Fernley R T, Wright R D, Coghlan J P
Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.
Biochem J. 1991 Mar 1;274 ( Pt 2)(Pt 2):313-6. doi: 10.1042/bj2740313.
A specific and sensitive radioimmunoassay has been developed for the measurement of the secreted carbonic anhydrase isoenzyme (CA VI) in sheep saliva and tissues. The assay can detect as little as 75 pg of CA VI, and the antibody used does not cross-react with CA II or CA III. The intra-assay variation, measured using a saliva sample, was 3.0%, whereas the inter-assay variation was 10.5%. The concentration of CA VI in parotid saliva from normal, resting sheep was 5.6 +/- 3.0 micrograms.ml-1 (n = 42) or 79.4 +/- 35.7 micrograms.mg of total protein-1. With feeding, the CA VI concentrations increased an average of 6-fold. The secretion rate of CA VI from the vascularly isolated neurotomized parotid gland of the anaesthetized sheep was 0.62 +/- 0.40 micrograms.min-1, compared with a rate of 11.7 +/- 7.8 micrograms.min-1 from the parotid gland of normal conscious sheep. Stimulation of the parotid-gland preparation by the muscarinic agent bethanechol increased the secretion rate to 438 +/- 172 microgram.min-1 (n = 8), and electrical stimulation of the secretomotor Moussu nerve increased CA VI secretion rate to 634 +/- 330 micrograms.min-1 (n = 4). Submandibular saliva from anaesthetized sheep contained 6.9 +/- 2.1 micrograms of CA VI.ml-1 (n = 3). The only tissues found to contain measurable amounts of CA VI were the parotid (6.4 micrograms.mg of protein-1) and submandibular (1.8 micrograms.mg of protein-1) salivary glands. The sublingual salivary gland, kidney, lung, adrenal, brain, skeletal muscle, liver, heart, pancreas, small intestine and cerebrospinal fluid did not have a measurable CA VI content.
已开发出一种特异性和敏感性高的放射免疫分析法,用于测定绵羊唾液和组织中分泌的碳酸酐酶同工酶(CA VI)。该分析法可检测低至75 pg的CA VI,所用抗体与CA II或CA III无交叉反应。使用唾液样本测得的批内变异为3.0%,而批间变异为10.5%。正常、静息绵羊腮腺唾液中CA VI的浓度为5.6±3.0μg·ml-1(n = 42)或79.4±35.7μg·mg总蛋白-1。进食时,CA VI浓度平均增加6倍。麻醉绵羊经血管分离并切断神经支配的腮腺中CA VI的分泌速率为0.62±0.40μg·min-1,而正常清醒绵羊腮腺的分泌速率为11.7±7.8μg·min-1。毒蕈碱剂氨甲酰甲胆碱刺激腮腺制剂可使分泌速率增加至438±172μg·min-1(n = 8),而电刺激分泌运动的穆苏神经可使CA VI分泌速率增加至634±330μg·min-1(n = 4)。麻醉绵羊下颌下唾液中含6.9±2.1μg CA VI·ml-1(n = 3)。发现唯一含有可测量量CA VI的组织是腮腺(6.4μg·mg蛋白-1)和下颌下腺(1.8μg·mg蛋白-1)。舌下腺、肾脏、肺、肾上腺、脑、骨骼肌、肝脏、心脏、胰腺、小肠和脑脊液中CA VI含量不可测。