Modulation of contractility by myocyte-derived arginase in normal and hypertrophied feline myocardium
| Autor: | Hajime Kubo, Kenneth B. Margulies, Rachel M Wilson, Albert S. Jung, Steven R. Houser |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
medicine.medical_specialty
Physiology chemistry.chemical_element Calcium Biology In Vitro Techniques Nitric Oxide Nitric oxide Muscle hypertrophy Contractility chemistry.chemical_compound Physiology (medical) Internal medicine medicine Myocyte Animals Humans Cells Cultured Muscle Cells ATP synthase Arginase Substrate (chemistry) Myocardial Contraction Endocrinology chemistry biology.protein Cats Hypertrophy Left Ventricular Cardiology and Cardiovascular Medicine |
| Zdroj: | American journal of physiology. Heart and circulatory physiology. 290(5) |
| ISSN: | 0363-6135 |
| Popis: | l-Arginine, the sole substrate for the nitric oxide (NO) synthase (NOS) enzyme in producing NO, is also a substrate for arginase. We examined normal feline hearts and hearts with compensated left ventricular (LV) hypertrophy (LVH) produced by ascending aorta banding. Using Western blot analysis, we examined the abundance of arginase isozymes in crude homogenates and isolated cardiac myocytes obtained from the LVs of normal and LVH hearts. We examined the functional significance of myocyte arginase via measurement of shortening and intracellular calcium in isolated myocytes in the presence and absence of boronoethyl chloride (BEC), a specific pharmacological inhibitor of arginase. Both arginase I and II were detected in crude myocardial homogenates, but only arginase I was present in isolated cardiac myocytes. Arginase I was downregulated in LVH compared with normal. Inhibition of arginase with BEC reduced fractional shortening, maximal rate of shortening (+d L/d t) and relengthening (−d L/d t), and the peak of the free cytosolic calcium transient in normal myocytes but did not affect these parameters in LVH myocytes. These negative inotropic actions of arginase inhibition were associated with increases in cGMP generation. These studies indicate that only arginase I is present in cardiac myocytes where it tends to limit NO and cGMP production with the effect of supporting basal contractility. In experimental LVH induced by pressure overload, our studies demonstrate reduced arginase I expression and reduced functional significance, allowing greater arginine substrate availability for NO/cGMP signaling. |
| Databáze: | OpenAIRE |
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