Nowak G, Mogilnicka E
Pol J Pharmacol Pharm. 1985 Nov-Dec;37(6):765-72.
The effect of some beta-adrenoceptor agonists, such as clenbuterol, salbutamol, isoprenaline and formoterol on the NA turnover (estimated on the basis of NA disappearance after inhibition of its synthesis by FLA-63) in various regions of the rat brain was examined. All the used beta-agonists (given ip) accelerated the FLA-63 induced disappearance of NA in the cortex, limbic system and brain stem. That effect of the beta-agonists was antagonized by propranolol. The obtained results indicate that beta-adrenoceptors are involved in regulation of the NA turnover. After chronic treatment with salbutamol (5 mg/kg, twice a day for 10 days, the last dose--10 mg/kg), tolerance to acute affects of that substance developed. In turn, salbutamol given chronically prevented the clonidine-induced deceleration of NA disappearance. The effects observed after chronic salbutamol treatment may be due to developed adaptive changes in beta-, as well as in alpha 2-adrenoceptors.
研究了某些β-肾上腺素能受体激动剂,如克伦特罗、沙丁胺醇、异丙肾上腺素和福莫特罗对大鼠脑不同区域去甲肾上腺素(NA)周转(根据用FLA - 63抑制其合成后NA的消失情况估算)的影响。所有使用的β-激动剂(腹腔注射)均加速了FLA - 63诱导的皮质、边缘系统和脑干中NA的消失。β-激动剂的这种作用被普萘洛尔拮抗。所得结果表明β-肾上腺素能受体参与了NA周转的调节。用沙丁胺醇(5 mg/kg,每日两次,共10天,最后一剂为10 mg/kg)进行慢性治疗后,对该物质的急性作用产生了耐受性。反过来,长期给予沙丁胺醇可防止可乐定诱导的NA消失减慢。长期使用沙丁胺醇治疗后观察到的这些效应可能是由于β-肾上腺素能受体以及α2-肾上腺素能受体发生了适应性变化。