Kam Kenneth W L, Kravtsov Gennadi M, Liu Jing, Wong Tak Ming
Department of Physiology, Faculty of Medicine, the University of Hong Kong, Pokfulam, Hong Kong SAR, China.
Br J Pharmacol. 2005 Apr;144(7):972-81. doi: 10.1038/sj.bjp.0706123.
We previously showed that oestrogen confers cardioprotection by downregulating the cardiac beta1-adrenoceptor (beta1-AR). The present study examined the effect of oestrogen on the post beta1-AR signalling cascade, with particular emphasis on the activity of protein kinase A (PKA) and its influence on the L-type Ca2+ channel. Three groups of adult female Sprague-Dawley rats were used: sham-operated controls, bilaterally ovariectomized (Ovx) rats, and Ovx rats with oestrogen replacement (Ovx + E2), which restored the oestrogen concentration to normal. The electrically induced intracellular Ca2+ transient (E[Ca2+]i), 45Ca(2+)-uptake through cardiac L-type Ca2+ channels (Ca2+ channels), heart rate and force of contraction in response to beta-AR stimulation with 10 nM isoprenaline (Iso) in hearts from Ovx rats were significantly greater than those of control and Ovx + E2 rats. The basal and Iso-induced PKA activities were also higher in hearts from Ovx rats. KT5720, a selective PKA inhibitor, completely inhibited its potentiating effect on basal Ca2+ channel activity in the Ovx rat heart. On the other hand, expression of G proteins (G(alpha)s and G(alpha)i1-3)), basal and forskolin-stimulated cAMP accumulation, and responsiveness of PKA to cAMP, were not altered by Ovx. Interestingly, the PKA inhibitor at the same concentration significantly reduced the increases in PKA activity and Ca2+ channel activity upon beta-AR stimulation in all three groups of rats and the inhibitions were significantly greater in the Ovx rat than in the other two groups of rats. This study provides the first evidence that, in addition to downregulation of beta1-AR shown previously, suppression of PKA activity, which is partly responsible for the suppressed Ca2+ channel activity, also determines the E[Ca2+]i and cardiac contractility following beta-AR stimulation in the female rat.
我们之前表明,雌激素通过下调心脏β1 - 肾上腺素能受体(β1 - AR)发挥心脏保护作用。本研究检测了雌激素对β1 - AR信号转导级联反应的影响,特别关注蛋白激酶A(PKA)的活性及其对L型钙通道的影响。使用了三组成年雌性Sprague - Dawley大鼠:假手术对照组、双侧卵巢切除(Ovx)大鼠以及雌激素替代(Ovx + E2)的Ovx大鼠,后者使雌激素浓度恢复正常。在Ovx大鼠心脏中,用10 nM异丙肾上腺素(Iso)刺激β - AR后,电诱导的细胞内钙瞬变(E[Ca2 + ]i)、通过心脏L型钙通道(钙通道)的45Ca(2 + )摄取、心率和收缩力均显著高于对照组和Ovx + E2大鼠。Ovx大鼠心脏的基础PKA活性和Iso诱导的PKA活性也更高。选择性PKA抑制剂KT5720完全抑制了其对Ovx大鼠心脏基础钙通道活性的增强作用。另一方面,Ovx并未改变G蛋白(G(α)s和G(α)i1 - 3))的表达、基础和福斯可林刺激的cAMP积累以及PKA对cAMP的反应性。有趣的是,相同浓度的PKA抑制剂显著降低了三组大鼠β - AR刺激后PKA活性和钙通道活性的增加,且Ovx大鼠中的抑制作用明显大于其他两组大鼠。本研究首次提供证据表明,除了之前显示的β1 - AR下调外,PKA活性的抑制(部分负责钙通道活性的抑制)也决定了雌性大鼠β - AR刺激后的E[Ca2 + ]i和心脏收缩力。