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Dive into the research topics where Alessandro Perrone is active.

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Featured researches published by Alessandro Perrone.


Gastroenterology | 1995

Peripheral monocyte and naive T-cell recruitment and activation in Crohn's disease

Vito L. Burgio; Stefano Fais; Monica Boirivant; Alessandro Perrone; Francesco Pallone

BACKGROUND & AIMS Transmural perivascular mononuclear cell infiltrates are a feature of Crohns disease. The aim of this study was a molecular characterization of the mechanisms leading to the formation of these infiltrates. METHODS Endothelial cell and leukocyte expression of the adhesion molecules directing leukocyte transendothelial migration were studied in situ by immunohistochemical analysis of 10 samples from patients with Crohns disease and 10 samples from normal controls. Double-staining methods were used to characterize the cells forming the infiltrates. RESULTS CD11a+ and L-selectin-positive mononuclear cells seemed to be the major component of perivascular infiltrates. The vast majority of these cells were CD68+, CD31+ monocytes/macrophages surrounded by CD3+, L-selectin-positive, CD31+, CD45RA+, and/or CD45RO+ T lymphocytes. T lymphocytes within the vessels expressed both CD45RA and CD45RO markers. Endothelial cells were intercellular adhesion molecule 1 positive and mostly CD34+. Strong adhesion between L-selectin-positive and CD11a+ intravascular mononuclear cells and CD34+ and intercellular adhesion molecule 1-positive endothelial cells were observed. CONCLUSIONS Data indicate that peripheral mononuclear cells are actively recruited in the submucosa of Crohns disease tissue; endothelial cells express adhesion molecules highly permissive for transendothelial migration of monocytes and both naive and memory T cells contributing to infiltrates generation; and close membrane contact between migrated macrophages and naive T cells leads to the T-cell transition from naive to memory phenotype within Crohns disease.


Journal of Clinical Pathology | 1995

Circulating endothelin-1 concentrations in patients with chronic hypoxia.

Claudio Ferri; C. Bellini; C De Angelis; L De Siati; Alessandro Perrone; G Properzi; A. Santucci

AIMS--To evaluate the behavior of plasma endothelin-1 in patients with chronic hypoxia. METHODS--Fifteen male patients (mean age 52.1 +/- 3.1 years) with mild chronic obstructive pulmonary disease (COPD) were studied. Twelve healthy men (mean age 48.3 +/- 5.4 years) served as controls. Both patients and controls underwent standard pulmonary function tests, echocardiographic evaluation, and arterial blood gas evaluation. Blood samples for endothelin-1 assay were taken from a previously incannulated antecubital vein after 60 minutes of rest in the supine position. Endothelin-1 was measured by radioimmunoassay after extraction from plasma. RESULTS--Patients with chronic hypoxia had lower PaO2 values (66.1 +/- 6.2 mmHg) than controls (83.8 +/- 2.7 mmHg) but PaCO2 values were similar (38.1 +/- 2.5 v 36.7 +/- 3.1 mmHg, respectively). Arterial pulmonary pressure, therefore, was higher in patients (18.1 +/- 3.7 mmHg) than in controls (10.4 +/- 2.7 mmHg) as were circulating endothelin-1 concentrations (1.22 +/- 0.36 v 0.57 +/- 0.1 pg/ml). Furthermore, plasma endothelin-1 concentrations were negatively correlated with PaO2 and directly correlated with pulmonary pressure levels. No significant correlations were found in controls. CONCLUSIONS--These results show a clear relation between chronic hypoxia and circulating endothelin-1 concentrations. Therefore, chronic hypoxia may be regarded as an important stimulus for endothelin-1 release and as one of the main contributors to increased vasoconstriction in the vascular pulmonary bed which often accompanies lung disease.


Circulation | 1994

Abnormal atrial natriuretic peptide and renal responses to saline infusion in nonmodulating essential hypertensive patients.

Claudio Ferri; Cesare Bellini; Simonetta Coassin; Roberta Baldoncini; Riccardo Leonetti Luparini; Alessandro Perrone; Anna Santucci

BackgroundNonmodulation seems to represent an inheritable trait characterized by abnormal angiotensin-mediated control of aldosterone release and renal blood supply and salt-sensitive hypertension. Recently, we demonstrated that atrial natriuretic peptide (ANP) response to angiotensin II also is altered in nonmodulators. Moreover, an abnormal ANP response to acute volume expansion has been shown by others in hypertensive patients displaying some features of nonmodulators. These data induced us to hypothesize that nonmodulators. These data induced us to hypothesize that nonmodulation could be characterized by an abnormal ANP response to saline load. Methods and ResultsForty-three essential hypertensive men were subdivided into low-renin patients (n = 12), nonmodulators (n = 15), and modulators (n = 16) according to their renin profile and ability to modulate aldosterone and p-aminohippurate clearance responses to a graded angiotensin II infusion (1.0 ng.kg-1·min−1 and 3.0 ng·kg−1.min−1 for 30 minutes each) on both a low- (10 mmol Na+ per day) and a high- (210 mmol Na+ per day) Na+ intake. The intravenous saline load (0.25 mL.kg−1−min−1 for 2 hours) performed on a low-Na+ diet increased plasma ANP levels in low-renin (from 14.30 ± 4.68 to 23.30 ± 7.52 fmol/mL at 120 minutes, P < .05) and modulating patients (from 10.95 ± 3.55 to 18.21 ± 5.42 fmol/mL at 120 minutes, P < .05), whereas it did not change the hormone levels in nonmodulators (from 10.77 ± 3.25 to 13.83 ± 5.70 fmol/mL at 120 minutes, P = NS). When patients switched from a low- to a high-NaCl diet, plasma ANP levels increased significantly in all groups. However, when the saline load was repeated on a high-NaCl intake, ANP levels increased in both low-renin and modulating patients (P < .05), whereas it failed to increase in nonmodulators. ConclusionsNonmodulating hypertensive patients showed a reduced ANP response to saline infusion in the presence of a normal increase of plasma ANP with dietary NaCl load. The impaired ANP response to saline infusion could be due to a different distribution of volume load and contribute to determining the reduced ability to excrete sodium that is commonly described in nonmodulators.


American Journal of Nephrology | 1993

Oxygen Administration Increases Plasma Digoxin-Like Substance and Renal Sodium Excretion in Chronic Hypoxic Patients

Claudio De Angelis; Alessandro Perrone; Claudio Ferri; Alfonso Piccoli; Cesare Bellini; Raffaele D’Amelio; Anna Santucci; F. Balsano

Despite the absence of cardiac or renal pathologies, edema and mild hyponatremia may often occur in patients affected by chronic obstructive pulmonary disease (COPD). Therefore, it has been suggested that hypoxia may influence the release of different hormones regulating renal sodium handling. To evaluate the effect of hyperoxia and O2 removal on plasma digitalis-like substance (DLS) levels, 9 patients affected by COPD and 7 normal subjects were studied. After 1 h in supine position, O2 was administered for 3 h by a tight-fitting face-mask. Blood samples for plasma DLS were taken at time 0, 60, 180 min and then for 3 h after O2 removal. In normal subjects, plasma DLS did not vary after O2 administration (from basal values of 162.25 +/- 8.59 to 107.75 +/- 6.65 pg/ml at 180 min; NS), and O2 removal (143.7 +/- 16.87 pg/ml after 3 h from O2 removal; NS). On the contrary, in patients affected by COPD, plasma DLS levels increased during O2 administration (from basal values of 138.98 +/- 8.31 to 202.14 +/- 8.21 pg/ml at 180 min; p < 0.05), and returned to baseline levels (142.59 +/- 8.28 pg/ml) 3 h after O2 removal. In the same patients, DLS increase was accompanied by a rise in Na+ excretion (from 0.08 +/- 0.01 at time 0 to 0.16 +/- 0.02 mEq/min after 3 h of O2 administration; p < 0.05). In conclusion, our findings showed an oxygen-related increase in plasma DLS levels and in urinary Na+ excretion in patients affected by COPD. This phenomenon could promote Na+ urinary loss during prolonged O2 therapy in these patients and should be taken into account in their management.


International Journal of Cardiology | 1992

Enhanced release of atrial natriuretic factor during exercise-induced myocardial ischaemia in patients after acute myocardial infarction

Paolo De Marzio; Sergio Morelli; Claudio Ferri; Giuseppina Torregrossa; Cesare Bellini; Claudio De Angelis; Alessandro Perrone; Francesco Aguglia; Anna Santucci; F. Balsano

To determine whether acute myocardial ischaemia induced by dynamic exercise can lead to changes in plasma levels of atrial natriuretic factor, we performed symptom-limited bicycle electrocardiographic tests in 20 males with recent acute myocardial infarction and in 8 control males. Ten patients developed exercise-induced myocardial ischaemia and 10 patients did not. There were no significant differences between the two groups with regard to age, site of myocardial infarction, urinary sodium, atrial sizes, radionuclide left ventricular ejection fraction, workload, baseline and peak-exercise heart rate, baseline and peak-exercise rate-pressure product, duration of exercise. Also baseline atrial natriuretic factor concentrations were similar in both groups (ischaemic patients: 34.51 +/- 15.73 pg/ml; nonischaemic patients: 27.17 +/- 8.74 pg/ml, NS), while peak-exercise atrial natriuretic factor concentrations were higher in patients with exercise-induced myocardial ischaemia (112.31 +/- 35.5 pg/ml) than in the others (80.46 +/- 23.43 pg/ml) (P less than 0.05). After 15 minutes of recovery, plasma atrial natriuretic factor levels were still raised only in the ischaemic patients (63.3 +/- 15.44 pg/ml, P less than 0.01), returning to baseline after 30 minutes in both groups. In control subjects, the behaviour of atrial natriuretic factor resembled that of the patients without exercise-induced ischaemia, with a significant increase at peak-exercise (from baseline levels of 23.1 +/- 10.5 pg/ml to peak-exercise levels of 91.3 +/- 14.5 pg/ml, P less than 0.0005) and a rapid return to baseline levels after 15 minutes of recovery (28.5 +/- 10.6 pg/ml, NS).(ABSTRACT TRUNCATED AT 250 WORDS)


Respiration | 1993

Renal Sodium Excretory Function during Acute Oxygen Administration

Luca De Siati; Roberta Baldoncini; Simonetta Coassin; Claudio De Angelis; Claudio Ferri; Anna Santucci; Alessandro Perrone; F. Balsano

To evaluate the effect of O2 administration and O2 removal on renal Na+ excretion, 12 hypoxemic eucapnic patients affected by chronic obstructive pulmonary disease (COPD) and 9 normal subjects were studied. After 1 h in the supine position, O2 was administered for 3 h by a tight-fitting face-mask. Urine and blood samples for renal Na+ excretion evaluation were taken at times 0, 60 and 180 min. After O2 removal both the blood and the urine samples were taken again for a further 3 h. In normal subjects, urinary Na+ excretion did not vary after both O2 administration and removal. On the contrary, in patients affected by COPD renal Na+ excretion significantly increased during O2 administration (from basal values of 0.08 +/- 0.01 to 0.17 +/- 0.02 mEq/min at 180 min, p < 0.05), and returned to baseline levels (0.13 +/- 0.03 mEq/min) after 3 h from O2 removal. The basal fractional excretion of filtered Na+ was significant lower in hypoxemic patients than in normal subjects (0.72 +/- 0.3% in patients with COPD vs. 0.95 +/- 0.7% in normal subjects, p < 0.05), while, at the end of O2 administration, it became higher in patients with COPD than in controls (1.62 +/- 0.4% in patients with COPD vs. 0.89 +/- 0.5 in control subjects, p < 0.001). In conclusion, our findings showed an oxygen-related increase of both the urinary Na+ excretion and the fractional excretion of filtered sodium in patients affected by COPD.


Drug Investigation | 1994

Influence of the Renin Profile on the Blood Pressure Response to Different Doses of Hydrochlorothiazide plus either Quinapril or Captopril

Claudio Ferri; Letizia Di Francesco; Alessandro Perrone; Roberta Baldoncini; Simonetta Coassin; Grazia Veneto; Gino Raule; Cesare Bellini

SummaryThe antihypertensive efficacy and safety of quinapril 20mg plus hydrochlorothiazide 6.25mg were compared over 8 weeks with Captopril 50mg plus hydrochlorothiazide 15mg in 52 patients with mild to moderate essential hypertension (27 men and 25 women age 49.7 ±8.4 years). The study also evaluated the relationship between antihypertensive efficacy and plasma renin activity/blood pressure sensitivity to changes in dietary sodium intake. The combination of quinapril or Captopril with hydrochlorothiazide showed similar antihypertensive effects and tolerability. Neither blood pressure salt sensitivity nor renin profile were predictive of blood pressure response to either therapy. These results suggest that the antihypertensive efficacy of an angiotensin converting enzyme inhibitor when administered in fixed ratio with a thiazide diuretic is independent of salt sensitivity in hypertension.


Atherosclerosis | 1985

Blood Lipid Profile in Healthy Subjects Treated with Ticlopidine

Francesco Violi; C. Alessandri; Luigi Iuliano; Andrea Ghiselli; Alessandro Perrone; F. Balsano

The study was carried out in order to evaluate if Ticlopidine induces lipid metabolism changes. Twenty seven healthy subjects were studied, 14 with placebo and 13 with Ticlopidine treatment (500 mg/day), for 30 days. Total cholesterol, HDL cholesterol, triglycerides, apolipoproteins A and B were evaluated before and after treatment. No significant changes of the blood lipid parameters were observed.


The Annals of Thoracic Surgery | 2005

Bronchoscopic lung-volume reduction with one-way valves in patients with heterogenous emphysema

Federico Venuta; Tiziano De Giacomo; Erino A. Rendina; Anna Maria Ciccone; Daniele Diso; Alessandro Perrone; Daniela Parola; Marco Anile; Giorgio Furio Coloni


Arteriosclerosis, Thrombosis, and Vascular Biology | 2006

Alpha-Linolenic Acid–Rich Wheat Germ Oil Decreases Oxidative Stress and CD40 Ligand in Patients With Mild Hypercholesterolemia

C. Alessandri; Pasquale Pignatelli; Lorenzo Loffredo; Luisa Lenti; Maria Del Ben; Roberto Carnevale; Alessandro Perrone; Domenico Ferro; Francesco Angelico; Francesco Violi

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F. Balsano

Sapienza University of Rome

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Cesare Bellini

Sapienza University of Rome

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Roberta Baldoncini

Sapienza University of Rome

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Simonetta Coassin

Sapienza University of Rome

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Anna Santucci

Brigham and Women's Hospital

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Claudio De Angelis

Sapienza University of Rome

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A. Santucci

University of L'Aquila

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Anna Maria Ciccone

Sapienza University of Rome

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C. Alessandri

Sapienza University of Rome

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