Esperanza Meléndez-Herrera

Dr. Esperanza Meléndez-Herrera

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

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

Representative Publications

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26 June 2018 in Antioxidants
Verified
Journal Article
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EVEréndira Valencia-Avilés
Eréndira Valencia-Avilés
Martha-Estrella García-PérezMartha-Estrella García-Pérez
Martha-Estrella García-Pérez
MGMa Guadalupe Garnica-Romo
Ma Guadalupe Garnica-Romo
JCJuan de Dios FIGUEROA CARDENAS
Juan de Dios FIGUEROA CARDENAS
EMEsperanza Meléndez-Herrera
Esperanza Meléndez-Herrera
HMHector Martinez-Flores
Hector Martinez-Flores
The objective of this work was to determine the concentration of total phenols, total flavonoids, hydroxycinnamic acids, and proanthocyanidins present in crude extracts of Quercus laurina, Q. crassifolia, and Q. scytophylla bark. They were extracted by ethanol (90%) maceration and hot water. The antioxidant capacity was determined by the ability to capture OH•, O2•−, ROO•, H2O2, NO•, and HClO. The hot water crude extract of Q. crassifolia was chosen to be concentrated and purified due to its higher extraction yield (20.04%), concentration of phenol compounds (747 mg gallic acid equivalent (GAE)/g, 25.4 mg quercetin equivalent (QE)/g, 235 mg ChAE/g, 25.7 mg chlorogenic acid equivalents (ChAE)/g), and antioxidant capacity (expressed as half maximal effective concentration (EC50, µg/mL): OH• = 918, O2•− = 80.5, ROO• = 577, H2O2 = 597, NO• ≥ 4000, HClO = 740). In a second stage, Q. crassifolia extracted with hot water was treated with ethyl acetate, concentrating the phenol compounds (860 mg GAE/g, 43.6 mg QE/g, 362 ChAE/g, 9.4 cyanidin chloride equivalents (CChE)/g) and improving the scavenging capacity (OH• = 467, O2•− = 58.1, ROO• = 716, H2O2 = 22.0, NO• ≥ 4000, HClO = 108). Q. crassifolia had the highest polyphenolic concentration and the better capacity for scavenging reactive species, being a favorable candidate to be considered in the development of new products.

17 June 2019 in Journal of Food Science
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Journal Article
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EVEréndira Valencia-Avilés
Eréndira Valencia-Avilés
HMHector Martinez-Flores
Hector Martinez-Flores
Martha-Estrella García-PérezMartha-Estrella García-Pérez
Martha-Estrella García-Pérez
EMEsperanza Meléndez-Herrera
Esperanza Meléndez-Herrera
Martha-Estrella García-PérezMartha-Estrella García-Pérez
Martha-Estrella García-Pérez

1 March 2022 in Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology
Verified
Journal Article
Closed access
LRLiliana Areli Robledo-Avila
Liliana Areli Robledo-Avila
BPBryan Víctor Phillips-Farfán
Bryan Víctor Phillips-Farfán
MMMartha Harfush Meléndez
Martha Harfush Meléndez
LTLeonel Lopez Toledo
Leonel Lopez Toledo
DVDavid Tafolla Venegas
David Tafolla Venegas
EMEsperanza Meléndez-Herrera
Esperanza Meléndez-Herrera

13 June 2022 in Frontiers in Ecology and Evolution
Verified
Journal Article
Open access
NUNancy M. Unda-Díaz
Nancy M. Unda-Díaz
BPBryan V. Phillips-Farfán
Bryan V. Phillips-Farfán
HNHector Nava
Hector Nava
LLLeonel Lopez-Toledo
Leonel Lopez-Toledo
CMChiharu Murata
Chiharu Murata
EMEsperanza Meléndez-Herrera
Esperanza Meléndez-Herrera
Sea turtle egg relocation and hatchery incubation (hereafter termed ex situ incubation) is an effective strategy to protect clutches when in situ egg incubation is not viable. Nevertheless, it negatively affects the ontogenesis of male gonads and brain areas homologous to the mammalian hippocampus, as well as body size and fitness. Thus, it is imperative to analyze the effects of ex situ incubation on other developmental aspects and extend these observations to females. This work evaluated the effect of ex situ management on neurogenesis (cell proliferation in the dorsal and medial ventricular zones, neuronal integration in the dorsomedial and medial cortices), ovary cell proliferation, body size (mass and length) and self-righting ability. Additionally, this study examined if the incubation microenvironment is different between in situ and ex situ nests and whether it could contribute to explain the biological traits. An analysis of principal components showed differences in biological variables of hatchlings between in situ and ex situ clutches, driven by contrasting temperatures and silt composition. Each biological variable was also analyzed with linear mixed models using in situ vs. ex situ clutches, abiotic variables and their interaction. Turtles from ex situ clutches showed: (1) fewer proliferating cells in the dorsal and medial ventricular zones; (2) less mature neurons in the dorsomedial and medial cortices; (3) ovaries with a lesser number of proliferating cells; (4) lower body mass and length at emergence; and (5) slower self-righting time. Together, the results suggest that ex situ incubation in hatcheries is related to a slowing down of neurogenesis, ovariogenesis, body size and self-righting ability in hatchlings. Future studies should evaluate the effect of ex situ incubation on cognitive and reproductive performance to understand the long-term consequences of altered organogenesis. These studies should also disentangle the differential contribution of egg movement, reburial, nesting environment and parental origin to development. This information would likely result in better conservation strategies for sea turtles.

29 September 2022 in Frontiers in Ecology and Evolution
Verified
Journal Article
Open access
IVIvette Marai Villa-Villaseñor
Ivette Marai Villa-Villaseñor
BYBeatriz Yáñez-Rivera
Beatriz Yáñez-Rivera
RRRebeca Aneli Rueda-Jasso
Rebeca Aneli Rueda-Jasso
MHMa. Antonia Herrera-Vargas
Ma. Antonia Herrera-Vargas
RHRubén Hernández-Morales
Rubén Hernández-Morales
ODOmar Domínguez-Domínguez
Omar Domínguez-Domínguez
Nitrate-nitrogen (NO3-N) pollution related to anthropogenic activities is increasing in freshwater ecosystems. Knowledge about NO3-N sensitivity in freshwater wild fish is needed to understand the differential tolerance between species. Goodeinae is a subfamily of 41 endemic fishes that inhabit central Mexico, with 33 species in the IUCN red list and three extinct. Distributional patterns suggest tolerant and sensitive goodeines related to the conservation gradient of freshwater ecosystems. Four species with a differential distribution and tolerance were selected to evaluate their physiological responses to NO3-N. Fish were exposed to different NO3-N concentrations for 96 h and the median lethal concentration (LC50) was determined. Swimming disorders plus gill and liver histopathological indexes were estimated and incorporated into an Integrated Biomarker Response (IBR) for each species. Skiffia lermae (LC50 = 474.332 mg/L) and Xenotoca variata (LC50 = 520.273 mg/L) were more sensitive than Goodea atripinnis (LC50 = 953.049 mg/L) and Alloophorus robustus (LC50 = 1537.13 mg/L). The typical histological damage produced by NaNO3-N exposure was fusion of secondary lamellae in gills. This was present in all species and cellular degeneration was observed at the highest concentrations. Secondary lamellae aneurysms were only observed in G. atripinnis. Liver alterations included vascular dilation in hepatic sinusoids, hyperemia and nuclear hypertrophy; higher concentrations produced hepatocyte cytoplasmic vacuolation and reduced frequency of cell nuclei. Behavioral and histopathological alterations could explain the differential species sensitivity. The results suggest that species which preserve gill function and transfer the task of detoxification to the liver might have the best chance of surviving in polluted environments. Moreover, species previously considered as tolerant may be highly susceptible to NaNO3-N exposure. Therefore, it is necessary to closely monitor NaNO3-N concentrations in freshwater ecosystems and, if possible, reduce their levels to avoid the loss of wild populations.

19 June 2025 in Integrative Zoology
Verified
Journal Article
Closed access
IGIrma Yunuen García‐Bucio
Irma Yunuen García‐Bucio
BPBryan Víctor Phillips‐Farfán
Bryan Víctor Phillips‐Farfán
SCSandra Nataly Chávez‐Salazar
Sandra Nataly Chávez‐Salazar
MHMa. Antonia Herrera‐Vargas
Ma. Antonia Herrera‐Vargas
EVErnesto Vicente Vega‐Peña
Ernesto Vicente Vega‐Peña
EMEsperanza Meléndez-Herrera
Esperanza Meléndez-Herrera