Short-Term in Situ Effects of Prolactin and Insulin on Ion Transport in Liver and Intestine of Freshwater Climbing Perch ( Anabas testudineus Bloch)

M. Peter, V. Mini, D. S. Bindulekha, V. S. Peter
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引用次数: 2

Abstract

The short-term in situ effects of prolactin and insulin on the transport of monovalent and divalent cations were examined in climbing perch Anabas testudineus to infer upon how these hormones regulate ion transport in the metabolic and osmoregualtory tissues of freshwater fish. Varied doses (10 -9 , 10 -8 and 10 -7 M) of ovine prolactin (oPRL) and insulin were infused in these fish for 20 min and the specific activities of ion-specific ATPases were analyzed. The Na + , K + -ATPase activity in the intestine and liver showed significant increase after oPRL infusion. Infusion of oPRL significantly decreased the cytosolic H + -ATPase activity in the intestine and liver, but increased the cytosolic Ca 2+ -ATPase activity in these tissues. Infusion of oPRL decreased the mitochondrial Mg 2+ -ATPase and H + -ATPase activities in the liver but the activities of these transporters increased in the intestine. Similar to oPRL, insulin infusion produced dose-dependent effects on the transporter activities in the liver and intestinal tissues. The mitochondrial Mg 2+ -ATPase activity in the liver significantly decreased at 10 -9 and 10 -7 M insulin infusion whereas its activity increased significantly in intestine at 10 -8 M insulin. Likewise, insulin infusion produced significant increases in the activities of all tested transporters except the cytosolic H + -ATPase activity in the intestine. A direct action of insulin on ion transport was found in both liver and intestinal tissues, as evident in the activity patterns of ion-specific ATPases. Taken together the results point to vital roles of PRL and insulin in ion transport in both liver and intestinal tissues of climbing perch.
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催乳素和胰岛素对淡水攀鲈肝脏和肠道离子转运的短期原位影响
研究了催乳素和胰岛素对龙尾鲈鱼一价和二价阳离子运输的短期原位影响,以推断这些激素如何调节淡水鱼代谢和渗透组织中的离子运输。将不同剂量(10 -9、10 -8和10 -7 M)的绵羊催乳素(oPRL)和胰岛素注入这些鱼体内20 min,分析离子特异性atp酶的特异性活性。oPRL输注后,小肠和肝脏内Na +、K + - atp酶活性显著升高。灌注oPRL可显著降低肠、肝组织胞浆中H + -ATPase活性,但提高这些组织胞浆中ca2 + -ATPase活性。输注oPRL降低了肝脏线粒体Mg 2+ - atp酶和H + - atp酶活性,但增加了肠道转运体活性。与oPRL相似,胰岛素输注对肝脏和肠道组织的转运蛋白活性产生剂量依赖效应。胰岛素注射10 -9和10 -7 M时,肝脏线粒体Mg 2+ - atp酶活性显著降低,而胰岛素注射10 -8 M时,肠道线粒体Mg 2+ - atp酶活性显著升高。同样,胰岛素输注显著增加了除肠内胞浆H + - atp酶活性外的所有被测转运蛋白的活性。在肝脏和肠道组织中发现了胰岛素对离子运输的直接作用,这在离子特异性atp酶的活性模式中是显而易见的。综上所述,这些结果表明PRL和胰岛素在攀鲈肝脏和肠道组织的离子运输中起着重要作用。
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