Inositol 1,4,5-trisphosphate formation, cytoplasmic calcium dynamics, and alpha-amylase secretion of pancreatic acini isolated from aged and chronically alcohol-fed rats.

E Siegmund, H Pommerenke, L Jonas, H Nizze, I Höllerich, A Röhring, P Schuff-Werner
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引用次数: 3

Abstract

Methods: Three-month-old female Wistar rats were fed with 20% alcohol in their drinking fluid over 6-17 mo using an interrupted feeding regimen. At different times, pancreatic acini were isolated by mild collagenase digestion. The concentrations of inositol-1,4,5-trisphosphate (1,4,5-IP3) were determined by a specific radioreceptor assay, before and at different times after stimulation with varying concentrations of CCK-8. CCK-induced dynamics of cytoplasmic calcium ([Ca2+]c) was investigated in acinar cells by confocal laser raster microscopy. Acinar alpha-amylase (Aml) secretion was measured as enzyme activity in the medium compared to the total activity in the suspension.

Results: In 12-13-mo-old rats, the CCK-stimulated 1,4,5-IP3 formation in acini was found to be decreased compared to young rats (age 4 mo). In rats of the same age fed with ethanol from the age of 3 mo on, 1,4,5-IP3 concentrations in acini were higher and reached values comparable to those in young rats. Correspondingly, the CCK-induced [Ca2+]c dynamics in acini isolated from 9-mo-old rats was impaired compared to that of young rats but normal in aged, chronically alcohol-fed rats. Aml secretion under CCK stimulation, however, which was decreased in aged rats, was additionally impaired after alcohol feeding.

Conclusion: Chronic alcohol feeding modifies 1,4,5-IP3 formation, the [Ca2+]c dynamics of, and the Aml secretion of rat pancreatic acini in response to CCK stimulation. Obviously, the age-related impairment of 1,4,5-IP3 formation and [Ca2+]c dynamics is improved. In contrast, the decrease in Aml secretion of acini isolated from aged rats is more pronounced after long-term alcohol-feeding.

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老年和慢性酒精喂养大鼠胰腺腺泡中肌醇1,4,5-三磷酸形成、细胞质钙动力学和α -淀粉酶分泌
方法:3月龄Wistar雌性大鼠在6-17个月的时间里,采用中断喂养的方法,在饮水液中添加20%的酒精。在不同的时间,用温和的胶原酶消化法分离胰腺腺泡。在不同浓度CCK-8刺激前后的不同时间,通过特定的放射受体测定肌醇-1,4,5-三磷酸(1,4,5- ip3)的浓度。用共聚焦激光光栅显微镜研究了cck诱导的胞质钙([Ca2+]c)的动态变化。通过与悬液中总活性的比较,测定培养基中腺泡α -淀粉酶(Aml)的分泌。结果:在12-13月龄大鼠中,cck刺激的腺泡中1,4,5- ip3的形成与幼鼠(4月龄)相比有所减少。相同年龄的大鼠,从3月龄开始用乙醇喂养,腺泡中的1,4,5- ip3浓度较高,达到与幼鼠相当的值。相应地,与年轻大鼠相比,从9岁大鼠分离的cck诱导的[Ca2+]c动态受损,但在老年长期饮酒大鼠中正常。然而,在CCK刺激下,老年大鼠的Aml分泌减少,在酒精喂养后也受到损害。结论:慢性酒精喂养改变CCK刺激下大鼠胰腺腺泡的1,4,5- ip3形成、[Ca2+]c动态和Aml分泌。显然,年龄相关的1,4,5- ip3形成和[Ca2+]c动力学损伤得到改善。相比之下,老年大鼠分离的acini分泌Aml的减少在长期酒精喂养后更为明显。
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