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          Institute: MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut)     Collection: Publikationen des W. G. Kerckhoff-Instituts     Display Documents

ID: 313324.0, MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut) / Publikationen des W. G. Kerckhoff-Instituts
Neurogenic mechanisms contribute to hypertension in mice with disruption of the K-Cl cotransporter KCC3
Authors:Rust, M. B.; Faulhaber, J.; Budack, M. K.; Pfeffer, C.; Maritzen, T.; Didie, M.; Beck, F. X.; Boettger, T.; Schubert, R.; Ehmke, H.; Jentsch, T. J.; Hubner, C. A.
Date of Publication (YYYY-MM-DD):2006-03-03
Title of Journal:Circ Res
Journal Abbrev.:Circ Res
Issue / Number:4
Start Page:549
End Page:556
Audience:Not Specified
Abstract / Description:The neurodegenerative disorder Andermann syndrome is caused by mutations of the K-Cl cotransporter KCC3. Mice with a targeted disruption of the corresponding gene, Slc12a6, reproduce neurodegeneration of the peripheral and central nervous system (CNS) and display arterial hypertension. Kcc3 is expressed in numerous tissues, including the CNS and vascular smooth muscle cells. As the intracellular chloride concentration may influence myogenic tone and hence blood pressure, we measured the chloride concentration in vascular smooth muscle cells. It was indeed increased in superficial brain arteries and saphenous arteries of Kcc3(-/-) mice. Isolated saphenous arteries and their third-order branches, however, reacted indistinguishably to changes in intravascular pressure, stimulation of alpha1-adrenoreceptors, exogenous nitric oxide, or blockade of calcium-activated chloride channels. Likewise, the responses to alpha1-adrenergic stimulation or exogenous nitric oxide in vivo were identical in both genotypes. These results argue against a major vascular-intrinsic component of arterial hypertension in Kcc3(-/-) mice. In contrast, either alpha1-adrenergic blockade or inhibition of ganglionic transmission abolished the difference in arterial blood pressure between both genotypes. This demonstrates a neurogenic component in the maintenance of this phenotype, which is further supported by an increase of urinary norepinephrine and epinephrine excretion in Kcc3(-/-) mice. Our data indicate that local control of myogenic tone does not require KCC3 and that hypertension in Kcc3(-/-) mice depends on an elevated sympathetic tone.
Free Keywords:Aldosterone/blood Animals Calcium/metabolism Chlorides/metabolism Hypertension/*etiology/physiopathology Mice Mice, Inbred C57BL Mice, Knockout Muscle, Smooth, Vascular/metabolism Renin-Angiotensin System/physiology Sympathetic Nervous System/*physiology Symporters/*physiology Vasoconstriction
External Publication Status:published
Document Type:Article
Communicated by:N. N.
Affiliations:MPI für physiologische und klinische Forschung
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