The effect of an adrenaline infusion on the splenic blood flow and intrasplenic platelet kinetics

2008 ◽  
Vol 67 (2) ◽  
pp. 187-192
Author(s):  
Hans Wadenvik ◽  
Jack Kutti
1987 ◽  
Author(s):  
H Wadenvik ◽  
I Denfors ◽  
J Kutti

It is well recognized that adrenaline decreases and isoprenaline increases the splenic pooling of platelets. However, the action of these adrenergic drugs on the splenic pooling mechanism is still unclear. The aim of the present study was to investigate the effect of an adrenaline and an isoprenaline infusion on intrasplenic platelet kinetics.Methods. 13 healthy male volunteers were recruited for the study. Autologous platelets were labelled with 111-Indium-oxine. 6 of the subjects received an isoprenaline infusion (0.03 ug/kg/min) over 30 min, 4 an adrenaline infusion (0.2 ug/kg/min) and 3 an adrenaline infusion (0.1 ug/kg/min) over 40 min. The splenic blood flow (SBF), intrasplenic platelet transit time (PTT) and splenic platelet pool size (SPP) were determined twice by compartmental analysis of the equilibration of radiolabelled platelets between circulating blood and splenic platelet pool: at baseline and during the infusions. The initial distribution of injected radiolabelled platelets, between blood and splenic platelet pool, was followed dynamically with a computer assisted gamma camera. Student’s t-test for paired data was employed for comparison of mean values.Comments. The adrenaline infusion diminished the exchangeable splenic platelet pool size by lowering the splenic blood flow. In contrast, the isoprenaline infusion increased the splenic pooling of platelets by increasing the splenic blood flow.


1995 ◽  
Vol 79 (3) ◽  
pp. 1008-1026 ◽  
Author(s):  
D. R. Fine ◽  
D. Glasser ◽  
D. Hildebrandt ◽  
J. Esser ◽  
R. E. Lurie ◽  
...  

Hepatic function can be characterized by the activity/time curves obtained by imaging the aorta, spleen, and liver. Nonparametric deconvolution of the activity/time curves is clinically useful as a diagnostic tool in determining organ transit times and flow fractions. The use of this technique is limited, however, because of numerical and noise problems in performing deconvolution. Furthermore, the interaction of part of the tracer with the spleen and gastrointestinal tract, before it enters the liver, further obscures physiological information in the deconvolved liver curve. In this paper, a mathematical relationship is derived relating the liver activity/time curve to portal and hepatic behavior. The mathematical relationship is derived by using transit time spectrum/residence time density theory. Based on this theory, it is shown that the deconvolution of liver activity/time curves gives rise to a complex combination of splenic, gastrointestinal, and liver dependencies. An anatomically and physiologically plausible parametric model of the hepatic vascular system has been developed. This model is used in conjunction with experimental data to estimate portal, splenic, and hepatic physiological blood flow parameters for eight normal volunteers. These calculated parameters, which include the portal flow fraction, the splenic blood flow fraction, and blood transit times are shown to adequately correspond to published values. In particular, the model of the hepatic vascular system identifies the portal flow fraction as 0.752 +/- 0.022, the splenic blood flow fraction as 0.180 +/- 0.023, and the liver mean transit time as 13.4 +/- 1.71 s. The model has also been applied to two portal hypertensive patients. The variation in some of the model parameters is beyond normal limits and is consistent with the observed pathology.


1969 ◽  
Vol 98 (1) ◽  
pp. 65-74 ◽  
Author(s):  
Toshio Sato ◽  
Kenji Koyama ◽  
Kenichi Watanabe ◽  
Shunichi Kimura

2018 ◽  
Vol 96 (11) ◽  
pp. 1060-1068
Author(s):  
Sara A. Ruggiero ◽  
Jason S. Huber ◽  
Coral L. Murrant ◽  
Keith R. Brunt ◽  
Jeremy A. Simpson

2002 ◽  
Vol 34 ◽  
pp. A45
Author(s):  
F. Patrizi ◽  
A. De Santis ◽  
L. Miglioresi ◽  
P. Saccenti ◽  
T. Marinelli ◽  
...  
Keyword(s):  

2008 ◽  
Vol 67 (2) ◽  
pp. 181-185 ◽  
Author(s):  
Hans Wadenvik ◽  
Ingrid Denfors ◽  
Jack Kutti

ScienceRise ◽  
2015 ◽  
Vol 6 (4 (11)) ◽  
pp. 25
Author(s):  
Алий Саитович Тугушев ◽  
Виталий Викторович Вакуленко ◽  
Ольга Степановна Черковская ◽  
Дмитрий Иванович Михантьев ◽  
Вячеслав Васильевич Нешта ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
Nicola Galea ◽  
Giulia Cundari ◽  
Cristian Borrazzo ◽  
Giacomo Pambianchi ◽  
Angelica Bracci ◽  
...  

The Cold Pressor Test (CPT) is a novel diagnostic strategy to noninvasively assess the myocardial microvascular endothelial-dependent function using perfusion magnetic resonance imaging (MRI). Spleen perfusion is modulated by a complex combination of several mechanisms involving the autonomic nervous system and vasoactive mediators release. In this context, the effects of cold temperature on splenic blood flow (SBF) still need to be clarified. Ten healthy subjects were studied by MRI. MRI protocol included the acquisition of GRE T1-weighted sequence (“first pass perfusion”) during gadolinium administration (0.1mmol/kg of Gd-DOTA at flow of 3.0 ml/s), at rest and after CPT. Myocardial blood flow (MBF) and SBF were measured by applying Fermi function deconvolution, using the blood pool input function sampled from the left ventricle cavity. MBF and SBF values after performing CPT were significantly higher than rest values (SBF at rest: 0.65 ± 0.15 ml/min/g Vs. SBF after CPT: 0.90 ± 0.14 ml/min/g, p: <0.001; MBF at rest: 0.90 ± 0.068 ml/min/g Vs. MBF after CPT: 1.22 ± 0.098 ml/min/g, p<0.005). Both SBF and MBF increased in all patients during the CPT. In particular, the CPT-induced increase was 43% ± 29% for SBF and 36.5% ± 17% for MBF. CPT increases SBF in normal subjects. The characterization of a standard perfusion response to cold might allow the use of the spleen as reference marker for the adequacy of cold stimulation during myocardial perfusion MRI.


Sign in / Sign up

Export Citation Format

Share Document