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Platelets. 2017 Nov;28(7):698-705. doi: 10.1080/09537104.2016.1265920. Epub 2017 Feb 2.

Role of homocysteine and folic acid on the altered calcium homeostasis of platelets from rats with biliary cirrhosis.

Author information

1
a Depto. Fisiología, Fac. Medicina, Instituto Murciano de Investigación Biosanitaria (IMIB) , Universidad de Murcia, Murcia, Spain.
2
b Depto. Fisiología, Fac. Veterinaria , Universidad de Extremadura , Cáceres, Spain.

Abstract

Previously, we have found that intracellular calcium homeostasis is altered in platelets from an experimental model of liver cirrhosis, the bile-duct ligated (BDL) rat; these alterations are compatible with the existence of a hypercoagulable state. Different studies indicate that cholestatic diseases are associated with hyperhomocysteinemia; thus, we hypothetized that it could contribute to those platelet alterations. In the present study, we have investigated the role of homocysteine (HCY) in platelet aggregation and calcium signaling in the BDL model. The effect of chronic folic acid treatment was also analyzed. Acute treatment with HCY increased the aggregation response to ADP and calcium responses to thrombin in platelets of control and BDL rats. Capacitative calcium entry was not altered by HCY. Chronic treatment with folic acid decreased platelet aggregation in control and BDL rats, but this decrease was greater in BDL rats. In folic acid-treated rats, thrombin-induced calcium entry and release were decreased in platelet of control rats but unaltered in BDL rats; however, capacitative calcium entry was decreased in platelets of control and BDL rats treated with folic acid. Reactive oxygen species were produced at higher levels by BDL platelets after stimulation with HCY or thrombin and folic acid normalized these responses. HCY plays a role in the enhanced platelet aggregation response of BDL rats, probably through an enhanced formation of ROS. Folic acid pretreatment normalizes many of the platelet alterations shown by BDL rats.

KEYWORDS:

Bile-duct ligation; calcium signaling; capacitative Ca2+ entry; cholestasis; fura-2; liver cirrhosis; thapsigargin; thrombin

PMID:
28150525
DOI:
10.1080/09537104.2016.1265920
[Indexed for MEDLINE]

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