Suppr超能文献

大鼠心脏中存在局部激肽释放酶-激肽系统。

A local kallikrein-kinin system is present in rat hearts.

作者信息

Nolly H, Carbini L A, Scicli G, Carretero O A, Scicli A G

机构信息

Hypertension and Vascular Research Division, Henry Ford Hospital, Detroit, MI 48202.

出版信息

Hypertension. 1994 Jun;23(6 Pt 2):919-23. doi: 10.1161/01.hyp.23.6.919.

Abstract

It has been reported that kinins mediate part of the beneficial cardiac effects induced by treatment with angiotensin-converting enzyme inhibitors in situations such as ischemia-reperfusion injury, myocardial infarction, and cardiac hypertrophy. However, it is not known whether the heart contains an independent kallikrein-kinin system. We measured kallikrein in tissue and in the incubation medium of heart slices. Heart slices released active and total (trypsin-activatable) kallikrein into the medium (46 +/- 5 and 380 +/- 18 pg bradykinin/mg, respectively, after 1 hour and 78 +/- 6 and 654 +/- 14 pg bradykinin/mg after 2 hours, n = 7). Release was not due to tissue damage because lactate dehydrogenase, a cytosolic marker, decreased from 8.9 +/- 2.9 to 2.9 +/- 1.0 U/mg per hour. Although kallikrein was released, total tissue kallikrein in the slices did not change (423 +/- 25 pg bradykinin/mg in nonincubated slices and 370 +/- 42 pg bradykinin/mg after 2 hours, P = NS), suggesting pool replenishment. Cardiac kallikrein activity was inhibited by incubation with anti-glandular kallikrein antibodies. Pretreatment with the protein synthesis inhibitor puromycin (10 mg IP) lowered release of active kallikrein from 78 +/- 6 to 22 +/- 4 pg bradykinin/mg and total kallikrein from 654 +/- 14 to 113 +/- 9 pg bradykinin/mg (P < .001). By using reverse transcription polymerase chain reaction with kallikrein family oligonucleotide primers and a specific kallikrein probe, we found that mRNA for tissue kallikrein is present in both atrial and ventricular RNA. Kallikrein activity was also detected in primary cultures of neonatal rat atrial and ventricular cardiocytes and their incubation medium.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

据报道,在缺血再灌注损伤、心肌梗死和心肌肥大等情况下,激肽介导了血管紧张素转换酶抑制剂治疗所诱导的部分有益心脏效应。然而,心脏是否含有独立的激肽释放酶-激肽系统尚不清楚。我们测量了心脏切片组织及其孵育培养基中的激肽释放酶。心脏切片将活性和总(胰蛋白酶可激活)激肽释放酶释放到培养基中(1小时后分别为46±5和380±18 pg缓激肽/毫克,2小时后为78±6和654±14 pg缓激肽/毫克,n = 7)。释放并非由于组织损伤,因为作为胞质标志物的乳酸脱氢酶每小时从8.9±2.9降至2.9±1.0 U/毫克。尽管激肽释放酶被释放,但切片中的总组织激肽释放酶没有变化(未孵育切片中为423±25 pg缓激肽/毫克,2小时后为370±42 pg缓激肽/毫克,P =无显著差异),提示储备补充。心脏激肽释放酶活性通过与抗腺性激肽释放酶抗体孵育而受到抑制。用蛋白质合成抑制剂嘌呤霉素(10毫克腹腔注射)预处理可使活性激肽释放酶的释放从78±6降至22±4 pg缓激肽/毫克,总激肽释放酶从654±14降至113±9 pg缓激肽/毫克(P <.001)。通过使用激肽释放酶家族寡核苷酸引物和特异性激肽释放酶探针进行逆转录聚合酶链反应,我们发现组织激肽释放酶的mRNA存在于心房和心室RNA中。在新生大鼠心房和心室心肌细胞的原代培养物及其孵育培养基中也检测到了激肽释放酶活性。(摘要截短于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验