Juan Rodrigo Salazar

Dr. Juan Rodrigo Salazar

Universidad La Salle Mexico
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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23 October 2018 in Biomolecules
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MLMarco A. Loza-Mejía
Marco A. Loza-Mejía
Juan Rodrigo SalazarJuan Rodrigo Salazar
Juan Rodrigo Salazar
JSJuan Francisco Sánchez-Tejeda
Juan Francisco Sánchez-Tejeda
An increasing occurrence of resistance in insect pests and high mammal toxicity exhibited by common pesticides increase the need for new alternative molecules. Among these alternatives, bioinsecticides are considered to be environmentally friendly and safer than synthetic insecticides. Particularly, plant extracts have shown great potential in laboratory conditions. However, the lack of studies that confirm their mechanisms of action diminishes their potential applications on a large scale. Previously, we have reported the insect growth regulator and insecticidal activities of secondary metabolites isolated from plants of the Calceolaria genus. Herein, we report an in silico study of compounds isolated from Calceolaria against acetylcholinesterase, prophenoloxidase, and ecdysone receptor. The molecular docking results are consistent with the previously reported experimental results, which were obtained during the bioevaluation of Calceolaria extracts. Among the compounds, phenylethanoid glycosides, such as verbascoside, exhibited good theoretical affinity to all the analyzed targets. In light of these results, we developed an index to evaluate potential multitarget insecticides based on docking scores.


29 January 2021 in Molecules
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Alonso Vivar-SierraAlonso Vivar-Sierra
Alonso Vivar-Sierra
MAMaría José Araiza-Macías
María José Araiza-Macías
JHJosé Patricio Hernández-Contreras
José Patricio Hernández-Contreras
AVArely Vergara-Castañeda
Arely Vergara-Castañeda
GRGabriela Ramírez-Vélez
Gabriela Ramírez-Vélez
MLMarco A. Loza-Mejía
Marco A. Loza-Mejía
SARS-CoV-2 infects host cells by interacting its spike protein with surface angiotensin-converting enzyme 2 (ACE2) receptors, expressed in lung and other cell types. Although several risk factors could explain why some countries have lower incidence and fatality rates than others, environmental factors such as diet should be considered. It has been described that countries with high polyunsaturated fatty acid (PUFA) intake have a lower number of COVID-19 victims and a higher rate of recovery from the disease. Moreover, it was found that linoleic acid, an omega-6 PUFA, could stabilize the spike protein in a closed conformation, blocking its interaction with ACE2. These facts prompted us to perform in silico simulations to determine if other PUFA could also stabilize the closed conformation of spike protein and potentially lead to a reduction in SARS-CoV-2 infection. We found that: (a) countries whose source of omega-3 is from marine origin have lower fatality rates; and (b) like linoleic acid, omega-3 PUFA could also bind to the closed conformation of spike protein and therefore, could help reduce COVID-19 complications by reducing viral entrance to cells, in addition to their known anti-inflammatory effects.

1 February 2001 in Zeitschrift für Naturforschung C
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Journal Article
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Carlos L CespedesCarlos L Cespedes
Carlos L Cespedes
MMMariano Martínez-Vázquez
Mariano Martínez-Vázquez
JCJose S. Calderón
Jose S. Calderón
Juan Rodrigo SalazarJuan Rodrigo Salazar
Juan Rodrigo Salazar
EAEduardo Aranda
Eduardo Aranda
Argentatins, Insect Growth Regulators, Acetylcholinesterase The methanolic extract from aerial parts of Parthenium argentatum, afforded argentatin A and B. These compounds were evaluated for their effect on the fall armyworm (Spodoptera frugiperda). Toosendanin, a commercial insecticide derived from Melia azedarach was used as positive control. When tested for activity, using neonate larvae into the no-choice artificial diet bioassays, argentatin A, argentatin B and methanol extract caused significant growth inhibitory activity with GC50 of 17.8, 36.1 and 6.4 ppm at 7 days, respectively, and increased the development time of surviving larvae in a concentration-dependent manner with RGI values of 0.40, 0.60 and 0.26, at 25.0, 25.0 and 5.0 ppm. respectively. In addition, it was possible to observe in most of the treated groups a significant delay in the time of pupation, adult emergence and deformities. Acute toxicity against adults of S. frugiperda was also found, MeOH extract had the most potent activity with LD50 value of 3.10 ppm. In addition, MeOH extract and argentatin A caused acetylcholinesterase inhibition of 93.7% and 90.0%, at 5.0 and 50.0 ppm, respectively; whereas argentatin B had only slight inhibitory activity. Therefore, the MeOH extract was identified as insecticidal extract from P. argentatum with activity at concentrations above 15.0 ppm.

19 February 2013 in Phytochemistry Reviews
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Carlos L CespedesCarlos L Cespedes
Carlos L Cespedes
CLCarlos L.
Carlos L.
Juan Rodrigo SalazarJuan Rodrigo Salazar
Juan Rodrigo Salazar
JAJulio Alarcon
Julio Alarcon