M J García-Barrado, C Sancho, J Palomero, J Moratinos
{"title":"α 2-肾上腺素受体在兔α 1-和β -肾上腺素受体刺激引起的高血糖和胰岛素分泌效应中的作用。","authors":"M J García-Barrado, C Sancho, J Palomero, J Moratinos","doi":"10.1046/j.1365-2680.1998.18596.x","DOIUrl":null,"url":null,"abstract":"<p><p>1. In conscious fasted rabbits the insulin secretory response induced by the intravenous infusion of the alpha1-adrenoceptor agonist, amidephrine (10 microg kg(-1) min(-1)) was blocked by the simultaneous administration of clonidine (2 microg kg(-1) min(-1) i.v.). 2. The excitatory effect of amidephrine (10 microg kg(-1) min(-1)) on insulin secretion was similarly suppressed by the concomitant infusion of the selective alpha2-adrenoceptor agonist UK14304 (1 microg kg(-1) min(-1)). Both, the increase in blood glucose and the inhibition of insulin secretion found with UK14304 when infused alone were antagonized in rabbits previously treated with the very selective alpha2-adrenoceptor antagonist 2-methoxyidazoxan (1.5 microg kg(-1) min(-1)). 3. The combined administration of amidephrine (3 microg kg(-1) min(-1)) and isoprenaline (0.3 microg kg(-1) min(-1)) evoked a potentiated increase in insulin plasma levels in the face of a weak hyperglycaemia, an established reduction in blood pressure and tachycardia. 4. The potentiated insulin secretory response derived from alpha1- and beta-adrenoceptor stimulation was blunted by clonidine administration. In its presence a sustained hyperglycaemic response was found. 5. The increase in plasma lactate levels resulting from dual adrenoceptor stimulation (amidephrine: 10 microg kg(-1) min(-1) + salbutamol: 0.3 microg kg(-1) min(-1)) was smaller than the expected should addition or potentiation occurred. 6. Our results point to a possible physiological role played by alpha2-adrenoceptors on insulin secretion, since their stimulation by the endogenous catecholamines could lead to inhibition of insulin release, masking any potentiated response that otherwise should have appeared from alpha1- and beta-adrenoceptor stimulation.</p>","PeriodicalId":15103,"journal":{"name":"Journal of autonomic pharmacology","volume":"18 5","pages":"287-95"},"PeriodicalIF":0.0000,"publicationDate":"1998-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"12","resultStr":"{\"title\":\"Role of alpha2-adrenoceptors on the hyperglycaemic and insulin secretory effects derived from alpha1- and beta-adrenoceptor stimulation in the rabbit.\",\"authors\":\"M J García-Barrado, C Sancho, J Palomero, J Moratinos\",\"doi\":\"10.1046/j.1365-2680.1998.18596.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>1. In conscious fasted rabbits the insulin secretory response induced by the intravenous infusion of the alpha1-adrenoceptor agonist, amidephrine (10 microg kg(-1) min(-1)) was blocked by the simultaneous administration of clonidine (2 microg kg(-1) min(-1) i.v.). 2. The excitatory effect of amidephrine (10 microg kg(-1) min(-1)) on insulin secretion was similarly suppressed by the concomitant infusion of the selective alpha2-adrenoceptor agonist UK14304 (1 microg kg(-1) min(-1)). Both, the increase in blood glucose and the inhibition of insulin secretion found with UK14304 when infused alone were antagonized in rabbits previously treated with the very selective alpha2-adrenoceptor antagonist 2-methoxyidazoxan (1.5 microg kg(-1) min(-1)). 3. The combined administration of amidephrine (3 microg kg(-1) min(-1)) and isoprenaline (0.3 microg kg(-1) min(-1)) evoked a potentiated increase in insulin plasma levels in the face of a weak hyperglycaemia, an established reduction in blood pressure and tachycardia. 4. The potentiated insulin secretory response derived from alpha1- and beta-adrenoceptor stimulation was blunted by clonidine administration. In its presence a sustained hyperglycaemic response was found. 5. The increase in plasma lactate levels resulting from dual adrenoceptor stimulation (amidephrine: 10 microg kg(-1) min(-1) + salbutamol: 0.3 microg kg(-1) min(-1)) was smaller than the expected should addition or potentiation occurred. 6. 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引用次数: 12
摘要
1. 在清醒禁食的家兔中,静脉输注α -肾上腺素受体激动剂氨基肾上腺素(10 μ g kg(-1) min(-1))诱导的胰岛素分泌反应被同时给予可乐定(2 μ g kg(-1) min(-1)静脉注射)阻断。2. 同样,同时输注选择性α 2-肾上腺素受体激动剂UK14304 (1 μ g kg(-1) min(-1))也能抑制氨基肾上腺素(10 μ g kg(-1) min(-1))对胰岛素分泌的兴奋作用。单独输注UK14304时发现的血糖升高和胰岛素分泌抑制作用,在兔先前用非常选择性的α 2-肾上腺素能受体拮抗剂2-甲氧基唑嗪(1.5 μ g kg(-1) min(-1))治疗的情况下被拮抗。3.联合给药氨基肾上腺素(3 μ g kg(-1) min(-1))和异丙肾上腺素(0.3 μ g kg(-1) min(-1))在面对弱高血糖时引起胰岛素血浆水平的增强,血压和心动过速的既定降低。4. 由α - 1和β -肾上腺素能受体刺激引起的胰岛素分泌反应被可乐定抑制。在它的存在下发现了持续的高血糖反应。5. 双肾上腺素受体刺激引起的血浆乳酸水平升高(氨基肾上腺素:10微克kg(-1)分钟(-1)+沙丁胺醇:0.3微克kg(-1)分钟(-1))小于预期的增加或增强。6. 我们的研究结果表明,由于内源性儿茶酚胺对α - 2肾上腺素受体的刺激可能导致胰岛素释放的抑制,从而掩盖了α - 1和β -肾上腺素受体刺激可能产生的任何增强反应,因此α - 2肾上腺素受体在胰岛素分泌中可能发挥的生理作用。
Role of alpha2-adrenoceptors on the hyperglycaemic and insulin secretory effects derived from alpha1- and beta-adrenoceptor stimulation in the rabbit.
1. In conscious fasted rabbits the insulin secretory response induced by the intravenous infusion of the alpha1-adrenoceptor agonist, amidephrine (10 microg kg(-1) min(-1)) was blocked by the simultaneous administration of clonidine (2 microg kg(-1) min(-1) i.v.). 2. The excitatory effect of amidephrine (10 microg kg(-1) min(-1)) on insulin secretion was similarly suppressed by the concomitant infusion of the selective alpha2-adrenoceptor agonist UK14304 (1 microg kg(-1) min(-1)). Both, the increase in blood glucose and the inhibition of insulin secretion found with UK14304 when infused alone were antagonized in rabbits previously treated with the very selective alpha2-adrenoceptor antagonist 2-methoxyidazoxan (1.5 microg kg(-1) min(-1)). 3. The combined administration of amidephrine (3 microg kg(-1) min(-1)) and isoprenaline (0.3 microg kg(-1) min(-1)) evoked a potentiated increase in insulin plasma levels in the face of a weak hyperglycaemia, an established reduction in blood pressure and tachycardia. 4. The potentiated insulin secretory response derived from alpha1- and beta-adrenoceptor stimulation was blunted by clonidine administration. In its presence a sustained hyperglycaemic response was found. 5. The increase in plasma lactate levels resulting from dual adrenoceptor stimulation (amidephrine: 10 microg kg(-1) min(-1) + salbutamol: 0.3 microg kg(-1) min(-1)) was smaller than the expected should addition or potentiation occurred. 6. Our results point to a possible physiological role played by alpha2-adrenoceptors on insulin secretion, since their stimulation by the endogenous catecholamines could lead to inhibition of insulin release, masking any potentiated response that otherwise should have appeared from alpha1- and beta-adrenoceptor stimulation.