Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO 65212, USA.
J Physiol. 2013 Mar 1;591(5):1251-63. doi: 10.1113/jphysiol.2012.244483. Epub 2012 Dec 17.
Abstract Mesenteric arteries (MAs) are studied widely in vitro but little is known of their reactivity in vivo. Transgenic animals have enabled Ca(2+) signalling to be studied in isolated MAs but the reactivity of these vessels in vivo is undefined. We tested the hypothesis that ageing alters MA reactivity to perivascular nerve stimulation (PNS) and adrenoreceptor (AR) activation during blood flow control. First- (1A), second- (2A) and third-order (3A) MAs of pentobarbital-anaesthetized Young (3-6 months) and Old (24-26 months) male and female Cx40(BAC)-GCaMP2 transgenic mice (C57BL/6 background; positive or negative for the GCaMP2 transgene) were studied with intravital microscopy. A segment of jejunum was exteriorized and an MA network was superfused with physiological salt solution (pH 7.4, 37°C). Resting tone was 10% in MAs of Young and Old mice; diameters were ∼5% (1A), 20% (2A) and 40% (3A) smaller (P 0.05) in Old mice. Throughout MA networks, vasoconstriction increased with PNS frequency (1-16 Hz) but was ∼20% less in Young vs. Old mice (P 0.05) and was inhibited by tetrodotoxin (1 μm). Capsaicin (10 μm; to inhibit sensory nerves) enhanced MA constriction to PNS (P 0.05) by ∼20% in Young but not Old mice. Phenylephrine (an α1AR agonist) potency was greater in Young mice (P 0.05) with similar efficacy (∼60% constriction) across ages and MA branches. Constrictions to UK14304 (an α2AR agonist) were less (∼20%; P 0.05) and were unaffected by ageing. Irrespective of sex or transgene expression, ageing consistently reduced the sensitivity of MAs to α1AR vasoconstriction while blunting the attenuation of sympathetic vasoconstriction by sensory nerves. These findings imply substantive alterations in splanchnic blood flow control with ageing.
摘要 肠系膜动脉(MAs)在体外研究广泛,但体内的反应性知之甚少。转基因动物使 Ca(2+)信号转导能够在分离的 MAs 中进行研究,但这些血管在体内的反应性尚不清楚。我们检验了这样一个假设,即衰老改变了血流控制时 PNS(perivascular nerve stimulation)和肾上腺素受体(adrenoreceptor,AR)激活对 MA 反应性。使用活体显微镜研究了戊巴比妥麻醉的年轻(3-6 个月)和年老(24-26 个月)雄性和雌性 Cx40(BAC)-GCaMP2 转基因小鼠(C57BL/6 背景;转基因组或非转基因组)的一级(1A)、二级(2A)和三级(3A)MA。将一段空肠引出并将 MA 网络用生理盐溶液(pH 7.4,37°C)灌流。年轻和年老小鼠的 MA 静息张力为 10%;直径分别减少 5%(1A)、20%(2A)和 40%(3A)(P 0.05)。在整个 MA 网络中,PNS 频率(1-16 Hz)增加导致血管收缩,但年轻小鼠的收缩幅度比年老小鼠小约 20%(P 0.05),并且被河豚毒素(1 μm)抑制。辣椒素(10 μm;抑制感觉神经)使 PNS 引起的 MA 收缩增加约 20%(P 0.05),但在年轻小鼠中而不是年老小鼠中。去氧肾上腺素(一种 α1AR 激动剂)在年轻小鼠中的效力更大(P 0.05),并且在各个年龄和 MA 分支中,其效果相似(约 60%的收缩)。UK14304(一种 α2AR 激动剂)引起的收缩较少(约 20%;P 0.05),并且不受衰老的影响。无论性别或转基因组的表达如何,衰老都持续降低 MA 对 α1AR 血管收缩的敏感性,同时减弱感觉神经对交感神经血管收缩的衰减。这些发现表明,随着年龄的增长,内脏血流控制发生了实质性的改变。