Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Vincenzo Panagia"'
Publikováno v:
Molecular and Cellular Biochemistry. 283:93-100
In this study, we examined changes in the biochemical and inotropic events of the alpha(1)-adrenoceptor signaling pathway in hypothyroid rat hearts. Hypothyroidism was induced by treating experimental animals with 0.05% 6-n-propyl-2-thiouracil (PTU)
Autor:
J. Alejandro Austria, Nidhi Sahi, Grant N. Pierce, Thane G. Maddaford, Vincenzo Panagia, Paramjit S. Tappia, Cecilia Hurtado, Elena Dibrov
Publikováno v:
Biochemical and Biophysical Research Communications. 316:280-289
The effects of exogenous phosphatidic acid (PA) on Ca2+ transients and contractile activity were studied in cardiomyocytes isolated from chronic streptozotocin-induced diabetic rats. In control cells, 25 μM PA induced a significant increase in activ
Autor:
Chang-Hua Yu, Vincenzo Panagia, Naranjan S. Dhalla, Paramjit S. Tappia, Song-Yan Liu, Nobuakira Takeda
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1584:65-72
Phospholipase D 2 (PLD2) is the major PLD isozyme associated with the cardiac sarcolemmal (SL) membrane. Hydrolysis of SL phosphatidylcholine (PC) by PLD2 produces phosphatidic acid (PA), which is then converted to 1,2 diacylglycerol (DAG) by the act
Autor:
Paramjit S. Tappia, Naranjan S. Dhalla, Paolo Di Nardo, Chang-Hua Yu, Vincenzo Panagia, Ajai K. Pasricha
Publikováno v:
Journal of Molecular and Cellular Cardiology. 33:431-440
The cardiac sarcolemmal membrane cis -unsaturated fatty acid-sensitive phospholipase D hydrolyzes phosphatidylcholine to form phosphatidic acid. The functional significance of phosphatidic acid is indicated by its ability to increase [Ca 2+ ] i and a
Autor:
Attila Ziegelhoffer, Vincenzo Panagia, Nidhi Sahi, Nasrin Mesaeli, Naranjan S. Dhalla, Paramjit S. Tappia
Publikováno v:
Cardiovascular Research. 49:118-126
Objective: Phosphatidylinositol 4,5-bisphosphate (PtdIns 4,5-P2) is not only a precursor to inositol 1,4,5-trisphosphate (Ins 1,4,5-P3) and sn -1,2 diacylglycerol, but also essential for the function of several membrane proteins. The aim of this stud
Autor:
Paramjit S. Tappia, Mohinder S. Nijjar, Kenichi Kawabata, Naranjan S. Dhalla, Kanhaiya R. Shah, Vincenzo Panagia, Kenji Okumura
Publikováno v:
Molecular and Cellular Biochemistry. 221:89-98
Evidence indicates that, in addition to the L-type Ca2+ channel blockade, Ca2+-antagonists target other functions including the Ca2+-pumps. This study was conducted to test the possibility that the reported inhibition of heart sarcolemmal (SL) and sa
Publikováno v:
Europe PubMed Central
Cardiac sarcolemmal Na+/H+exchange is critical for the regulation of intracellular pH, and its activity contributes to ischemia-reperfusion injury. It has been suggested that the membrane phospholipid environment does not modulate Na+/H+exchange. The
Heart Hypertrophy and Failure brings together leading basic scientists and clinicians, presenting improved knowledge of the pathophysiology and treatment of the condition. The result is a synthesis of state-of-the-art information on molecular biology
Publikováno v:
Journal of Cardiovascular Pharmacology and Therapeutics. 3:239-245
Background: Some β-adrenoceptor antagonists exert a negative inotropic action by affect ing Ca2+ fluxes in the myocardial cell as a consequence of their interaction with sarcolem mal and sarcoplasmic reticular membranes. This action may be caused by