Alteration of reactivity in isolated mesenteric artery from Zucker fatty diabetes mellitus rats

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of pharmacological sciences Pub Date : 2024-06-27 DOI:10.1016/j.jphs.2024.06.006
Kosuke Otani, Naofumi Uemura, Hiroshi Funada, Tomoko Kodama, Muneyoshi Okada, Hideyuki Yamawaki
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Abstract

Obesity and diabetes are major risk factors for cardiovascular diseases. Zucker fatty diabetes mellitus (ZFDM) rats are novel animal model of obesity and type 2 diabetes. We have recently reported that blood pressure in ZFDM-Leprfa/fa (Homo) rats was normal, while blood adrenaline level and heart rate were lower than those in control ZFDM-Leprfa/+ (Hetero) rats. Here, we compared the reactivity in isolated mesenteric artery between Hetero and Homo rats. Contraction induced by phenylephrine was increased, while relaxation induced by isoprenaline was decreased in Homo rats at 21–23 weeks old compared with those in Hetero rats. The mRNA expression for α1A but not β2 adrenoreceptor in Homo rats was increased. Nitric oxide (NO)-mediated relaxation induced by acetylcholine was decreased, while the mRNA expression for endothelial NO synthase (eNOS) was rather increased in mesenteric artery from Homo rats. These findings for the first time revealed that in Homo rats with reduced plasma adrenaline, blood pressure could be maintained by enhancing vascular contractility induced by adrenaline through the increased α1 adrenoceptor expression and the attenuated β2 adrenoceptor signaling. Additionally, NO-mediated endothelium-dependent relaxation is impaired perhaps due to eNOS dysfunction, which might also contribute to maintain the blood pressure in Homo rats.

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扎克脂肪糖尿病大鼠离体肠系膜动脉反应性的改变
肥胖和糖尿病是心血管疾病的主要风险因素。扎克脂肪糖尿病(ZFDM)大鼠是肥胖和 2 型糖尿病的新型动物模型。我们最近报道了 ZFDM-Leprfa/fa(Homo)大鼠的血压正常,而血液肾上腺素水平和心率低于对照组 ZFDM-Leprfa/+(Hetero)大鼠。在此,我们比较了雌雄大鼠离体肠系膜动脉的反应性。与雌雄大鼠相比,21-23周龄的Homo大鼠由苯肾上腺素诱导的收缩增加,而由异丙肾上腺素诱导的松弛减少。同种大鼠α1A而非β2肾上腺素受体的 mRNA 表达增加。一氧化氮(NO)介导的乙酰胆碱松弛作用在同种大鼠肠系膜动脉中有所减弱,而内皮 NO 合酶(eNOS)的 mRNA 表达却有所增加。这些发现首次揭示了在血浆肾上腺素减少的同种大鼠中,肾上腺素可通过增加α1肾上腺素受体表达和减弱β2肾上腺素受体信号传导来增强血管收缩力,从而维持血压。此外,也许是由于 eNOS 功能障碍,NO 介导的内皮依赖性松弛功能受损,这也可能有助于维持同种大鼠的血压。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
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