothelial cell (HUVEC) revealed that a high temperature during incubation stimulates secretion of PAT-1 into the blood stream from vascular endothelial cells. From these results it is speculated that hemoconcentration, vasodilatation and inhibition of the fibrinolytic system caused due to the thermal insulation effect of hot spring water might play some role in the pathogenetic mechanism of cerebral infarction, which tends to occur from midnight to the early morning in the elderly visitors.
Author Kubota, Kazuo
Tamura, Kousei
Shirakura, Takuo
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References 6) Brown MM, Marshall J: Effect of plasma exchange on blood viscosity and cerebral blood flow. Brit Med J 1982; 284: 1733-1736.
8) Brown MM, Wade JPH, Marshall J: Fundamental importance of arterial oxygen content in the regulation of cerebral blood flow in man. Brain 1985; 108: 81-93.
4) Thomas DJ, du Boulay GH, Marshall J, Pearson TC, Russell RRW, Symon L, Wetherley- Mein G, Zilkha E: Cerebral blood-flow in polycythaemia. Lancet 1977; ii: 161-163.
5) Thomas DJ, Zilkha E, Redmond S, du Boulay GH, Marshall J, J, Russell RRW, Symon L, Wetherley-Mein G, Zilkha E; Effect of haematocrit on cerebral blood-flow in man. Lancet 1977; ii: 941-943.
14) 久保田一雄, 柳沢勉, 倉林均, 田村遵一, 白倉卓夫: 血液粘度の日内変動からみた脳梗塞及び心筋梗塞の発症機序に関する検討. 第1報. 若年男性における飲酒及び温泉浴の血液粘度の日内変動に及ぼす影響. 日温気物医誌1990; 53: 137-140.
9) Agnoli A, Manfredi M, Mossuto L, Piccinelli A: Rapport entre les rythmes hemeronyctaux de la tension arterielle et sa pathogenie de l' insuffisance vasculaire cerebrale. Rev Neurol 1975; 131: 597-606.
11) Miller-Craig MW, Bishop CN, Raftery EB: Circadian variation of blood pressure. Lancet 1978; i: 795-797.
10) Marshall J: Diurnal vaiation in occurrence of stroke. Stroke 1977; 8: 230-231.
16) Kurabayashi H, Kubota K, Tamura J, Shirakura T; A glass of water at midnight for possible prevention of cerebral infarction. Stroke 1991; 22: 1326-1327.
15) 白倉卓夫, 菅井芳郎: 草津温泉, 高温泉浴 (時間湯) の血小板機能におよぼす影響. 日生気誌1984; 21; 18.
3) Nelson D, Fazekas JF: Cerebral blood flow in polycythemia vera. Arch Intern Med 1956; 98: 328-331.
13) Kubota K, Sakurai T, Tamura J, Shirakura T: Is the circadian change in hematocrit and blood viscosity a factor triggering cerebral and myocardial infarction? Stroke 1987; 18: 812-813.
2) Kety SS: The physiology of the human cerebral circulation. Anesthesiology 1949; 10: 610-614.
12) Turton MB, Deegan T: Circadian variations of plasma cathecholamine, cortisol and immunoreactive insulin concentrations in supine subjects. Clin Chim Acta 1974; 55: 389-397.
7) Brown MM: The influence of pathological and therapeutic changes in blood viscosity on cerebral blood flow in man. MD Thesis, Cambridge, 1984.
1) 白倉卓夫, 高橋龍太郎, 村井善郎, 村上元孝, 松田保, 菅井芳郎: 老年者 stress erythrocytosis の血液学的検討. 日老医誌1979; 6: 528-535.
References_xml – reference: 14) 久保田一雄, 柳沢勉, 倉林均, 田村遵一, 白倉卓夫: 血液粘度の日内変動からみた脳梗塞及び心筋梗塞の発症機序に関する検討. 第1報. 若年男性における飲酒及び温泉浴の血液粘度の日内変動に及ぼす影響. 日温気物医誌1990; 53: 137-140.
– reference: 2) Kety SS: The physiology of the human cerebral circulation. Anesthesiology 1949; 10: 610-614.
– reference: 16) Kurabayashi H, Kubota K, Tamura J, Shirakura T; A glass of water at midnight for possible prevention of cerebral infarction. Stroke 1991; 22: 1326-1327.
– reference: 12) Turton MB, Deegan T: Circadian variations of plasma cathecholamine, cortisol and immunoreactive insulin concentrations in supine subjects. Clin Chim Acta 1974; 55: 389-397.
– reference: 8) Brown MM, Wade JPH, Marshall J: Fundamental importance of arterial oxygen content in the regulation of cerebral blood flow in man. Brain 1985; 108: 81-93.
– reference: 11) Miller-Craig MW, Bishop CN, Raftery EB: Circadian variation of blood pressure. Lancet 1978; i: 795-797.
– reference: 13) Kubota K, Sakurai T, Tamura J, Shirakura T: Is the circadian change in hematocrit and blood viscosity a factor triggering cerebral and myocardial infarction? Stroke 1987; 18: 812-813.
– reference: 10) Marshall J: Diurnal vaiation in occurrence of stroke. Stroke 1977; 8: 230-231.
– reference: 7) Brown MM: The influence of pathological and therapeutic changes in blood viscosity on cerebral blood flow in man. MD Thesis, Cambridge, 1984.
– reference: 5) Thomas DJ, Zilkha E, Redmond S, du Boulay GH, Marshall J, J, Russell RRW, Symon L, Wetherley-Mein G, Zilkha E; Effect of haematocrit on cerebral blood-flow in man. Lancet 1977; ii: 941-943.
– reference: 6) Brown MM, Marshall J: Effect of plasma exchange on blood viscosity and cerebral blood flow. Brit Med J 1982; 284: 1733-1736.
– reference: 9) Agnoli A, Manfredi M, Mossuto L, Piccinelli A: Rapport entre les rythmes hemeronyctaux de la tension arterielle et sa pathogenie de l' insuffisance vasculaire cerebrale. Rev Neurol 1975; 131: 597-606.
– reference: 1) 白倉卓夫, 高橋龍太郎, 村井善郎, 村上元孝, 松田保, 菅井芳郎: 老年者 stress erythrocytosis の血液学的検討. 日老医誌1979; 6: 528-535.
– reference: 15) 白倉卓夫, 菅井芳郎: 草津温泉, 高温泉浴 (時間湯) の血小板機能におよぼす影響. 日生気誌1984; 21; 18.
– reference: 3) Nelson D, Fazekas JF: Cerebral blood flow in polycythemia vera. Arch Intern Med 1956; 98: 328-331.
– reference: 4) Thomas DJ, du Boulay GH, Marshall J, Pearson TC, Russell RRW, Symon L, Wetherley- Mein G, Zilkha E: Cerebral blood-flow in polycythaemia. Lancet 1977; ii: 161-163.
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Snippet It is well known that there is a close correlation between blood viscosity and blood flow. To clarify any relationship between blood viscosity and regional...
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StartPage 174
SubjectTerms Blood viscosity
CBF
CMRO2
Fibrinolytic system
Hyperthermia
Title Blood Viscosity and Cerebral Blood Flow
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