Of the known biochemical actions of caffeine, only inhibition of adenosine receptors occurs at concentrations achieved during normal human consumption of the drug. Under normal physiological conditions, adenosine is present in sufficient concentrations to activate A1 and A2a receptors. Via actions on A1 receptors, adenosine decreases neuronal firing and the release of neurotransmitters. The exact…
Pharmacology & Toxicology Template
Write in a clean editor, then format for Pharmacology & Toxicology in one click — DocuGuru applies the official Wiley template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the Pharmacology & Toxicology format
Pharmacology & Toxicology is a peer-reviewed journal published by Wiley, covering Neuroscience and Neuropharmacology Research, Receptor Mechanisms and Signaling, Pharmacogenetics and Drug Metabolism.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Pharmacology & Toxicology 12 (3): 45–58.
Formats any DOI in Pharmacology & Toxicology style. No sign-up. |
| Publishes research in | Neuroscience and Neuropharmacology Research Receptor Mechanisms and Signaling Pharmacogenetics and Drug Metabolism Neurotransmitter Receptor Influence on Behavior Ion channel regulation and function |
| ISSN | 0901-9928 |
| h-index | 89 |
| i10-index | 1,436 |
| Total citations | 55,974 |
| Top institutions publishing here | Karolinska Institutet |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Pharmacology & Toxicology per year
Citation impact of Pharmacology & Toxicology by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Pharmacology & Toxicology
Sodium selenite (Na2SeO3) is the selenium form used in the composition of dietary supplements, and diphenyl diselenide (PhSe)2 is an important intermediate in organic synthesis, which increases the risk of human exposure to this chemical in the workplace. These compounds have been reported to inhibit the cerebral and hepatic aminolevulinic acid dehydratase (ALA-D) in vitro,…
Certain types of neuronal ions channels have been demonstrated to be the major target sites of insecticides. The insecticide-channel interactions that have been studied most extensively are pyrethroid actions on the voltage-gated sodium channel and cyclodiene/lindane actions on the GABAA receptor chloride channel complex. With the exception of organophosphate and carbamate insecticides which inhibit acetylcholinesterases,…
Doxorubicin (Adriamycin) is a potent and broad-spectrum antineoplastic agent prescribed for the treatment of a variety of cancers, including both solid tumours and leukaemias. Unfortunately, despite its broad effectiveness, long-term therapy with doxorubicin is associated with a high incidence of a cumulative and irreversible dilated cardiomyopathy. Numerous mechanisms have been proposed to account for this…
Metabolism of methanol, methyl ethers, esters and amides give rise to formic acid. This acid is an inhibitor of the mitochondrial cytochrome oxidase causing histotoxic hypoxia. Formic acid is a weaker inhibitor than cyanide and hydrosulphide anions. The body burden of formate in methanol poisoning is high enough to cause acidosis, and other clinical symptoms.…