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衰老过程中以及慢性普萘洛尔治疗后大鼠下颌下腺中激动剂诱导的Ca2+动员。

Agonist-induced Ca2+ mobilization in the rat submandibular gland during aging and subsequent to chronic propranolol treatment.

作者信息

Melvin J E, O'Connell A C, Koek L, Bowen W H

机构信息

Department of Dental Research, University of Rochester, NY 14642.

出版信息

Mech Ageing Dev. 1991 Nov 15;61(1):33-44. doi: 10.1016/0047-6374(91)90005-k.

Abstract

The effects of age and chronic propranolol treatment on the agonist-induced rise in intracellular free Ca2+ ([Ca2+]i), an index for the coupling of receptor-second messenger generation, was studied using a dispersed rat submandibular gland preparation. Muscarinic stimulation (10 microns carbachol) caused a rapid (T1/2 less than 2 s) and dramatic (approximately 4.5-fold) rise in [Ca2+]i followed by a lower sustained increase (approximately 3-fold) in [Ca2+]i as measured directly with the Ca(2+)-sensitive fluorescent probe, fura-2. The magnitude and the rate of increase of the initial rise in [Ca2+]i and the level of the sustained increase in [Ca2+]i were not different between 2- an 21-month-old rats. Stimulation in a Ca(2+)-free medium reduced the initial agonist-induced increase in [Ca2+]i by approximately 35-40%, while the sustained increase was abolished by the removal of extracellular Ca2+ from cells in both young and old rats. Chronic treatment for 30 days with 20 mg/kg propranolol, a beta-adrenergic antagonist, did not significantly alter the ability of dispersed submandibular cells in old rats to mobilize Ca2+ during agonist stimulation or influence the in vivo stimulated gland output. These results suggest that the agonist-induced rise in [Ca2+]i is not altered by aging or by chronic treatment of aged rats with propranolol and, therefore, receptor-second messenger coupling remains intact.

摘要

利用大鼠颌下腺分散组织制备物,研究了年龄和慢性普萘洛尔治疗对激动剂诱导的细胞内游离钙离子浓度([Ca2+]i)升高的影响,[Ca2+]i是受体 - 第二信使生成偶联的一个指标。毒蕈碱刺激(10微摩尔卡巴胆碱)导致[Ca2+]i迅速(半衰期小于2秒)且显著(约4.5倍)升高,随后[Ca2+]i持续较低幅度升高(约3倍),这是通过钙敏感荧光探针fura - 2直接测量得到的。2月龄和21月龄大鼠在[Ca2+]i初始升高的幅度和速率以及[Ca2+]i持续升高的水平方面并无差异。在无钙培养基中刺激可使激动剂诱导的[Ca2+]i初始升高降低约35 - 40%,而在年轻和老年大鼠中,去除细胞外钙离子均可消除[Ca2+]i的持续升高。用β - 肾上腺素能拮抗剂普萘洛尔(20毫克/千克)进行30天的慢性治疗,并未显著改变老年大鼠分散颌下细胞在激动剂刺激期间动员钙离子的能力,也未影响体内刺激的腺体分泌。这些结果表明,激动剂诱导的[Ca2+]i升高不会因衰老或用普萘洛尔对老年大鼠进行慢性治疗而改变,因此,受体 - 第二信使偶联保持完整。

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