Literature DB >> 19307983

Endothelial damage due to impaired nitric oxide bioavailability triggers cerebral aneurysm formation in female rats.

Tetsuya Tamura1, Mohammad A Jamous, Keiko T Kitazato, Kenji Yagi, Yoshiteru Tada, Masaaki Uno, Shinji Nagahiro.   

Abstract

OBJECTIVE: Epidemiological data indicate a high incidence of cerebral aneurysms in postmenopausal women. To elucidate the pathogenesis of cerebral aneurysms, we focused on the contribution of endothelial damage in rats.
METHODS: We induced estradiol deficiency by oophorectomy (OVX), hypertension, or both, and hemodynamic stress in 7-week-old female Sprague-Dawley rats. They were then given hormone-replacement therapy with 17beta-estradiol or an angiotensin II type 1 receptor blocker (ARB). The effects of estradiol, angiotensin II type 1 receptor blocker, or both on cultured endothelial cells were also examined.
RESULTS: The number of anomalously shaped endothelial cells was higher in OVX than hypertensive rats (P < 0.05). Rats subjected to hypertension and OVX exhibited a marked increase in the incidence of saccular cerebral aneurysms. Estradiol or angiotensin II type 1 receptor blocker treatment reduced this incidence (P < 0.05). The endothelial nitric oxide synthase (eNOS) mRNA level in the intracranial artery of OVX and hypertensive and OVX rats was low (P < 0.05). Immunohistochemically, the expression of eNOS and estrogen receptor alpha (ERalpha) in the vascular wall of hypertensive and OVX rats was decreased; angiotensin II and the nicotinamide adenine dinucleotide phosphate oxidase subunits nicotinamide adenine dinucleotide phosphate oxidase 4 and p22phox were strongly expressed in cerebral aneurysms. In the absence of estradiol, eNOS was downregulated and nicotinamide adenine dinucleotide phosphate oxidase expression was increased in endothelial cells; angiotensin II augmented these phenomena. The regulation of eNOS was mediated by ERalpha. These results suggest that estrogen deficiency induces endothelial dysfunction and reactive oxygen species generation, triggering endothelial damage that leads to cerebral aneurysms and that hypertension is an additional risk factor.
CONCLUSION: A therapy targeted at the endothelium and management of hypertension may help to prevent cerebral aneurysms.

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Year:  2009        PMID: 19307983     DOI: 10.1097/HJH.0b013e328329d1a7

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  27 in total

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3.  Late onset MELAS with m.3243A > G mutation and its association with aneurysm formation.

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Review 4.  Sex differences in vascular physiology and pathophysiology: estrogen and androgen signaling in health and disease.

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Journal:  J Cereb Blood Flow Metab       Date:  2016-01-01       Impact factor: 6.200

Review 6.  Current therapeutic strategies to mitigate the eNOS dysfunction in ischaemic stroke.

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Review 8.  Sex Differences in the Formation of Intracranial Aneurysms and Incidence and Outcome of Subarachnoid Hemorrhage: Review of Experimental and Human Studies.

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Review 9.  The role of oxidative stress in cerebral aneurysm formation and rupture.

Authors:  Robert M Starke; Nohra Chalouhi; Muhammad S Ali; Pascal M Jabbour; Stavropoula I Tjoumakaris; L Fernando Gonzalez; Robert H Rosenwasser; Walter J Koch; Aaron S Dumont
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10.  Estrogen protects against intracranial aneurysm rupture in ovariectomized mice.

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Journal:  Hypertension       Date:  2014-04-14       Impact factor: 10.190

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