Insecticide Resistance in Mosquitoes and Root Maggots

1964 ◽  
Vol 96 (1-2) ◽  
pp. 100-101
Author(s):  
A. W. A. Brown ◽  
W. Klassen ◽  
M. K. K. Pillai ◽  
G. S. H. Hooper

This exhibit represents part of the work of the Department of Zoology in the past 5 years, and others who have contributed to it are F. Matsumura, Z. H. Abedi, T. Kimura, P. G. Fast, J. G. Towgood, J. N. Telford and N. H. Khan.The work with the mosquito Aedes aegypti has involved study of 8 susceptible strains. The mechanism of DDT-resistance has been found to be associated with its detoxication by an enzymic process of dehydrochlorination to DDE; the amount of DDE produced has been found to be directly proportional to the resistance level, both by experiments with larvae in vivo and with larval homogenates incubated with DDT and glutathione in vitro. A secondary resistance mechanism in American strains has been a very pronounced secretion and excretion of peritrophic membrane by the larvae.

1985 ◽  
Vol 27 (1) ◽  
pp. 23-28 ◽  
Author(s):  
H. R. Rathor ◽  
R. J. Wood

Aedes aegypti larvae and adults were selected to high levels of resistance with dichlorodiphenyltrichloroethane (DDT) along separate lines. The larval-selected line showed three responses associated with larval resistance: (i) increased detoxication of DDT by dehydrochlorination to dichlorodiphenyldichloroethane DDE (demonstrated both in vivo and in vitro), (ii) increased tolerance to unmetabolised ("residual") DDT and, (iii) a reduction in uptake of DDT. Larval selection caused very little change in adult resistance or the uptake of DDT by adults, but there was an increase in dehydrochlorination. In the adult-selected line dehydrochlorination was increased by selection and was significantly correlated with resistance.Key words: DDT, DDE, resistance, Aedes aegypti.


2018 ◽  
Vol 18 (2) ◽  
pp. 156-165 ◽  
Author(s):  
Jiaqiang Wang ◽  
Chien-shan Cheng ◽  
Yan Lu ◽  
Xiaowei Ding ◽  
Minmin Zhu ◽  
...  

Background: Propofol, a widely used intravenous anesthetic agent, is traditionally applied for sedation and general anesthesia. Explanation: Recent attention has been drawn to explore the effect and mechanisms of propofol against cancer progression in vitro and in vivo. Specifically, the proliferation-inhibiting and apoptosis-inducing properties of propofol in cancer have been studied. However, the underlying mechanisms remain unclear. Conclusion: This review focused on the findings within the past ten years and aimed to provide a general overview of propofol's malignance-modulating properties and the potential molecular mechanisms.


Lab on a Chip ◽  
2021 ◽  
Vol 21 (5) ◽  
pp. 795-820
Author(s):  
Andrea Spanu ◽  
Laura Martines ◽  
Annalisa Bonfiglio

This review focuses on the applications of organic transistors in cellular interfacing. It offers a comprehensive retrospective of the past, an overview of the latest innovations, and a glance on the future perspectives of this fast-evolving field.


1999 ◽  
Vol 202 (3) ◽  
pp. 247-252 ◽  
Author(s):  
T.M. Clark ◽  
A. Koch ◽  
D.F. Moffett

The ‘stomach’ region of the larval mosquito midgut is divided into histologically distinct anterior and posterior regions. Anterior stomach perfused symmetrically with saline in vitro had an initial transepithelial potential (TEP) of −66 mV (lumen negative) that decayed within 10–15 min to a steady-state TEP near −10 mV that was maintained for at least 1 h. Lumen-positive TEPs were never observed in the anterior stomach. The initial TEP of the perfused posterior stomach was opposite in polarity, but similar in magnitude, to that of the anterior stomach, measuring +75 mV (lumen positive). This initial TEP of the posterior stomach decayed rapidly at first, then more slowly, eventually reversing the electrical polarity of the epithelium as lumen-negative TEPs were recorded in all preparations within 70 min. Nanomolar concentrations of the biogenic amine 5-hydroxytryptamine (5-HT, serotonin) stimulated both regions, causing a negative deflection of the TEP of the anterior stomach and a positive deflection of the TEP of the posterior stomach. Phorbol 12,13-diacetate also caused a negative deflection of the TEP of the anterior stomach, but had no effect on the TEP of the posterior stomach. These data demonstrate that 5-HT stimulates region-specific ion-transport mechanisms in the stomach of Aedes aegypti and suggest that 5-HT coordinates the actions of the Malpighian tubules and midgut in the maintenance of an appropriate hemolymph composition in vivo.


2021 ◽  
Author(s):  
Ana Vitória Gomes Alves
Keyword(s):  

Introdução: A dengue é uma arbovirose tropical negligenciada mundialmente, transmitida pelo Aedes aegypti. A proteína não-estrutural 1 (NS1) está presente nos quatro sorotipos da dengue, e é um importante marcador de viremia na fase inicial da doença por ser secretada na circulação durante a replicação viral, está associada a doença clínica grave que se manifesta como febre hemorrágica da dengue (DHF) ou síndrome do choque da dengue pela indução de interleucina (IL) ‐10 e tem sido estudada além de biomarcador para diagnóstico, como alvo terapêutico. Objetivos: Descrever o uso da proteína não estrutural (NS1) para diagnóstico precoce da dengue e como potencial alvo terapêutico. Material e métodos: Foi realizado uma revisão da literatura, onde os artigos foram consultados nas bases de dados científicos: NCBI e Scielo, com os termos: “Dengue”, “NS1”, “Patogênese”, publicados entre 2014 e 2020. Resultados: Estudos mostram que a NS1 contribui na patogênese da doença, ao interagir com o endotélio e induzir vazamento vascular, uma característica clínica da dengue grave, também ativando o sistema complemento e induzindo citocinas imunossupressoras. Por isso, sua detecção precoce contribui para o diagnóstico/tratamento imediato, prevenindo a evolução para formas mais agressivas da doença. Essa proteína também pode ser utilizada para identificar quais pacientes tem chances de desenvolver febre hemorrágica, pois durante a fase inicial da doença os níveis de NS1 são mais altos. Tem sido recomendada a combinação da detecção do antígeno NS1 na circulação e dos anticorpos anti-NS1 para melhorar a sensibilidade e a especificidade do diagnóstico. Em estudos em camundongos, os anticorpos anti-NS1 podem reduzir a replicação viral de células infectadas, bloquear os efeitos patogênicos desencadeados por NS1 in vitro e em in vivo. Conclusão: É necessário o desenvolvimento de novos testes que aumentem a sensibilidade e especificidade do diagnóstico da NS1 e também tratamentos direcionados à NS1 que podem ser úteis na redução da gravidade da doença.


Author(s):  
Beate Gündel ◽  
Xinyuan Liu ◽  
Matthias Löhr ◽  
Rainer Heuchel

Pancreatic ductal adenocarcinoma (PDAC) is one of the most overlooked cancers despite its dismal median survival time of 6 months. The biggest challenges in improving patient survival are late diagnosis due to lack of diagnostic markers, and limited treatment options due to almost complete therapy resistance. The past decades of research identified the dense stroma and the complex interplay/crosstalk between the cancer- and the different stromal cells as the main culprits for the slow progress in improving patient outcome. For better ex vivo simulation of this complex tumor microenvironment the models used in PDAC research likewise need to become more diverse. Depending on the focus of the investigation, several in vitro and in vivo models for PDAC have been established in the past years. Particularly, 3D cell culture such as spheroids and organoids have become more frequently used. This review aims to examine current PDAC in vitro models, their inherent limitations, and their successful implementations in research.


2018 ◽  
Vol 69 (1) ◽  
pp. 711 ◽  
Author(s):  
I. SYMEONIDOU ◽  
E. BONOS ◽  
K. MOUSTAKIDIS ◽  
P. FLOROU-PANERI ◽  
E. CHRISTAKI ◽  
...  

Parasites (protozoa, helminthes, arthropods) represent a main threat for poultry worldwide. Among helminthes, nematodes constitute the most important group of parasites of poultry. The nematode Ascaridia galli, the cause of ascaridiosis in poultry, is one of the most important and prevalent parasites, resulting in serious economic losses, associated with the treatment cost, the decreased feed efficiency, and the poor egg and meat production. During the past few decades the indiscriminate use of anthelmintic drugs has generated several cases of resistance in helminthes in poultry, situation which is coupled with the severity of residues in poultry products. For this reason, nowadays attention has been drawn to the use of botanicals in poultry diet, due to their anthelmintic properties. Furthermore, the dietary use eco-friend ly of these plant derived substances compared to conventional synthetic anthelmintic drugs is considered as a natural and ecofriendly approach by the consumers. The focus of the present review is to recapitulate the studies, both in vivo and in vitro, that have demonstrated the anthelmintic efficacy of various dietary botanicals in controlling poultry ascaridiosis.


2021 ◽  
Vol 12 ◽  
Author(s):  
Ellen Menkhorst ◽  
Nandor Gabor Than ◽  
Udo Jeschke ◽  
Gabriela Barrientos ◽  
Laszlo Szereday ◽  
...  

Lectin-glycan interactions, in particular those mediated by the galectin family, regulate many processes required for a successful pregnancy. Over the past decades, increasing evidence gathered from in vitro and in vivo experiments indicate that members of the galectin family specifically bind to both intracellular and membrane bound carbohydrate ligands regulating angiogenesis, immune-cell adaptations required to tolerate the fetal semi-allograft and mammalian embryogenesis. Therefore, galectins play important roles in fetal development and placentation contributing to maternal and fetal health. This review discusses the expression and role of galectins during the course of pregnancy, with an emphasis on maternal immune adaptions and galectin-glycan interactions uncovered in the recent years. In addition, we summarize the galectin fingerprints associated with pathological gestation with particular focus on preeclampsia.


2021 ◽  
Vol 17 (10) ◽  
pp. 787-789
Author(s):  
Patrick W. Serruys ◽  
Ahmed Elkoumy ◽  
Osama Soliman
Keyword(s):  
The Past ◽  

2021 ◽  
Author(s):  
Jakub Kryczka ◽  
Joanna Boncela

Abstract Colorectal cancer (CRC) is one of the most prominent causes of cancer death worldwide. Chemotherapeutic regimens consisting of different drugs combinations such as 5-fluorouracil, and oxaliplatin (FOLFOX) or irinotecan (FOLFIRI) have been proven successful in the treatment of CRC. However, chemotherapy often leads to the acquisition of cancer drug resistance followed by metastasis and in the aftermath therapeutic failure. The molecular mechanism responsible for drug resistance is still unclear. The systemic search for new biomarkers of this phenomenon may identify new genes and pathways. To understand the drug resistance mechanism in CRC, the in vitro study based on the molecular analysis of drug-sensitive cells lines vs drug-resistant cells lines has been used. In our study to bridge the gap between in vitro and in vivo study, we compared the expression profiles of cell lines and patient samples from the publicly available database to select the new candidate genes for irinotecan resistance. Using The Gene Expression Omnibus (GEO) database of CRC cell lines (HT29, HTC116, LoVo, and their respective irinotecan-resistant variants) and patient samples (GSE42387, GSE62080, and GSE18105) we compared the changes in the mRNA expression profile of the main genes involved in irinotecan body’s processing, such as transport out of the cells and metabolism. Furthermore, using a protein-protein interaction network of differently expressed genes between FOLFIRI resistant and sensitive CRC patients, we have selected top networking proteins (upregulated: NDUFA2, SDHD, LSM5, DCAF4, and COX10, downregulated: RBM8A, TIMP1, QKI, TGOLN2, and PTGS2). Our analysis provided several potential irinotecan resistance markers, previously not described as such.


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