scholarly journals Effect of EGTA on serotonin transport into blood platelets.

1993 ◽  
Vol 61 ◽  
pp. 151
Author(s):  
Ken-ichi Nezasa ◽  
Hiroaki Nishio ◽  
Yoshihiro Nakata
1995 ◽  
Vol 10 (7) ◽  
pp. 352-354 ◽  
Author(s):  
I Modai ◽  
A Valevski ◽  
L Kikinzon ◽  
Z Jerushalmy ◽  
A Weizman

SummaryIt has been suggested that low serum cholesterol interferes with brain serotonergic functioning, which results in increased suicidal and aggressive tendencies. To test this hypothesis we investigated the relationship between serum cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL) and triglyceride levels, and serotonin uptake by blood platelets in 17 healthy men aged 39.5 ± 10.2 years. Platelet serotonin uptake and serum lipids were assayed concomitantly for each individual. Serum cholesterol levels and other serum lipid levels did not correlate with serotonin uptake by platelets at the concentration of 2 × 10−5 M (a concentration within the maximal uptake capacity range). The results indicate no influence of cholesterol on serotonin uptake, as opposed to some investigators who suggested that high risk of suicide and aggressiveness in hypocholesterolemic individuals is related to impaired serotonin transport.


1977 ◽  
Vol 26 (18) ◽  
pp. 1645-1655 ◽  
Author(s):  
Hans-Joachim Reimers ◽  
David J. Allen ◽  
Jean-Pierre Cazenave ◽  
Irwin A. Feuerstein ◽  
J. Fraser Mustard

2019 ◽  
Vol 151 (11) ◽  
pp. 1248-1264 ◽  
Author(s):  
Gary Rudnick ◽  
Walter Sandtner

Serotonin (5-hydroxytryptamine [5-HT]) is accumulated within nerve endings by the serotonin transporter (SERT), which terminates its extracellular action and provides cytoplasmic 5-HT for refilling of synaptic vesicles. SERT is the target for many antidepressant medications as well as psychostimulants such as cocaine and ecstasy (3,4-methylenedioxymethamphetamine). SERT belongs to the SLC6 family of ion-coupled transporters and is structurally related to several other transporter families. SERT was studied in the 1970s and 1980s using membrane vesicles isolated from blood platelets. These studies led to a proposed stoichiometry of transport that has been challenged by high-resolution structures of SERT and its homologues and by studies of SERT electrophysiology. Here, we review the original evidence alongside more recent structural and electrophysiological evidence. A self-consistent picture emerges with surprising insights into the ion fluxes that accompany 5-HT transport.


1959 ◽  
Vol 197 (1) ◽  
pp. 81-84 ◽  
Author(s):  
I. Sano ◽  
Y. Kakimoto ◽  
K. Taniguchi ◽  
M. Takesada

An active transport of serotonin was demonstrated in a previous report from this laboratory on rabbit blood platelets. Epinephrine is known to be taken up by the blood platelets as serotonin when the cells are suspended in plasma. In this paper evidence of an active transport of epinephrine is presented. The absorption of this amine is the movement into the cell against a concentration gradient. Epinephrine added to the suspending medium accumulated in the cells, after 1 hour's incubation at 37°C, when glucose or its metabolites were present. The concentration of the amine rose to 1 or 2 µg from about 0.005 µg/mg dry weight of platelets. Glucose, pyruvate, acetate, α-ketoglutarate and fumarate were the effective stimulators. The effect of glucose was diminished by the presence of sodium fluoride, iodoacetate, 2,4-dinitrophenol and reserpine. Competitive inhibitions of the active transport by aromatic compounds containing ethylamine groups might suggest the participation of the amine group of epinephrine in its transport. In contrast, serotonin transport was inhibited by a 5-hydroxyindol compound.


Author(s):  
E. T. O'Toole ◽  
R. R. Hantgan ◽  
J. C. Lewis

Thrombocytes (TC), the avian equivalent of blood platelets, support hemostasis by aggregating at sites of injury. Studies in our lab suggested that fibrinogen (fib) is a requisite cofactor for TC aggregation but operates by an undefined mechanism. To study the interaction of fib with TC and to identify fib receptors on cells, fib was purified from pigeon plasma, conjugated to colloidal gold and used both to facilitate aggregation and as a receptor probe. Described is the application of computer assisted reconstruction and stereo whole mount microscopy to visualize the 3-D organization of fib receptors at sites of cell contact in TC aggregates and on adherent cells.Pigeon TC were obtained from citrated whole blood by differential centrifugation, washed with Ca++ free Hank's balanced salts containing 0.3% EDTA (pH 6.5) and resuspended in Ca++ free Hank's. Pigeon fib was isolated by precipitation with PEG-1000 and the purity assessed by SDS-PAGE. Fib was conjugated to 25nm colloidal gold by vortexing and the conjugates used as the ligand to identify fib receptors.


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