Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P50502 (
Hip
)
7,003
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Angiotensin-converting enzyme (ACE) was studied in preparations of microvessels isolated from rabbit cerebral cortex. Activity was determined by measuring the degradation of hippuryl-histidyl-leucine (Hip-His-Leu) by the intact microvessels in a physiological salt solution at pH 7.4. ACE activity was dependent on both substrate and chloride ion concentration and was inhibited by captopril in a manner similar to that observed previously with tissue homogenates. Angiotensin I was rapidly degraded by the intact microvessels, even in the presence of 10(-6)M captopril. An advantage of the methodology employed was the ability to pretreat the microvessels and then assess the effect of pretreatment by transfer to a postincubation assay system. Pretreatment with a hyperosmolar
urea
solution did not change ACE activity or cause release of ACE from the microvessels, although lactic dehydrogenase and lysosomal enzymes were released. Pretreatment with captopril caused a lag in the subsequent degradation of
Hip
-His-Leu, presumably reflecting dissociation of inhibitor from the cell-associated enzyme. ACE activity was unaffected by hypoxic or anoxic incubation conditions. The ability to measure ACE activity of the microvessels in vitro provides a unique opportunity to study the properties of the enzyme in intact cerebrovascular endothelial cells.
...
PMID:Properties of angiotensin-converting enzyme in intact cerebral microvessels. 626 Jun 46
Sixty Holstein heifers, 124.5 +/- 1.1 d of age and 124.9 +/- 2.5 kg of BW, were used to evaluate the influence of dietary crude protein to metabolizable energy ratio (CP:ME) on feed efficiency, structural growth, and body condition score. Treatment rations containing a specific CP:ME ratio were assigned to heifers in a complete randomized block design with treatment periods lasting 20 wk. The CP:ME ratios were 48.3, 59.1, 67.5, and 76.5 g of CP per Mcal of ME. The CP:ME ratios were altered by adjusting the concentration of CP (12.0,15.2, 17.4, and 19.7% CP) with similar amounts of ME (2.6 Mcal/kg DM) across all treatment rations. BW was recorded weekly on two consecutive days and used to adjust dry matter intake to allow approximately 0.80 kg/d gain. Average daily gain did not differ between the treatment rations, 0.74, 0.81, 0.81, 0.77 kg/d, low to highest CP:ME ratio, respectively. Dry matter intake showed a quadratic effect for the treatment rations, 3.30, 3.41, 3.48, and 3.39 kg/d, low to highest CP:ME ratio, respectively, and averaged 2.0% BW. Feed efficiency improved linearly with increasing CP:ME ratios, 4.76, 4.42, 4.35, and 4.33, respectively. The increased CP:ME ratios were accompanied by increasing levels of plasma
urea
N, 9.88, 13.34, 14.94, and 16.57 mg/dl, respectively. A trend toward linear increases in wither and hip height growth resulted with increasing CP:ME.
Hip
width growth was quadratic with increasing CP:ME ratios. Observed linear effects in feed efficiency and some structural growth measurements demonstrate positive results when feeding CP:ME ratios >48.3 to Holstein heifers between 125 and 234 kg of BW and gaining 0.80 kg/d.
...
PMID:Dietary protein to metabolizable energy ratios on feed efficiency and structural growth of prepubertal Holstein heifers. 1261 70