Another possibility is definitely that growth responses via Ang IICAT1R are mediated in part by ERK1/2 MAP kinases, JNK and Akt, while its pro-fibrotic actions are mediated through TGF- dependent signaling cascades . (decreased tightness). Losartan treatment decreased wall thickness, wall-to-lumen percentage, and coronary arteriole cell number in db/db mice. Losartan treatment did not impact incremental elastic modulus. However, losartan improved coronary circulation reserve. Our data suggest that Ang IICAT1R signaling mediates, at least in part, coronary arteriole inward hypertrophic redesigning in T2DM without influencing vascular mechanics, further suggesting that focusing on the coronary microvasculature in T2DM may help reduce cardiac ischemic events. knockout (kindly provided by Dr. LM Harrison-Barnard) to DprE1-IN-2 generate heterozygous db/dbAT1Ra+/? mice and double homozygous (db/dbAT1Ra?/?) mice . Please note that this colony was lost during Hurricane Katrina, avoiding further experimentation. All other experiments were carried out on 12 or 16 week-old male control, non-diabetic heterozygous (Db/db; BKS.Cg-method, with the ribosomal protein transcript Rpl13a offering as the internal control  and the average Het value for the aorta offering as the second normalizer. 2.3. Drug treatment Control or db/db mice were administered vehicle water or losartan (3 mg/kg/day time) (Sigma, 61188), treated water for 4 weeks, beginning at 12 weeks of age. Water bottles were changed 2 times a week. This dose of losartan was chosen based upon a previous statement that doses 10 mg/kg/day time in diabetic mice do not impact blood pressure . 2.4. Blood glucose, insulin and plasma Ang II measurements Prior to end point experiments, fasting blood glucose (8C10 hour food withdrawal during the light cycle) was measured from DprE1-IN-2 tail vein blood using the Accu-Chek Advantage meter (Roche, Indianapolis, Indiana). Insulin levels were measured using an ELISA kit from Mercodia (Winston-Salem, NC). The offered protocol was adopted exactly, with the following exclusion: All db/db samples were diluted 1:3 with Calibrator 0 remedy prior to assay (i.e. 20 L plasma + 40 L Calibrator 0). This was done in anticipation of db/db mouse insulin levels being very high. Samples were read on the SpectraMax M5 spectrophotometer. Plasma Ang II concentrations were measured by radioimmunoassay at Hypertension Core lab at Wake Forest University or college. 2.5. Coronary arteriole isolation and measurement of structural and passive mechanical properties At the end of treatment (16 weeks) mice were anesthetized using 3% isoflurane, vaporized with 100% oxygen. The heart was excised and dissected in chilly physiologic salt answer (PSS). The right ventricle was removed and septal coronary arterioles ( 120 m internal diameter) at the level of the superior papillary muscle were isolated, excised and mounted onto two glass microcannulas within a pressure myograph chamber (Living Systems, Burlington, VT) as previously explained by our lab . One vessel was isolated ENG per animal. Prior to any measurements, vessels were equilibrated for 30 min under constant intraluminal pressure (50 mm Hg) at 37 C in PSS. Internal diameter and left and right wall thickness (WT) were continuously monitored by a video image analyzer (Living Systems) and recorded using LabCart 6 data acquisition software connected to a PowerLab 16/30 (ADInstruments, Inc., DprE1-IN-2 Colorado Springs, CO). All experiments were performed in Ca2+-free PSS in DprE1-IN-2 the presence of 2 mM EGTA and 100 M sodium nitroprusside. A passive pressureCdiameter curve was generated by increasing intraluminal pressure from 0 to 125 mm Hg. Coronary wall thickness (WT) and internal diameters (Di) were recorded at each pressure. The following structural and mechanical parameters were calculated as previously explained : External diameter (De) = is the internal coronary diameter (in mm) measured in B-mode ultrasound images, VTI is the velocityCtime-integral (in mm), or area under the curve of the Doppler blood flow velocity tracing, and HR is the heart rate. Coronary circulation reserve (CFR) = CBFhyperemia/CBFbaseline where CBFhyperemia is usually coronary flow measured during 3% isoflurane administration. 2.8. Blood pressure telemetry Radiotelemetry transmitters (PA-C10, Data Sciences, St. Paul, MN) were implanted into mice as DprE1-IN-2 explained by our lab . Briefly, mice were anesthetized with 2% isoflurane, and the right carotid artery was isolated and cannulated with a telemeter catheter connected to a radio-telemetry transmitter. Since db/db mice are more sensitive to surgical stressors, data recording commenced after the return of normal diurnal blood pressure rhythms (7C10 days). Data were collected for 10 s every 15 min for a total of 4.