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1.
Appl Radiat Isot ; 78: 82-7, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23685725

ABSTRACT

In the present study, the influences of particulate matter (PM) and seasonal monsoons on (7)Be concentrations in surface air (CBe) are elucidated. The (7)Be and the corresponding PM concentrations in the air were monitored simultaneously throughout a 14-year period (1998-2011) in Hsinchu, Taiwan. During the autumn and winter seasons (Oct.-Feb.), both the PM and the (7)Be concentrations increased as a result of the northeasterly monsoon. In contrast, the lowest PM and (7)Be concentrations were observed in July and August. This timing is due to the occurrence of southwest monsoons, which carry air masses with low PM concentrations and are associated with depleted (7)Be from low latitudes. The activity concentration of (7)Be in the PM (APM) was used to explain the seasonal variations of (7)Be with respect to the PM concentrations. In contrast, APM is not sensitive enough to vary with the seasons. The air masses transported by the monsoons are believed to be partially mixed with the PM locally produced in Taiwan, which explains their seasonal variations. The (7)Be concentrations in surface air can be experimentally predicted from the PM concentrations based on CBe (mBq/m(3))=0.0767 PM (µg/m(3)) across seasons. The annual averages of the PM and (7)Be concentrations are 48.1 µg/m(3) and 3.7 mBq/m(3), respectively. The estimated CBe was either slightly overestimated or underestimated, depending on the season. The highest deviations occurred in July and August, when CBe was underestimated by 33%.


Subject(s)
Air Pollution, Radioactive/statistics & numerical data , Atmosphere/chemistry , Beryllium/analysis , Particulate Matter/analysis , Radiation Monitoring/statistics & numerical data , Radioisotopes/analysis , Weather , Air Pollution, Radioactive/analysis , Radiation Dosage , Seasons , Taiwan
2.
Appl Radiat Isot ; 70(2): 415-22, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22056921

ABSTRACT

In the present study, factors that influence the distribution and variation of (7)Be in Hsinchu, Taiwan were elucidated. The (7)Be activity including the deposition flux and air concentration was continuously monitored and recorded throughout a 15-year period (1996-2010). To explain the observed variability in the (7)Be activity over time, air concentration and deposition flux of (7)Be were correlated to rainfall and solar activity. The monthly average deposition flux and air concentration of (7)Be were inversely related to solar activity with the 11-year cycle and were not strongly correlated to rainfall. The highest seasonal deposition flux of (7)Be occurred in March, which is commonly referred to as the spring maximum, due to air-mass mixing processes in the troposphere. The air concentration of (7)Be was seasonally variable and was significantly affected by monsoons. The lowest deposition flux and air concentration of (7)Be were observed in July and August due to the occurrence of southwest monsoons from low latitudes, which carry air masses with low concentrations of (7)Be. The deposition flux was enhanced by precipitation, which increased the deposition velocity, transferring more (7)Be from the troposphere to the ground. The fraction of dry to total deposition varied seasonally and was equal to 9.86%, on average.

3.
Clin Exp Hypertens ; 21(7): 1111-27, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10513831

ABSTRACT

Nitric oxide (NO) has been implicated in the control of renin secretion in experimental animals but little information is available concerning its role in humans. The aim of the present study was to investigate the effects of inhibition of NO synthesis on resting renin secretion and on the renin secretory responses to activation of the macula densa and sympathetic neural mechanisms controlling renin secretion. In eight healthy subjects, injection of furosemide increased plasma renin activity (PRA) with little or no change in blood pressure or heart rate. Injection of the NO synthase inhibitor L-NMMA increased blood pressure and decreased heart rate and PRA, but failed to alter the PRA response to furosemide. In another ten subjects, standing increased PRA. L-NMMA again decreased PRA but failed to alter the PRA response to standing. These results suggest that NO participates in the regulation of resting renin secretion in humans, and provide preliminary evidence that NO does not contribute significantly to the renin responses to activation of the macula densa or sympathetic mechanisms controlling renin secretion.


Subject(s)
Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide/physiology , Renin/metabolism , Adolescent , Adult , Blood Pressure/drug effects , Diuretics/pharmacology , Enzyme Inhibitors/pharmacology , Exercise/physiology , Female , Furosemide/pharmacology , Heart Rate/drug effects , Humans , Infusions, Intravenous , Male , Radioimmunoassay , Reference Values , Renin/blood , Supine Position/physiology , omega-N-Methylarginine/pharmacology
4.
J Pharmacol Exp Ther ; 290(1): 16-9, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10381754

ABSTRACT

One of the major signaling molecules involved in the regulation of renin secretion is cyclic AMP (cAMP). The concentration of cAMP in cells is determined in part by the rate of cAMP hydrolysis by several families of phosphodiesterases, especially the phosphodiesterase III family, but little is known about the roles of these enzymes in the control of renin secretion, particularly in humans. The aim of the present study was to investigate the effect of the phosphodiesterase III inhibitor milrinone on renin secretion in human subjects. Milrinone was infused i.v. in eight healthy normotensive subjects in a dose of 100 microgram/kg. Immediately after the infusion, there was a transient increase in systolic pressure from 107 +/- 5 to 116 +/- 5 mm Hg (p <.01), but no significant change in diastolic or mean arterial pressure. Heart rate increased from 67 +/- 2 to 86 +/- 4 beats/min (p <.01) and remained elevated. Plasma renin activity increased in all subjects, the mean value increasing from 3.0 +/- 0.5 to 6.0 +/- 1.1 ng/ml/h at 15 min (p <.01). These results demonstrate that milrinone increases renin secretion in human subjects, thus providing evidence that phosphodiesterase III family participates in the control of renin secretion in humans. The increase in renin secretion does not appear to be mediated by major mechanisms that control renin secretion, and likely results from an increase in cAMP concentration in the juxtaglomerular cells.


Subject(s)
3',5'-Cyclic-AMP Phosphodiesterases/antagonists & inhibitors , Milrinone/pharmacology , Phosphodiesterase Inhibitors/pharmacology , Renin/blood , Adult , Blood Pressure/drug effects , Cyclic AMP/biosynthesis , Cyclic Nucleotide Phosphodiesterases, Type 3 , Diet, Sodium-Restricted , Female , Heart Rate/drug effects , Humans , Male , Middle Aged , Renin/metabolism , Sodium/blood
5.
Clin Exp Hypertens ; 19(7): 1047-63, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9310203

ABSTRACT

It has been reported that acupuncture can decrease blood pressure in patients with hypertension, possibly by an endocrine mechanism. The aim of the present study was to investigate the effects of acupuncture on arterial blood pressure and the secretion of renin, vasopressin and cortisol in hypertensive patients. Acupuncture was performed in fifty untreated essential hypertensive patients resting in the supine position. Thirty min after acupuncture there were decreases in systolic pressure from 169 +/- 2 to 151 +/- 2 mm Hg, diastolic pressure from 107 +/- 1 to 96 +/- 1 mm Hg, and heart rate from 77 +/- 2 to 72 +/- 2 bpm (P < 0.01). Plasma renin activity decreased from 1.7 +/- 0.4 to 1.1 +/- 0.2 ng/ml/2h (P < 0.01), but there were no significant changes in plasma vasopressin or cortisol concentrations. These results confirm that acupuncture decreases blood pressure in hypertensive patients, and suggest that the decrease results, at least in part, from a decrease in renin secretion.


Subject(s)
Acupuncture Therapy , Blood Pressure/physiology , Hypertension/physiopathology , Adolescent , Adult , Female , Heart Rate , Humans , Hydrocortisone/blood , Hypertension/blood , Hypertension/therapy , Male , Middle Aged , Radioimmunoassay , Renin/blood , Supine Position , Vasopressins/blood
6.
Fundam Clin Pharmacol ; 9(4): 309-23, 1995.
Article in English | MEDLINE | ID: mdl-8566930

ABSTRACT

Research during recent years has established nitric oxide as a unique signaling molecule that plays important roles in the regulation of the cardiovascular, nervous, renal, immune and other systems. Nitric oxide has also been implicated in the control of the secretion of hormones by the pancreas, hypothalamus, pituitary and other endocrine glands, and evidence is accumulating that it contributes to the regulation of the secretion of renin by the kidneys. The enzyme nitric oxide synthetase is present in vascular and tubular elements of the kidney, particularly in cells of the macula densa, a structure that plays an important role in the control of renin secretion. Guanylyl cyclase, a major target for nitric oxide, is also present in the kidney and is responsive to changes in nitric oxide levels. Drugs that inhibit nitric oxide synthesis generally suppress renin release in vivo and in vitro, suggesting a stimulatory role for the L-arginine-nitric oxide pathway in the control of renin secretion. Under some conditions, however, blockade of nitric oxide synthesis increases renin secretion. Recent studies indicate that nitric oxide not only contributes to the regulation of basal renin secretion, but also participates in the renin secretory responses to activation of the renal baroreceptor, macula densa and beta adrenoceptor mechanisms that regulate renin secretion. Future research should clarify the mechanisms by which nitric oxide regulates the secretion of renin and establish the physiological significance of this regulation.


Subject(s)
Kidney/metabolism , Nitric Oxide/physiology , Renin/metabolism , Animals , Arginine/metabolism , Guanylate Cyclase/metabolism , Kidney/blood supply , Kidney/enzymology , Kidney Tubules, Distal/cytology , Kidney Tubules, Distal/enzymology , Kidney Tubules, Distal/metabolism , Nitric Oxide/metabolism , Nitric Oxide Synthase/antagonists & inhibitors , Nitric Oxide Synthase/metabolism , Pressoreceptors/drug effects , Pressoreceptors/metabolism , Receptors, Adrenergic, beta/drug effects , Receptors, Adrenergic, beta/metabolism
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