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血栓素拮抗剂13-氮杂前列腺酸可抑制花生四烯酸诱导的离体血小板膜囊泡中Ca2+的释放。

The thromboxane antagonist, 13-azaprostanoic acid, inhibits arachidonic acid-induced Ca2+ release from isolated platelet membrane vesicles.

作者信息

Rybicki J P, Venton D L, Le Breton G C

出版信息

Biochim Biophys Acta. 1983 Mar 22;751(1):66-73. doi: 10.1016/0005-2760(83)90257-6.

DOI:10.1016/0005-2760(83)90257-6
PMID:6830832
Abstract

In the present study we investigated the ability of the arachidonic acid metabolites, prostaglandin H2 and thromboxane A2, to release Ca2+ from isolated platelet vesicles. The vesicles were prepared through modification of previously described procedures. 45Ca uptake and release were determined by Millipore filtration and isotope counting of the filter paper. Incubation of the vesicles (25 degrees C) with 50 microM CaCl2 (plus 45Ca) resulted in the accumulation of 13 nmol Ca2+ per mg of protein under steady-state conditions. Addition of arachidonic acid (25 microM) resulted in a 42% release of the accumulated Ca2+ and the production of 150 ng thromboxane B2/mg protein. Pretreatment of the vesicles with indomethacin (4 microM) completely inhibited arachidonic acid-induced Ca2+ release and reduced thromboxane B2 synthesis by 82%. Pretreatment of the vesicles with the specific thromboxane A2/prostaglandin H2 antagonist, 13-azaprostanoic acid (20 microM), also resulted in complete inhibition of Ca2+ release but no inhibition of thromboxane B2 production. Addition of prostaglandin H2 (0.3 microM) to the platelet vesicles produced a significant release of Ca2+ only in the presence of the adenylate cyclase inhibitor, 2',5'-dideoxyadenosine (100 microM). This Ca2+ release was totally blocked by 13-azaprostanoic acid (20 microM). The thromboxane synthetase inhibitor 9,11-azoprosta-5,13-dienoic acid (azo analog I, 3.6 microM), in the presence of 2',5'-dideoxyadenosine, only slightly inhibited Ca2+ release in response to added prostaglandin H2, even though thromboxane B2 production was blocked by 95%.

摘要

在本研究中,我们研究了花生四烯酸代谢产物前列腺素H2和血栓素A2从分离的血小板囊泡中释放Ca2+的能力。囊泡通过对先前描述的程序进行修改来制备。通过密理博过滤和滤纸的同位素计数来测定45Ca的摄取和释放。在稳态条件下,将囊泡(25℃)与50μM氯化钙(加45Ca)一起孵育,导致每毫克蛋白质积累13nmol Ca2+。添加花生四烯酸(25μM)导致积累的Ca2+释放42%,并产生150ng血栓素B2/毫克蛋白质。用吲哚美辛(4μM)预处理囊泡可完全抑制花生四烯酸诱导的Ca2+释放,并使血栓素B2合成减少82%。用特异性血栓素A2/前列腺素H2拮抗剂13-氮杂前列腺酸(20μM)预处理囊泡也导致Ca2+释放完全抑制,但不抑制血栓素B2的产生。仅在腺苷酸环化酶抑制剂2',5'-二脱氧腺苷(100μM)存在的情况下,向血小板囊泡中添加前列腺素H2(0.3μM)才会导致Ca2+的显著释放。这种Ca2+释放被13-氮杂前列腺酸(20μM)完全阻断。在2',5'-二脱氧腺苷存在的情况下,血栓素合成酶抑制剂9,11-氮杂前列腺-5,13-二烯酸(偶氮类似物I,3.6μM)仅略微抑制添加前列腺素H2后引起的Ca2+释放,尽管血栓素B2的产生被阻断了95%。

相似文献

1
The thromboxane antagonist, 13-azaprostanoic acid, inhibits arachidonic acid-induced Ca2+ release from isolated platelet membrane vesicles.血栓素拮抗剂13-氮杂前列腺酸可抑制花生四烯酸诱导的离体血小板膜囊泡中Ca2+的释放。
Biochim Biophys Acta. 1983 Mar 22;751(1):66-73. doi: 10.1016/0005-2760(83)90257-6.
2
Antagonism of thromboxane A2/prostaglandin H2 by 13-azaprostanoic acid prevents platelet deposition to the de-endothelialized rabbit aorta in vivo.
J Pharmacol Exp Ther. 1984 Apr;229(1):80-4.
3
13-Azaprostanoic acid: a specific antagonist of the human blood platelet thromboxane/endoperoxide receptor.13-氮杂前列腺酸:一种人血小板血栓素/内过氧化物受体的特异性拮抗剂。
Proc Natl Acad Sci U S A. 1979 Aug;76(8):4097-101. doi: 10.1073/pnas.76.8.4097.
4
Thromboxane A2/prostaglandin H2 mobilizes calcium in human blood platelets.血栓素A2/前列腺素H2可动员人血小板中的钙。
Am J Physiol. 1985 Jul;249(1 Pt 2):H1-7. doi: 10.1152/ajpheart.1985.249.1.H1.
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Specific binding of the thromboxane A2 antagonist 13-azaprostanoic acid to human platelet membranes.血栓素A2拮抗剂13-氮杂前列腺酸与人血小板膜的特异性结合。
Biochim Biophys Acta. 1983 Feb;728(2):171-8. doi: 10.1016/0005-2736(83)90468-6.
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Reversal of thromboxane A2/prostaglandin H2 and ADP-induced calcium release in intact platelets.完整血小板中血栓素A2/前列腺素H2及ADP诱导的钙释放的逆转
Am J Physiol. 1985 Jul;249(1 Pt 2):H8-13. doi: 10.1152/ajpheart.1985.249.1.H8.
7
Antagonism of prostaglandin-mediated responses in platelets and vascular smooth muscle by 13-azaprostanoic acid analogs. Evidence for selective blockade of thromboxane A2 responses.13-氮杂前列腺酸类似物对血小板和血管平滑肌中前列腺素介导反应的拮抗作用。血栓素A2反应选择性阻断的证据。
Biochem Pharmacol. 1985 Mar 1;34(5):641-7. doi: 10.1016/0006-2952(85)90258-8.
8
Investigation on a selective non-prostanoic thromboxane antagonist, BM 13.177, in human platelets.对一种选择性非前列腺素类血栓素拮抗剂BM 13.177在人血小板中的研究。
Thromb Res. 1984 Feb 1;33(3):277-88. doi: 10.1016/0049-3848(84)90163-4.
9
2-(6-carboxyhexyl)cyclopentanone hexylhydrazone: a potent inhibitor of the blood platelet cyclo-oxygenase.2-(6-羧基己基)环戊酮己基腙:一种有效的血小板环氧化酶抑制剂。
Prostaglandins. 1984 Apr;27(4):543-51. doi: 10.1016/0090-6980(84)90090-x.
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9,11-epoxyiminoprosta-5,13-dienoic acid is a thromboxane A2 antagonist in human platelets.9,11-环氧亚氨基前列腺-5,13-二烯酸是一种人血小板中的血栓素A2拮抗剂。
Nature. 1978 Oct 26;275(5682):764-6. doi: 10.1038/275764a0.

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J Cell Biol. 1985 Sep;101(3):993-1000. doi: 10.1083/jcb.101.3.993.
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Stimulus-response coupling in human platelets activated by monoclonal antibodies to the CD9 antigen, a 24 kDa surface-membrane glycoprotein.
由针对CD9抗原(一种24 kDa表面膜糖蛋白)的单克隆抗体激活的人血小板中的刺激-反应偶联。
Biochem J. 1990 Mar 1;266(2):527-35. doi: 10.1042/bj2660527.