Roberta d'Emmanuele di Villa Bianca

Prof. Dr. Roberta d'Emmanuele di Villa Bianca

Department of Pharmacy, School of Medicine and Surgery, University of Naples, Federico II, Via D. Montesano, 49, 80131, Naples, Italy

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2020 in Pharmacology & Therapeutics
Verified
Journal Article
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EMEmma Mitidieri
Emma Mitidieri
GCGiuseppe Cirino
Giuseppe Cirino
Roberta d'Emmanuele di Villa BiancaRoberta d'Emmanuele di Villa Bianca
Roberta d'Emmanuele di Villa Bianca
RAFFAELLA SORRENTINORAFFAELLA SORRENTINO
RAFFAELLA SORRENTINO

1 May 2018 in Nitric Oxide
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Journal Article
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EMEmma Mitidieri
Emma Mitidieri
TTTeresa Tramontano
Teresa Tramontano
DGDanila Gurgone
Danila Gurgone
VCValentina Citi
Valentina Citi
VCVincenzo Calderone
Vincenzo Calderone
RAFFAELLA SORRENTINORAFFAELLA SORRENTINO
RAFFAELLA SORRENTINO

Verified
Journal Article
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RRRosaria Margherita Rispoli
Rosaria Margherita Rispoli
APAda Popolo
Ada Popolo
VFVincenzo De Fabrizio
Vincenzo De Fabrizio
Roberta d'Emmanuele di Villa BiancaRoberta d'Emmanuele di Villa Bianca
Roberta d'Emmanuele di Villa Bianca
GAGiuseppina Autore
Giuseppina Autore
STEFANIA MARZOCCOSTEFANIA MARZOCCO
STEFANIA MARZOCCO
Chronic kidney disease (CKD) is a condition caused by the gradual decline of renal function that approximatively affects 10–12% of the world population, thus representing a public health priority. In CKD patients, chronic and systemic low-grade inflammation is observed, and it significantly contributes to disease development and progression, especially for patients with advanced disease. It also results in CKD-associated complications and increased mortality. The low-grade inflammation is due to different factors, such as the decline of glomerular filtration rate, increased immune system activation, reactive oxygen species release, and intestinal homeostasis. Therefore, the possibility to control chronic low-grade inflammation in CKD deserves great attention. In this review, we will examine the current possible pharmacological approaches to counteract the inflammatory state in CKD, focusing our attention both on the pro-inflammatory factors and the pro-resolving mediators involved in CKD inflammatory state.

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VMVincenzo Mirone
Vincenzo Mirone
LNLuigi Napolitano
Luigi Napolitano
Roberta d'Emmanuele di Villa BiancaRoberta d'Emmanuele di Villa Bianca
Roberta d'Emmanuele di Villa Bianca
EMEmma Mitidieri
Emma Mitidieri
RAFFAELLA SORRENTINORAFFAELLA SORRENTINO
RAFFAELLA SORRENTINO
GCGiuseppe Cirino
Giuseppe Cirino
Objective: To assess the efficacy of the combination of Tadalafil 5 mg and nutritional supplements composed by Panax ginseng, Moringa Oleifera and Rutin on erectile function in men with mild and moderate vasculogenic ED.Methods: we prospectively enrolled 86 patients divided into two groups A (45), B (33) in this multicenter randomized, doubleblind, placebo-controlled trial . Drop out was 8 patients (3 patients in group A and 5 in Group B). At screening visit patients underwent clinical examination, blood test (hormonal and metabolic profile) and filled out the IIEF-5 questionnaire and the SEP-2, SEP-3. Patients were randomized by a computergenerated list to receive either Tadalafil 5 mg once daily plus nutritional supplement once daily (group A) or Tadalafil 5 mg plus placebo with the same administration schedule (group B) for 3 months. Blood samples, IIEF-5, SEP-2 and SEP-3 have been collected again after 3 months. cGMP was measured in platelets of 38 patients at baseline and after one months. Results: Mean age was 59.98 ± 6.90 (range 38-69), mean IIEF-5 score at baseline was 13.59 ± 3.90. After three months of treatment, IIEF-5 score significantly improved in both groups compared to baseline (13.18 ± 3.75 vs 20.48 ± 2.24, p < 0.0001; 14.15 ± 4.09 vs 19.06 ± 4.36, p < 0.0001, in group A and group B respectively). Patients treated with Tadalafil plus nutritional supplement showed a significantly higher increase in IIEF-5 score compared to those who received placebo (7.27 ± 2.20 and 4.9 ± 2.79, respectively; p < 0.0001;). No hormonal differences and metabolic effects were found. According cGMP result, nutritional supplements ameliorates and extends the activity of the chronic treatment. Conclusions: IIEF-5 significant increase in group B, can be ascribed to the nutritional supplement properties and antioxidant effects of moringa oleifera, ginseng and rutin and this can enhance the endothelial NO and cGMP production.

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IBIvana Bello
Ivana Bello
MSMartina Smimmo
Martina Smimmo
Roberta d'Emmanuele di Villa BiancaRoberta d'Emmanuele di Villa Bianca
Roberta d'Emmanuele di Villa Bianca
Mariarosaria BucciMariarosaria Bucci
Mariarosaria Bucci
GCGiuseppe Cirino
Giuseppe Cirino
Vincenzo BrancaleoneVincenzo Brancaleone
Vincenzo Brancaleone
Breast cancer is the most frequent form of cancer occurring in women of any age. Among the different types, the triple-negative breast cancer (TNBC) subtype is recognized as the most severe form, being associated with the highest mortality rate. Currently, there are no effective treatments for TNBC. For this reason, the research of novel therapeutics is urgently needed. Natural products and their analogs have historically made a major contribution to pharmacotherapy and the treatment of various human diseases, including cancer. In this study, we explored the potential anti-cancer effects of erucin, the most abundant H2S-releasing isothiocyanate present in arugula (Eruca sativa) in MDA-MB-231 cells, a validated in vitro model of TNBC. We found that erucin, in a concentration-dependent manner, significantly inhibited MDA-MB-231 cell proliferation by inducing apoptosis and autophagy. Additionally, erucin prevented intracellular ROS generation promoting the expression of key antioxidant genes and halted MDA-MB-231 cell migration, invasion, and colony formation. In conclusion, using a cellular and molecular biology approach, we show that the consumption of erucin could represent a novel and promising strategy for intervention against TNBC.

19 June 2023 in Pharmacological Research
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Journal Article
Open access
MOMiguel A. Olivencia
Miguel A. Olivencia
EEErika Esposito
Erika Esposito
VBVincenzo Brancaleone
Vincenzo Brancaleone
SCSigismondo Castaldo
Sigismondo Castaldo
GCGiuseppe Cirino
Giuseppe Cirino
EMEmma Mitidieri
Emma Mitidieri
The corpus cavernosum (CC) is a highly vascularized tissue and represents an excellent example of microcirculation. Indeed, erectile dysfunction is considered an early index of cardiovascular disease. Hydrogen sulfide (H2S) at the vascular level is endogenously produced from L-cysteine mainly by the action of cystathionine-γ-lyase (CSE) and plays a role in CC vascular homeostasis. Here we have evaluated the involvement of the endogenous H2S in the regulation of the soluble guanylate cyclase (sCG) redox state. The lack of CSE-derived endogenous H2S, in CSE-/- mice, disrupted the eNOS/NO/sGC/PDE pathway. Indeed, the absence of CSE-derived endogenous H2S caused a significant reduction of the relaxant response to riociguat, an sGC redox-dependent stimulator. Conversely, the response to cinaciguat, an sGC redox-independent activator, was not modified. The relevance of the role played at the redox level of the endogenous H2S was confirmed by the findings that in CC harvested from CSE-/- mice there was a significant reduction of GCβ1 expression coupled with a decrease in CYP5R3, a reductase involved in the regulation of the redox state of sGC. These molecular changes driven by the lack of endogenous H2S translate into a significant reduction in cGMP levels. The replenishment of the lack of H2S with an H2S donor rescued the relaxant response to riociguat in CC of CSE-/- mice. In conclusion, the endogenous CSE-derived H2S plays a physiological key role in the regulation of the redox state of sGC in CC microcirculation.