5-Methoxyindole-2-Carboylic Acid (MICA) Fails to Retard Development and Progression of Type II Diabetes in ZSF1 Diabetic Rats.

React Oxyg Species (Apex)

Department of Pharmaceutical Sciences, UNT System College of Pharmacy, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.

Published: May 2020

5-Methoxyindole-2-carboxylic acid (MICA) is a well-established reversible inhibitor of mitochondrial dihydrolipoamide dehydrogenase (DLDH). This chemical, as an indole derivative, has been shown to be neuroprotective against ischemic stroke injury when administered either before or after ischemic stroke in animal models. MICA has also been studied as a potential antidiabetic agent by numerous investigators, though the underlying mechanisms remain sketchy. To attempt to elucidate the mechanisms of its antidiabetic action, we tested the effect of MICA on ZSF1 rat, a widely used rodent model of type 2 diabetes. ZSF1 rats as well as its healthy controls were fed with control diet or MICA-containing diet (200 mg/kg/day) for 9 weeks. Unexpectedly, comparison of body weight changes and blood glucose levels at the end of the 9-week's feeding period indicated that MICA failed to show any anti-diabetic effect in the ZSF1 diabetic rats. The reasons for this failure were discussed.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301685PMC

Publication Analysis

Top Keywords

acid mica
8
type diabetes
8
diabetes zsf1
8
zsf1 diabetic
8
diabetic rats
8
ischemic stroke
8
mica
5
5-methoxyindole-2-carboylic acid
4
mica fails
4
fails retard
4

Similar Publications

Phage-mediated intercellular CRISPRi for biocomputation in bacterial consortia.

Nucleic Acids Res

December 2024

Université Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, 78350 Jouy-en-Josas, France.

Coordinated actions of cells in microbial communities and multicellular organisms enable them to perform complex tasks otherwise difficult for single cells. This has inspired biological engineers to build cellular consortia for larger circuits with improved functionalities while implementing communication systems for coordination among cells. Here, we investigate the signalling dynamics of a phage-mediated synthetic DNA messaging system and couple it with CRISPR interference to build distributed circuits that perform logic gate operations in multicellular bacterial consortia.

View Article and Find Full Text PDF

Tuning the nanostructure and tribological properties of a non-ionic deep eutectic solvent with water addition.

J Colloid Interface Sci

December 2024

School of Molecular Sciences, The University of Western Australia, Perth, WA 6009, Australia; Centre for Microscopy, Characterisation and Analysis, The University of Western Australia, Perth, WA 6009, Australia. Electronic address:

Hypothesis: The addition of water to a non-ionic N-oxide deep eutectic solvent(DES) composed of phenylacetic acid (PhAA) and N-dodecylmorpholine-N-oxide(MO-12) in a 1:1 M ratio(PhAA/MO-12) will promote interfacial nanostructure formation due to increased proton transfer and solvophobic interactions, leading to reduced friction.

Experiments: The interfacial structure and friction of PhAA/MO-12 with water content up to 41.9 wt% were investigated at mica surfaces.

View Article and Find Full Text PDF

Control over the orientation of polycyclic aromatic dyes in thin films is paramount to tailoring their optical, electronic, and mechanical properties. Their supramolecular assembly in films is tuned here by converting the macrocyclic dyes to large amphiphiles. Two octaalkythio-substituted tetraazaporphyrins (TAPs) with one 5-carboxypentyl and one pentyl or dodecyl chain per pyrrole ring were synthesized as statistical mixtures of four regioisomers.

View Article and Find Full Text PDF

canSAR (https://cansar.ai) continues to serve as the largest publicly available platform for cancer-focused drug discovery and translational research. It integrates multidisciplinary data from disparate and otherwise siloed public data sources as well as data curated uniquely for canSAR.

View Article and Find Full Text PDF
Article Synopsis
  • Intratumoral injection of CAR-T cells for melanoma treatment offers reduced systemic side effects and higher CAR-T cell concentration, but challenges like few targeting ligands and a tough tumor microenvironment (TME) hinder effectiveness.
  • A novel nanogel, HA-Mn-CAP Gel, was developed to target receptors in melanoma, releasing manganese to alleviate tumor hypoxia and boost CAR-T cell ligand expression, showing over a 2.7 times increase in NKGD ligand levels in melanoma cells.
  • When combined with CAR-T therapy, HA-Mn-CAP Gel enhanced T cell proliferation and infiltration, increasing tumor inhibition rates significantly, suggesting this approach could improve therapies for solid tumors.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!