京都大学 / 0048 / 新制・課程博士 / 博士(薬科学) / 甲第21719号 / 薬科博第110号 / 新制||薬科||12(附属図書館) / 京都大学大学院薬学研究科医薬創成情報科学専攻 / (主査)教授 土居 雅夫, 教授 竹島 浩, 教授 中山 和久 / 学位規則第4条第1項該当 / Doctor of Pharmaceutical Sciences / Kyoto University / DFAM

A new approach to study angiotensin receptor distribution in the brain has been taken by developing antibodies to partial sequence of the angiotensin II (AII) type-1 receptor subtype (AT1) and demonstrating the presence of receptors with immunohistochemical staining. The antibody to a portion of the 3rd cytoplasmic loop of the AT1 receptor revealed distinctive punctate immunoreactive staining on cell bodies. The cell bodies were distributed in the forebrain in paraventricular and supraoptic nuclei, the organum vasculosum lamina terminalis, median preoptic area and subfornical organ. In the brainstem, the entire locus coeruleus was stained, together with the adjacent mesencephalic and motor nuclei of the trigeminal nerve. The auditory system including the cochlear nucleus and superior olivary nuclei were stained. In the medulla, all the structures involved in blood pressure control were stained including the nucleus of the solitary tract, the 12th nerve nuclei, the rostroventral lateral area and the nucleus ambiguous. Sites where AT2 receptors are located were not stained or staining was limited to specific area such as the medial accessory nucleus of the inferior olive. Immunocytochemical staining of AT1 receptors provides a new and more precise approach to the cellular localization of AII receptors.

The effect or indomethacin and its vehicle on blood pressure was studied in conscious rabbits during the infusion of three vasopressors. The cyclooxygenase inhibitor raised mean arterial pressure 12 (vehicle: 3) mm Hg during norepinephrine infusion, 5 (vehicle: 0) mm Hg during angioten- sin II infusion, and 5 (vehicle: −8) mm Hg during arginine vasopressin infusion. When saline was given in place of vasopressors, indomethacin failed to alter blood pressure. Since indomethacin elevated pressure in the presence, but not the absence, of all three vasopressors, the possibility that elevation of blood pressure per se stimulates synthesis of vasodilator prostaglandins was considered. A pressor action of indomethacin was observed in ganglion-blocked animals, in which absolute blood pressure remained below normotensive levels during angiotensin II infusion. Thus, indomethacin raised arterial pressure during the infusion of norepinephrine, angiotensin II, and vasopressin, and this action was not influenced by manipulation of blood pressure. These results suggest that each vasopressor promotes prostaglandin synthesis independently to a degree sufficient to restrain its pressor action.

The contribution of vasodilator prostaglandins and kinins to blood pressure regulation was studied during the infusion of different doses of angiotensin II in conscious rabbits. Angiotensin II was infused for 60 min. in each experiment. Indomethacin, a prostaglandin synthesis inhibitor, or Trasylol, a kallikrein inhibitor, was given at the 30 min. interval. Indomethacin caused a sustained increase in blood pressure during the infusion of pressor doses of angiotensin II. The range of the mean increase after prostaglandin synthesis inhibition was 3.4 to 6.0 and 3.0 to 9.4 mm Hg at angiotensin II infusion rates of 10 and 50 ng/kg/min respectively. In contrast, indomethacin did not alter blood pressure when the peptide was administered at subpressor levels. Trasylol did not alter blood pressure during infusion of angiotensin II. These results suggest that when blood pressure is maintained at supranormal levels by angiotensin II, the pressor action is attenuated by one or more prostaglandins; an event which is not mediated or assisted by changes in kinin metabolism

The occurrence of a functional intracellular renin-angiotensin system (RAS) has emerged as a new paradigm. Recently, we and others demonstrated intracellular synthesis of ANG II in cardiac myocytes and vascular smooth muscle cells that was dramatically stimulated in high glucose conditions. Cardiac fibroblasts significantly contribute to diabetes-induced diastolic dysfunction. The objective of the present study was to determine the existence of the intracellular RAS in cardiac fibroblasts and its role in extracellular matrix deposition. Neonatal rat ventricular fibroblasts were serum starved and exposed to isoproterenol or high glucose in the absence or presence of candesartan, which was used to prevent receptor-mediated uptake of ANG II. Under these conditions, an increase in ANG II levels in the cell lysate represented intracellular synthesis. Both isoproterenol and high glucose significantly increased intracellular ANG II levels. Confocal microscopy revealed perinuclear and nuclear distribution of intracellular ANG II. Consistent with intracellular synthesis, Western analysis showed increased intracellular levels of renin following stimulation with isoproterenol and high glucose. ANG II synthesis was catalyzed by renin and angiotensin-converting enzyme (ACE), but not chymase, as determined using specific inhibitors. High glucose resulted in increased transforming growth factor-β and collagen-1 synthesis by cardiac fibroblasts that was partially inhibited by candesartan but completely prevented by renin and ACE inhibitors. In conclusion, cardiac fibroblasts contain a functional intracellular RAS that participates in extracellular matrix formation in high glucose conditions, an observation that may be helpful in developing an appropriate therapeutic strategy in diabetic conditions.

No description available.

Hypertension, a risk factor for aortic valve stenosis, increases transvalvular load and can elicit extracellular matrix (ECM) remodeling. Elevated cyclic pressure and the vasoactive agent angiotensin II (Ang II) both promote collagen synthesis, an early hallmark of aortic sclerosis. It was hypothesized that increased collagen production induced by elevated pressure conditions or the presence of Ang II would affect the mechanical properties of leaflet tissue by decreasing extensibility. Porcine aortic valve leaflets were exposed to pressure conditions of increasing magnitude with and without Ang II. Biaxial mechanical testing was performed to determine peak stretch. Collagen content was determined using a quantitative dye-binding method. The results demonstrated Ang II and elevated pressure decrease the extensibility of leaflet tissue and increase the collagen content in the ECM. In conclusion, the results demonstrated that both elevated pressure and Ang II play a role in altering the biomechanical properties of aortic valve leaflets.

1. We studied the effect of intracellular angiotensin II (Ang II) and related peptides on rat aortic contraction, whether this effect is pharmacologically distinguishable from that induced by extracellular stimulation, and determined the Ca2+ source involved. 2. Compounds were delivered into the cytoplasm of de-endothelized aorta rings using multilamellar liposomes. Contractions were normalized to the maximum obtained with phenylephrine (10-5 M). 3. Intracellular administration of Ang II (incorporation range: 0.01-300 nmol mg-1) resulted in a dose-dependent contraction, insensitive to extracellular administration (10-6 M) of the AT1 receptor antagonist CV11947, the AT2 receptor antagonist PD 123319, or the non-selective AT receptor antagonist and partial agonist saralasin ([Sar1,Val5,Ala8]-Ang II (P < 0.05). 4. Intracellular administration of CV11947 or PD 123319 right shifted the dose-response curve about 1000 fold or 20 fold, respectively. PD 123319 was only effective if less than 30 nmol mg-1 Ang II was incorporated. 5. Contraction was partially desensitized to a second intracellular Ang II addition after 45 min (P < 0.05). 6. Intracellular administration of Ang I and saralasin also induced contraction (P < 0.05). Both responses were sensitive to intracellular CV11947 (P < 0.05), but insensitive to PD 123319. The response to Ang I was independent of intracellular captopril. 7. Contraction induced by extracellular application of Ang II and of Ang I was abolished by extracellular pre-treatment with saralasin or CV11947 (P < 0.05), but not with PD 123319. Extracellular saralasin induced no contraction. 8. Intracellular Ang II induced contraction was not affected by pre-treatment with heparin filled liposomes, but completely abolished in Ca2+-free external medium. 9. These results support the existence of an intracellular binding site for Ang II in rat aorta. Intracellular stimulation induces contraction dependent on Ca2+-influx but not on Ins(1,4,5)P3 mediated release from intracellular Ca2+-stores. Intracellular Ang I and saralasin induce contraction, possibly via the same binding site. Pharmacological properties of this putative intracellular receptor are clearly different from extracellular stimulated AT1 receptors or intracellular angiotensin receptors postulated in other tissue.

In Kardiomyozyten ist Calcium (Ca2+) ein wichtiges Signalmolekül und eine präzise Regulation der Ca2+ Konzentration in den Zellkompartimenten erforderlich. Ca2+ wird Angiotensin II-induziert und vom Botenstoff IP3 vermittelt aus IP3 Rezeptoren des Sarkoplasmatischen Retikulum (SR) freigesetzt, was zur mitochondrialen Ca2+ Aufnahme führt. Diese Kommunikationswege zwischen SR und Mitochondrium sind u.a. bei der Herzinsuffizienz durch pathologische Umbauprozesse gestört. Zudem zirkulieren bei Herzinsuffizienz vermehrt Hormone wie AngII, welches u.a. die intrazelluläre IP3 Konzentration steigert und als Hypertrophie Signal wirkt. Dieser Arbeit geht die Vermutung voraus, dass eine gestörte mitochondriale Ca2+ Aufnahme durch Veränderung des nukleären Ca2+ Transienten die hypertrophe Genexpression beeinflussen kann. Es wurde an ventrikulären Kardiomyozyten von adulten Mäusen mit kardiospezifischem MCU Knock out oder MCU Wildtyp untersucht, wie sich Ca2+ Transienten in Zytosol und Nukleus bei AngII-Stimulation und Störung der mitochondrialen Ca2+ Aufnahme durch Blockade des mRyR1 oder des MCU verändern. Zum Vergleich wurde der Effekt des β adrenerg vermittelten, IP3 unabhängigen Ca2+ Anstiegs beobachtet. Zur Untersuchung der Frequenzabhängigkeit der Effekte wurde die elektrische Stimulation wurde variiert. Die Arbeit zeigt, dass sich die Blockade der mitochondrialen Ca2+ Aufnahme unterschiedlich auf den nukleären Ca2+ Transienten auswirkt: Bei AngII-Stimulation kam es in Folge der Blockade des mRyR1, nicht aber des MCU, zur Steigerung des nukleären Ca2+ Transienten. Dieser Effekt war bei 1 Hz Stimulationsfrequenz, nicht aber nach einer Steigerung auf 4 Hz zu beobachten. Bei β adrenerger Stimulation hingegen veränderte die Blockade des MCU oder des mRyR1 die Ca2+ Transienten im Kern nicht signifikant. Die Arbeit verdeutlicht die Bedeutung der IP3 vermittelten Ca2+ Freisetzung für die Kontrolle der Ca2+ Konzentrationen in unterschiedlichen zellulären Kompartimenten. / Calcium (Ca2+) serves as a critical signaling molecule within cardiomyocytes, necessitating precise regulation of Ca2+ concentrations across cellular compartments. Angiotensin II (AngII) triggers Ca2+ release through inositol trisphosphate (IP3) receptors located on the sarcoplasmic reticulum (SR), a process mediated by the secondary messenger IP3, resulting in mitochondrial Ca2+ uptake. Perturbations in these communication pathways have been implicated in heart failure due to pathological remodeling processes. Additionally, in heart failure elevated levels of hormones like AngII have been observed, which increases intracellular IP3 concentration, thereby acting as a signal for hypertrophy. This work is based on the assumption that impaired mitochondrial Ca2+ uptake can influence hypertrophic gene expression by altering the nuclear Ca2+ transient. The investigation was conducted using ventricular cardiomyocytes obtained from adult mice with cardiac-specific MCU (mitochondrial calcium uniporter) knockout and MCU wildtype, analyzing alterations in cytosolic and nuclear Ca2+ transients upon AngII stimulation and impairment of mitochondrial Ca2+ uptake by blocking mRyR1 (ryanodine receptor) or MCU. Additionally, the impact of β-adrenergic mediated IP3-independent Ca2+ elevation was assessed, with varying electrical stimulation frequencies to explore frequency-dependent effects. The findings reveal distinct effects of mitochondrial Ca2+ uptake blockade on nuclear Ca2+ transients. While mRyR1 blockade, but not MCU blockade, augmented nuclear Ca2+ transients during AngII stimulation, this effect was evident at 1 Hz stimulation frequency and not after increase to 4 Hz. Conversely, β-adrenergic stimulation yielded no significant changes in nuclear Ca2+ transients upon MCU or mRyR1 blockade. This work underscores the significance of IP3-mediated Ca2+ release in controlling Ca2+ concentrations across diverse cellular compartments.

No description available.