Dong E D, Han Q D
Institute of Vascular Medicine, Third Hospital, Beijing Medical University, China.
Zhongguo Yao Li Xue Bao. 1995 Nov;16(6):481-4.
To study the differences of the agonist-induced desensitization and the reserpinization-induced hypersensitization between alpha 1A- and alpha 1B-adrenoceptors (AR) mediated vasoconstriction.
The thoracic aortae, mesenteric, and renal arteries of rats were isolated. The cumulative-concentration response-curve (CCRC) of vasoconstriction for NE was recorded. NE activated only alpha 1-AR since the perfusing Krebs solution contained propranolol 1 mumol . L-1 and yohimbine 0.1 mumol . L-1 to block beta- and alpha 2-AR. CCRC for NE was made, preparations were pretreated with CEC 50 mumol . L-1 for then washed, and CCRC for NE was repeated. After i.p. reserpine 4 mg . g-1 i.p., the rats were killed, the thoracic aortae and renal arteries were taken, CCRC for NE was compared with the corresponding blood vessels in control rats.
Pretreatment with CEC caused reductions of the NE-induced maximal constriction by 82.5 +/- 3.0% (P < 0.01) and 54.2 +/- 9.5% (P < 0.01) in thoracic aortae and mesenteric arteries, respectively, but no effect in renal arteries. Preincubation with NE caused the alpha 1-AR mediated-vasoconstriction diminished 14.4 +/- 5.9, 1.8 +/- 0.8 and 7.3 +/- 1.8 times in aortae, renal arteries, and mesenteric arteries, respectively. In reserpinized rats, the contraction in renal arteries induced by NE increased by 56%, but showed no change in aortae.
Alpha 1B-AR mediated vasoconstriction is easier to be desensitized, while alpha 1A-AR mediated vasoconstriction is easier to be hypersensitized in rats.
研究α1A -和α1B -肾上腺素能受体(AR)介导的血管收缩中激动剂诱导的脱敏和利血平化诱导的超敏反应之间的差异。
分离大鼠胸主动脉、肠系膜动脉和肾动脉。记录去甲肾上腺素(NE)引起的血管收缩的累积浓度反应曲线(CCRC)。由于灌注的Krebs溶液含有1μmol·L-1的普萘洛尔和0.1μmol·L-1的育亨宾以阻断β -和α2 - AR,NE仅激活α1 - AR。制作NE的CCRC,用50μmol·L-1的CEC预处理制剂,然后冲洗,重复NE的CCRC。腹腔注射4mg·g-1利血平后,处死大鼠,取胸主动脉和肾动脉,将NE的CCRC与对照大鼠的相应血管进行比较。
CEC预处理分别使胸主动脉和肠系膜动脉中NE诱导的最大收缩降低82.5±3.0%(P<0.01)和54.2±9.5%(P<0.01),但对肾动脉无影响。NE预孵育使主动脉、肾动脉和肠系膜动脉中α1 - AR介导的血管收缩分别减弱14.4±5.9、1.8±0.8和7.3±1.8倍。在利血平化的大鼠中,NE诱导的肾动脉收缩增加了56%,但主动脉中无变化。
在大鼠中,α1B - AR介导的血管收缩更容易脱敏,而α1A - AR介导的血管收缩更容易超敏。