Professor of Internal Medicine,
Roy J. Carver Chair in Hypertension Research
The mechanism controlling cell-specific Ang-II production in the brain remains unclear despite evidence supporting neuron-specific
reninand glial- and neuronal-specific angiotensinogen expression. We generated double transgenic mice (termed SRA) expressing
human renin (hREN) rom a neuron-specific promoter and human angiotensinogen (hAGT) from its own promoter to emulate this
expression. SRA mice exhibited an increase in water and salt intake and urinary volume which was significantly reduced after chronic
intracerebroventricular delivery of Losartan. Ang-II-like immunoreactivity was markedly increased in the subfornical organ (SFO).
To further evaluate the physiological importance of de novo Ang-II production specifically in the SFO, we utilized a transgenic mouse model
expressing a "floxed" version of hAGTflox so deletions could be induced with Cre-recombinase. We targeted SFO-
specific ablation of hAGTflox by microinjection of an adenovirus encoding Cre-recombinase AdCre). SRA
flox mice exhibited a marked increase in drinking at baseline and a significant decrease in water intake after
AdCre/AdeGFP, but not after AdeGFP alone. This decrease only occurred when Cre-recombinase correctly targeted
the SFO and correlated with a loss of hAGT and angiotensin peptide immunostaining in the SFO. These data provide strong genetic evidence
implicating de novo synthesis of Ang-II in the SFO as an integral player in fluid homeostasis. The results of this study published in the Journal of Clinical Investigation (117:1088-1095, 2007) was the topic of an editorial in the journal and illustrates how we use a combination of high tech genetics, genetic techniques and integrative physiology to make fundamental discoveries on the neural control of blood pressure regulation.
Sigmund named to Carver Chair in Hypertension Research
Curt D. Sigmund, Ph.D., professor of internal medicine and molecular physiology and biophysics in the UI Roy J. and Lucille A. Carver College of Medicine, has been named to the Roy J. Carver Chair in Hypertension Research. The five-year appointment was effective July 1.
http://news-releases.uiowa.edu/2008/july/070208sigmund-carverchair.html
Selected Publications
Halabi, C.M., Beyer, A.M., de Lange, W.J., Keen H.L. Faraci, F.M. and Sigmund, C.D. Interference with PPARy Function in Smooth Muscle Causes Vascular Dysfunction and Hypertension. Cell Metabolos. 7, 215-226, 2008.
Beyer, A.M., Baumbach, G.L.., Halabi, C.M., Modrick, M.L.., Lynch, C.M., Gerhold, T.D., Ghomeim, S.M., deLande, W.J., Keen, H.L., Tsai, Y-S., Maeda, N., Sigmund, C.D., and Faraci, F.M., Interference with PPARy Signaling Causes Cerebral Vascular Dysfuntion, Hypertrophy, and Remodeling.Hypertension 51: 867-871, 2008.
Sakai, K., Agassandian, K., Morimoto, S., Sinnayah, P., Cassell, M.D., Davisson, R.L. and Sigmund, C.D. Local Productio of Angiotensin-ll in the Subfornical Organ Causes Elevated Drinking. J Clinical Investigation 117, 1088-1095, 2007.
Dickson, M.E., Zimmerman, M.B., Rahmouni, K., and Sigmund, C.D. The -20 and -217 Promoter Variants Dominate Differential Angiotensinogen Haplotype Regulation in Angiotensinogen-Expressing Cells. Hypertension 49 631-639, 2007.
Itani, H.A., Liu X., Pratt, J.H. and Sigmund, C.D. Functional Characterization of Polymorphisms in the Kidney Enhancer of the Human Renin Gene. Endocrinology 148 1424-1430, 2007.