Jan Carlo Delorenzi

Prof. Dr. Jan Carlo Delorenzi

Universidade Presbiteriana Mackenzie, São Paulo, Brazil
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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1 May 2001 in Antimicrobial Agents and Chemotherapy
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Journal Article
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JDJan Carlo Delorenzi
Jan Carlo Delorenzi
MAMárcia Attias
Márcia Attias
CGCerli R. Gattass
Cerli R. Gattass
MAMarcelo Andrade
Marcelo Andrade
CRCláudia Rezende
Cláudia Rezende
ESElvira M. B. Saraiva
Elvira M. B. Saraiva
In this study, we show the leishmanicidal effects of a chloroform fraction (CLF) and a purified indole alkaloid obtained from crude stem extract ofPeschiera australisagainstLeishmania amazonensis, a causative agent of cutaneous leishmaniasis in the New World. In a bioassay-guided chemical fractionation, the leishmanicidal activity in CLF completely and irreversibly inhibited promastigote growth. This fraction was also active against amastigotes in infected murine macrophages. Chemical analysis of CLF identified an iboga-type indole alkaloid coronaridine as one of its major compounds. Coronaridine showed potent antileishmanial activity, inhibiting promastigote and amastigote growth. Promastigotes and amastigotes treated with CLF or coronaridine showed pronounced alterations in their mitochondria as assessed by transmission electron microscopy.

1 December 2011 in Phytochemistry
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Journal Article
Closed access
CFC. Ferreira
C. Ferreira
DSD.C. Soares
D.C. Soares
CBC.B. Barreto-Junior
C.B. Barreto-Junior
MNM.T. Nascimento
M.T. Nascimento
Leonardo Freire-de-LimaLeonardo Freire-de-Lima
Leonardo Freire-de-Lima
LPLucia Pinto-da-Silva
Lucia Pinto-da-Silva

1 July 2002 in Antimicrobial Agents and Chemotherapy
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Journal Article
Open access
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JDJan Carlo Delorenzi
Jan Carlo Delorenzi
Leonardo Freire-de-LimaLeonardo Freire-de-Lima
Leonardo Freire-de-Lima
CGCerli R. Gattass
Cerli R. Gattass
DCDeise de Andrade Costa
Deise de Andrade Costa
LHLiwen He
Liwen He
ESElvira Saraiva
Elvira Saraiva
In previous studies, we demonstrated the leishmanicide effect of coronaridine, a natural indole alkaloid isolated from stem bark ofPeschiera australis(Delorenzi et al., Antimicrob. Agents Chemother.45:1349-1354, 2001). In this study we show the leishmanicidal effect of the synthetic coronaridine and its racemic 18-methoxylated analog, 18-methoxycoronaridine. Both alkaloids revealed a potent leishmanicide effect againstLeishmania amazonensis, a causative agent of cutaneous and diffuse cutaneous leishmaniasis in the New World. Despite their potent leishmanicide effect, both alkaloids were neither toxic to murine macrophages nor did they modulate their oxidative or cytokine production responses.

1 June 2010 in Parasitology International
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Journal Article
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DSDeivid C. Soares
Deivid C. Soares
AAAlexandre L.S. Andrade
Alexandre L.S. Andrade
JDJan Carlo Delorenzi
Jan Carlo Delorenzi
JSJefferson Silva
Jefferson Silva
Leonardo Freire-de-LimaLeonardo Freire-de-Lima
Leonardo Freire-de-Lima
ESElvira Saraiva
Elvira Saraiva

1 June 2016 in Parasitology International
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Journal Article
Closed access
TMTahira Souza Melo
Tahira Souza Melo
CGCerli Rocha Gattass
Cerli Rocha Gattass
DSDeivid Costa Soares
Deivid Costa Soares
Micael CunhaMicael Cunha
Micael Cunha
CFChristian Ferreira
Christian Ferreira
JDJan Carlo Delorenzi
Jan Carlo Delorenzi

1 January 2012 in Experimental Diabetes Research
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Journal Article
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PFPatricia Fiorino
Patricia Fiorino
FEFabiana Evangelista
Fabiana Evangelista
FSFernando Santos
Fernando Santos
FMFátima Maria Motter Magri
Fátima Maria Motter Magri
JDJan Carlo Delorenzi
Jan Carlo Delorenzi
VFVera Farah
Vera Farah
We evaluated cardiac autonomic modulation by heart rate (HRV), and arterial pressure variability (APV), and metabolic response in streptozotocin diabetic rats treated with green tea. Male Wistar rats were separated in groups: control, drinking tap water (C), green tea-treated (GT) group, diabetic, drinking tap water (D), and diabetic, treated with green tea (DGT). Kidney mass was greater in D and DGT than in C and GT, but reduced in DGT compared to D. Green tea prevented the increase in creatinine clearance and reduced hyperglycemia in DGT compared to D. Arterial pressure was increased in GT and decreased in D compared to C. HRV was reduced in D compared with all groups. APV was decreased in D compared to C and recovery in DGT. Sympathetic modulation of APV was decreased in D compared with all groups. Green tea reduced hyperglycemia, prevented renal injury and autonomic dysfunction, suggesting reduced cardiovascular risk and target organ damage in diabetes.