Results 21 to 30 of about 13,009 (197)

The monocarboxylate transporter family—Role and regulation [PDF]

open access: yesIUBMB Life, 2011
AbstractMonocarboxylate transporter (MCT) isoforms 1–4 catalyze the proton‐linked transport of monocarboxylates such as L‐lactate across the plasma membrane, whereas MCT8 and MCT10 are thyroid hormone and aromatic amino acid transporters, respectively.
Halestrap, AP, Wilson, MC
openaire   +3 more sources

Monocarboxylate transporter functions and neuroprotective effects of valproic acid in experimental models of amyotrophic lateral sclerosis

open access: yesJournal of Biomedical Science, 2022
Background Amyotrophic lateral sclerosis (ALS) is a devasting neurodegenerative disorder for which no successful therapeutics are available. Valproic acid (VPA), a monocarboxylate derivative, is a known antiepileptic drug and a histone deacetylase ...
Asmita Gyawali   +5 more
doaj   +1 more source

Monocarboxylate transporters: past, present, and future.

open access: yesHistology and histopathology, 2008
We review here the 14 members of the Monocarboxylate transporter family (MCTs), their relationship based on sequence homology. The range of substrates transported by different members of this family extends from the standard monocarboxylate metabolites, lactic and pyruvic acids, to aromatic amino acids and thyroid hormones. The family is denoted Solute
Merezhinskaya, Natalya   +1 more
openaire   +3 more sources

Lactate transport in red blood cells by monocarboxylate transporters [PDF]

open access: yesEquine Veterinary Journal, 2002
Summary The lactate transport activity of red blood cells (RBC) varies widely among different species; in equine RBC, the activity of the main lactate carrier, H + ‐monocarboxylate co‐transporter (MCT), is distributed bimodally. The influence of lactate transport activity is
N M, Koho, L K, Väihkönen, A R, Pösö
openaire   +2 more sources

Monocarboxylate Transporter 1 (MCT1) in Liver Pathology [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
Membrane monocarboxylate transporter 1 (SLC16A1/MCT1) plays an important role in hepatocyte homeostasis, as well as drug handling. However, there is no available information about the impact of liver pathology on the transporter levels and function. The study was aimed to quantify SLC16A1 mRNA (qRT-PCR) and MCT1 protein abundance (liquid chromatography–
Marek Droździk   +8 more
openaire   +2 more sources

IMMUNOHISTOCHEMICAL EXPRESSION OF MONOCARBOXYLATE TRANSPORTER 1&4 IN TANYCYTE–LIKE CELLS OF THE SULCUS MEDIANUS ORGANUM

open access: yesThe Iraqi Journal of Medical Sciences, 2019
Background: Circumventricular organs (CVOs) are specialized structures border the brain ventricles and lack the blood-brain barrier. These CVOs are lined by specialized ependymal cells (ECs) called tanycyte.
Haider F. Jawad   +2 more
doaj   +6 more sources

Adipocytes promote malignant growth of breast tumours with monocarboxylate transporter 2 expression via β-hydroxybutyrate

open access: yesNature Communications, 2017
Invasion of the adipose tissue correlates with poor prognosis in breast cancer. Here, the authors show that mammary gland adipocytes promote malignancy via β-hydroxybutyrate, which acts on cancer cells through the monocarboxylate transporter MCT2 ...
Chun-Kai Huang   +8 more
doaj   +1 more source

Intestinal OCTN2- and MCT1-targeted drug delivery to improve oral bioavailability

open access: yesAsian Journal of Pharmaceutical Sciences, 2020
Various drug transporters are widely expressed throughout the intestine and play important roles in absorbing nutrients and drugs, thus providing high quality targets for the design of prodrugs or nanoparticles to facilitate oral drug delivery.
Gang Wang   +8 more
doaj   +1 more source

Exercise-induced hyperinsulinism: genetic basis and clinical management

open access: yes中国当代儿科杂志
Exercise-induced hyperinsulinism, also known as monocarboxylate transporter 1 hyperinsulinemia, is a rare subtype of congenital hyperinsulinism caused by gain-of-function variants in the SLC16A1 gene, which encodes monocarboxylate transporter 1.
ZHANG Qi-Ting, HOU Ling
doaj   +1 more source

Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out

open access: yesStem Cell Research, 2023
The X-linked Allan-Herndon-Dudley syndrome (AHDS) is characterized by severely impaired psychomotor development and is caused by mutations in the SLC16A2 gene encoding the thyroid hormone transporter MCT8 (monocarboxylate transporter 8).
Katarzyna Anna Ludwik   +7 more
doaj   +1 more source

Home - About - Disclaimer - Privacy