본문 바로가기
HOME> 논문 > 논문 검색상세

논문 상세정보

Frontiers in physiology v.9, 2018년, pp.231 -    SCIE
본 등재정보는 저널의 등재정보를 참고하여 보여주는 베타서비스로 정확한 논문의 등재여부는 등재기관에 확인하시기 바랍니다.

Circadian Differences in the Contribution of the Brain Renin-Angiotensin System in Genetically Hypertensive Mice

Jackson, Kristy L.    (Neuropharmacology Laboratory, Baker Heart and Diabetes Research Institute , Melbourne, VIC , Australia  ); Marques, Francine Z.    (Department of Pharmacology, Monash University , Victoria, VIC , Australia  ); Lim, Kyungjoon    (Neuropharmacology Laboratory, Baker Heart and Diabetes Research Institute , Melbourne, VIC , Australia  ); Davern, Pamela J.    (Neuropharmacology Laboratory, Baker Heart and Diabetes Research Institute , Melbourne, VIC , Australia  ); Head, Geoffrey A.    (Neuropharmacology Laboratory, Baker Heart and Diabetes Research Institute , Melbourne, VIC , Australia  );
  • 초록  

    Objective: Genetically hypertensive BPH/2J mice are recognized as a neurogenic model of hypertension, primarily based on sympathetic overactivity and greater neuronal activity in cardiovascular regulatory brain regions. Greater activity of the central renin angiotensin system (RAS) and reactive oxygen species (ROS) reportedly contribute to other models of hypertension. Importantly the peripheral RAS contributes to the hypertension in BPH/2J mice, predominantly during the dark period of the 24 h light cycle. The aim of the present study was to determine whether central AT 1 receptor stimulation and the associated ROS signaling contribute to hypertension in BPH/2J mice in a circadian dependent manner. Methods: Blood pressure (BP) was measured in BPH/2J and normotensive BPN/3J mice ( n = 7–8) via pre-implanted telemetry devices. Acute intracerebroventricular (ICV) microinjections of AT 1 receptor antagonist, candesartan, and the superoxide dismutase (SOD) mimetic, tempol, were administered during the dark and light period of the 24 h light cycle via a pre-implanted ICV guide cannula. In separate mice, the BP effect of ICV infusion of the AT 1 receptor antagonist losartan for 7 days was compared with subcutaneous infusion to determine the contribution of the central RAS to hypertension in BPH/2J mice. Results: Candesartan administered ICV during the dark period induced depressor responses which were 40% smaller in BPH/2J than BPN/3J mice ( P strain 1 receptor stimulation may contribute less to BP maintenance in BPH/2J mice. During the light period candesartan had minimal effect on BP in either strain. ICV tempol had comparable effects on BP between strains during the light and dark period ( P strain > 0.08), suggesting ROS signaling is also not contributing to the hypertension in BPH/2J mice. Chronic ICV administration of losartan (22 nmol/h) had minimal effect on BPN/3J mice. By contrast in BPH/2J mice, both ICV and subcutaneously administered losartan induced similar hypotensive responses (−12.1 ± 1.8 vs. −14.7 ± 1.8 mmHg, P route = 0.3 0.31). Conclusion: While central effects of peripheral losartan cannot be excluded, we suggest the hypotensive effect of chronic ICV losartan was likely peripherally mediated. Thus, based on both acute and chronic AT 1 receptor inhibition and acute ROS inhibition, our findings suggest that greater activation of central AT 1 receptors or ROS are unlikely to be mediating the hypertension in BPH/2J mice.


  • 주제어

    renin angiotensin system .   angiotensin II .   neurogenic hypertension .   BPH/2J mice .   central nervous system .   reactive oxygen species.  

 활용도 분석

  • 상세보기

    amChart 영역
  • 원문보기

    amChart 영역

원문보기

유료다운로드
  • 원문이 없습니다.

유료 다운로드의 경우 해당 사이트의 정책에 따라 신규 회원가입, 로그인, 유료 구매 등이 필요할 수 있습니다. 해당 사이트에서 발생하는 귀하의 모든 정보활동은 NDSL의 서비스 정책과 무관합니다.

원문복사신청을 하시면, 일부 해외 인쇄학술지의 경우 외국학술지지원센터(FRIC)에서
무료 원문복사 서비스를 제공합니다.

NDSL에서는 해당 원문을 복사서비스하고 있습니다. 위의 원문복사신청 또는 장바구니 담기를 통하여 원문복사서비스 이용이 가능합니다.

이 논문과 함께 출판된 논문 + 더보기