A. C. Pessina
University of Brescia
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Featured researches published by A. C. Pessina.
Arteriosclerosis, Thrombosis, and Vascular Biology | 2000
Gian Paolo Rossi; Alfredo Sacchetto; Damiano Rizzoni; Sergio Bova; Enzo Porteri; Giuseppina Mazzocchi; Anna S. Belloni; Meltem Bahcelioglu; Gastone G. Nussdorfer; A. C. Pessina
We investigated the role of angiotensin II (Ang II) and endothelin-1 (ET-1) in transgenic (mREN2)27 rats, a model of the monogenic renin-dependent form of severe hypertension and cardiovascular disease. Four-week-old heterozygous male transgenic (mREN2)27 rats (n=24) were matched according to body weight (BW) and blood pressure (BP) and randomly allocated to receive a placebo (group P), the mixed endothelin type A and B receptor antagonist bosentan (100 mg/kg BW PO, group B), the Ang II type 1-specific receptor antagonist irbesartan (50 mg/kg BW PO, group I), or the endothelin type A-selective antagonist BMS-182874 (52 mg/kg BW PO, group BMS). After 4 weeks of treatment, during which BW and BP were measured weekly, animals were euthanized, and the heart, left ventricle, right ventricle, adrenal gland, brain, and kidney were weighed. The plasma levels of adrenocortical steroids were measured by high-performance liquid chromatography. The tension responses of ET-free segments of the thoracic aorta to 5 x 10(-6) mmol/L phenylephrine, 60 mmol/L KCl, and cumulative doses of ET-1 were assessed. The density of ET-1 receptor subtypes in the aorta and vascular structural changes in the mesenteric arterioles (100 to 200 microm ID) were also measured with autoradiography and myography, respectively. Compared with all other groups, group I rats showed significantly (P<0.001) lower systolic BP (group I, 161+/-8 mm Hg; group P, 269+/-23 mm Hg; group B, 275+/-17 mm Hg; and group BMS, 254+/-21 mm Hg), left ventricular weight (2.28+/-0.15 versus 3. 71+/-0.26, 3.38+/-0.27, and 3.96+/-0.51 mg/g BW, respectively), tension responses to vasoconstrictors, and normalized media thickness of the mesenteric arterioles (22.3+/-0.6 versus 25.3+/-0.5, 25.5+/-0.7, and 24.1+/-1.5 microm, respectively). Compared with levels in group P (78+/-25 pmol/mL), plasma aldosterone levels were significantly decreased in group B (51+/-11 pmol/mL) and group I (40+/-16 pmol/mL). Thus, endogenous ET-1 and Ang II contribute to the regulation of aldosterone, but only Ang II is crucial for the development of hypertension and related target organ damage via the Ang II type 1 receptor. Endogenous Ang II does not appear to enhance cardiovascular production of ET-1 in this model of hypertension within the time span of our experiment.
Journal of Internal Medicine | 2006
Maurizio Cesari; A. C. Pessina; Mario Zanchetta; R. De Toni; Angelo Avogaro; Luigi Pedon; Francesca Dorigatti; Giuseppe Maiolino; G.P. Rossi
Objective. To investigate the association of plasma adiponectin levels with coronary artery disease (CAD), arterial hypertension (HT), and insulin resistance (IR) in nondiabetic Caucasian patients.
Journal of Human Hypertension | 2012
Gp Rossi; Tm Seccia; Diego Miotto; P Zucchetta; Diego Cecchin; Lorenzo Calo; Massimo Puato; Raffaella Motta; Paola Caielli; M Vincenzi; G Ramondo; S. Taddei; Claudio Ferri; Claudio Letizia; C Borghi; A Morganti; A. C. Pessina
It is unclear whether revascularization of renal artery stenosis (RAS) by means of percutaneous renal angioplasty and stenting (PTRAS) is advantageous over optimal medical therapy. Hence, we designed a randomized clinical trial based on an optimized patient selection strategy and hard experimental endpoints. Primary objective of this study is to determine whether PTRAS is superior or equivalent to optimal medical treatment for preserving glomerular filtration rate (GFR) in the ischemic kidney as assessed by 99mTcDTPA sequential renal scintiscan. Secondary objectives of this study are to establish whether the two treatments are equivalent in lowering blood pressure, preserving overall renal function and regressing target organ damage, preventing cardiovascular events and improving quality of life. The study is designed as a prospective multicentre randomized, un-blinded two-arm study. Eligible patients will have clinical and angio–CT evidence of RAS. Inclusion criteria is RAS affecting the main renal artery or its major branches either >70% or, if <70, with post-stenotic dilatation. Renal function will be assessed with 99mTc-DTPA renal scintigraphy. Patients will be randomized to either arms considering both resistance index value in the ischemic kidney and the presence of unilateral/bilateral stenosis. Primary experimental endpoint will be the GFR of the ischemic kidney, assessed as quantitative variable by 99TcDTPA, and the loss of ischemic kidney defined as a categorical variable.
Journal of Hypertension | 2013
A. C. Pessina; Bisogni; Ambrogio Fassina; G.P. Rossi
Case report: A young patient presented with a history of resistant arterial hypertension, associated with disabling symptoms. He was subjected to an enormous number of tests to identify a pheochromocytoma that was never found. He was eventually discovered to make factitious use of amphetamine to mimic this condition in order to gain medical attention. Munchausen syndrome was thus diagnosed. The patient was discharged and was lost to follow-up until he presented again in 2012 for ‘resistant hypertension’ in our outpatient clinic. He reported that because of poor blood pressure, he had been referred to a Cardiology department where transcatheter renal denervation was performed with no effect on blood pressure. Thereafter, he was presented to an Endocrinology unit where a left adrenalectomy was performed with diagnosis of pheochromocytoma that was not found at pathology. Discussion: Munchausen syndrome is a rare psychiatric condition that leads affected patients to cause intentionally signs and symptoms of an illness or injury by inflicting medical harm to their body to attract the attention of the physician and get admission to the hospital. Conclusion: To our knowledge, this is the first case of causing drug-resistant hypertension and leading to unnecessary renal denervation and adrenalectomy.
The American Journal of Medicine | 1992
Ettore Ambrosioni; Giorgio Finardi; Pietro Folino; Gino Gambassi; Pierluigi Malini; Eugenia Marchesi; Maria Lorenza Muiesan; Andrea Semplicini; A. C. Pessina
The aim of this 3-month, double-blind, double-dummy, parallel group study was to compare the antihypertensive efficacy and acceptability of perindopril (4-8 mg/day) in 54 patients (30 males, 24 females, 25-68 years of age) and captopril (50-100 mg/day) in 54 patients (39 males, 15 females, 29-66 years of age) in the treatment of essential hypertension. In a subgroup of 38 patients a complete echocardiographic study was performed. The two groups had similar (ANOVA) blood pressure (BP), heart rate (HR), body mass index, and duration of hypertension. Supine and standing BP was significantly reduced by both drugs, without differences between them. Owing to poor control of BP, hydrochlorothiazide (25 mg/day) was added to 27% of patients on perindopril and to 41% of patients on captopril (p less than 0.05). Normalization of supine diastolic BP (less than or equal to 90 mm Hg) was obtained in 67% of patients on perindopril and in 47% of patients on captopril (p less than 0.01). No change in HR was detected. Only mild untoward effects were recorded. Left ventricular mass was significantly reduced by either drug, with no change in systolic function. In conclusion, perindopril and captopril, at these doses, were both well tolerated and on average reduced BP to a similar extent; however, treatment with perindopril showed that fewer patients needed the addition of a thiazide and BP became normal in a larger number of patients.
Hypertension | 2018
Gian Paolo Rossi; Giuseppe Maiolino; Alberto Flego; Anna Belfiore; Giampaolo Bernini; Bruno Fabris; Claudio Ferri; G. Giacchetti; Claudio Letizia; M Maccario; Francesca Mallamaci; Maria Lorenza Muiesan; Massimo Mannelli; Aurelio Negro; Gaetana Palumbo; Gabriele Parenti; Ermanno Rossi; Franco Mantero; Andrea Semplicini; Chiara Ganzaroli; A. C. Pessina; Vanessa Ronconi; Marco Boscaro; Angelica Moretti; Giovambattista Desideri; G. Andronico; Damiano Rizzoni; Enzo Porteri; Chiara Caliumi; Ezio Ghigo
Current Medicinal Chemistry - Cardiovascular & Hematological Agents | 2005
Maurizio Cesari; Gian Paolo Rossi; A. C. Pessina
Journal of Hypertension | 2011
Tm Seccia; Diego Miotto; R. De Toni; V. Gallina; A. C. Pessina; G.P. Rossi
Journal of Hypertension | 2011
G.P. Rossi; Gisella Pitter; V. Gallina; Giacomo Rossitto; A. C. Pessina
Journal of Hypertension | 2011
C Recarti; Tm Seccia; Livia Lenzini; Ghizlane Skander; Brasilina Caroccia; Giulio Ceolotto; Lucia Petrelli; Anna S. Belloni; A. C. Pessina; G.P. Rossi