Enantiomeric and Monoaminergic Contributions to Methamphetamine's Bidirectional Effects on Fentanyl-Depressed Respiration in Mice DOI Open Access
Harrison Elder,

D. Matthew Walentiny,

Patrick M. Beardsley

et al.

Authorea (Authorea), Journal Year: 2023, Volume and Issue: unknown

Published: Oct. 30, 2023

Rationale: Fentanyl remains the primary cause of fatal overdoses, and its co-use with methamphetamine (METH) is a growing concern. The optical isomers METH, dextromethamphetamine (d-METH) levomethamphetamine (l-METH), differ substantially in dose expression thus may differentially contribute to racemate’s bidirectional effects. Furthermore, it unknown which METH’s monoamine (MA) receptor mechanisms mediate these respiratory Thus, systematic evaluation selective agents identify treatment targets for OIRD. Methods: two d-METH l-METH, were tested adult male mice determine their effects on basal fentanyl-depressed minute volume (MVb; i.e., frequency x tidal volum) using whole-body plethysmography. Next, six agonists at MA receptors involved activity [phenylephrine (PNE; α1), clonidine (CLON; α2), SKF-82958 (SKF; D1), quinpirole (QPR; D2), 8-OH-DPAT (8-OH; 5HT1A), DOI (5HT2)] singly MVb, then combination fentanyl. Results: elevated MVb l-METH decreased MVb. Under conditions, racemic METH recreated by while significantly exacerbated OIRD 1.0 3.0 mg/kg. was dose-dependently increased PNE SKF CLON QPR. Neither 8-OH nor altered transiently more persistently it, Conclusions: modulation observed racemate activation respiration

Language: Английский

Endogenous opiates and behavior: 2023 DOI
Richard J. Bodnar

Peptides, Journal Year: 2024, Volume and Issue: 179, P. 171268 - 171268

Published: June 28, 2024

Language: Английский

Citations

5

Enantiomeric contributions to methamphetamine's bidirectional effects on basal and fentanyl-depressed respiration in mice DOI Creative Commons
Harrison Elder,

D. Matthew Walentiny,

Patrick M. Beardsley

et al.

Pharmacology Biochemistry and Behavior, Journal Year: 2024, Volume and Issue: 238, P. 173735 - 173735

Published: Feb. 17, 2024

Language: Английский

Citations

4

Monoamine receptors targeted by methamphetamine differentially modulate basal and fentanyl-depressed respiration in mice DOI
Harrison Elder,

D. Matthew Walentiny,

Patrick M. Beardsley

et al.

Pharmacology Biochemistry and Behavior, Journal Year: 2025, Volume and Issue: unknown, P. 174004 - 174004

Published: March 1, 2025

Language: Английский

Citations

0

Progress in Methylxanthine Biosynthesis: Insights into Pathways and Engineering Strategies DOI Open Access
Tongtong Jiang,

Shangci Zuo,

Chang Yu Liu

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(4), P. 1510 - 1510

Published: Feb. 11, 2025

Methylxanthines are ubiquitous purine alkaloids in nature and have rich biological activities functions. Today, the demand for methylxanthine is increasing but its production low. This issue prevents widespread use many industrial fields, such as pharmaceuticals, food manufacturing, chemical engineering. To address these issues, this review provides a comprehensive systematic exploration of methylxanthines, delving into their structures, detailed biosynthetic pathways, latest research trends. These findings serve valuable references researchers, fostering advancements optimization synthesis processes methylxanthines derivatives promoting application across diverse medicine, food, By bridging fundamental practical applications, work aims to advance understanding compounds, enhance efficiency, contribute healthcare technological progress.

Language: Английский

Citations

0

Fentanyl Overdose Causes Prolonged Cardiopulmonary Dysregulation in Male SKH1 Mice DOI Creative Commons

Mackenzie Newman,

Heather Connery,

Swapna Kannan

et al.

Pharmaceuticals, Journal Year: 2024, Volume and Issue: 17(7), P. 941 - 941

Published: July 14, 2024

Fentanyl overdose is a survivable condition that commonly resolves without chronic overt changes in phenotype. While the acute physiological effects of fentanyl overdose, such as opioid-induced respiratory depression (OIRD) and Wooden Chest Syndrome, represent immediate risks lethality, little known about longer-term systemic or organ-level impacts for survivors. In this study, we investigated single, bolus on components cardiopulmonary system up to one week post. SKH1 mice were administered subcutaneous at highest non-lethal dose (62 mg/kg), LD10 (110 LD50 (135 before euthanasia 40 min, 6 h, 24 7 d post-exposure. The cerebral cortex, heart, lungs, plasma assayed using an immune monitoring 48-plex panel. results showed significantly dysregulated cytokine, chemokine, growth factor concentrations compared time-matched controls, principally hearts, then lungs lesser extent, length with cortex largely unaffected. Major significant analytes contributing variance included eotaxin-1, IL-33, betacellulin, which generally downregulated across time. study suggest toxicity may persist from single have wide implications endurance expanding population

Language: Английский

Citations

0

Enantiomeric and Monoaminergic Contributions to Methamphetamine's Bidirectional Effects on Fentanyl-Depressed Respiration in Mice DOI Open Access
Harrison Elder,

D. Matthew Walentiny,

Patrick M. Beardsley

et al.

Authorea (Authorea), Journal Year: 2023, Volume and Issue: unknown

Published: Oct. 30, 2023

Rationale: Fentanyl remains the primary cause of fatal overdoses, and its co-use with methamphetamine (METH) is a growing concern. The optical isomers METH, dextromethamphetamine (d-METH) levomethamphetamine (l-METH), differ substantially in dose expression thus may differentially contribute to racemate’s bidirectional effects. Furthermore, it unknown which METH’s monoamine (MA) receptor mechanisms mediate these respiratory Thus, systematic evaluation selective agents identify treatment targets for OIRD. Methods: two d-METH l-METH, were tested adult male mice determine their effects on basal fentanyl-depressed minute volume (MVb; i.e., frequency x tidal volum) using whole-body plethysmography. Next, six agonists at MA receptors involved activity [phenylephrine (PNE; α1), clonidine (CLON; α2), SKF-82958 (SKF; D1), quinpirole (QPR; D2), 8-OH-DPAT (8-OH; 5HT1A), DOI (5HT2)] singly MVb, then combination fentanyl. Results: elevated MVb l-METH decreased MVb. Under conditions, racemic METH recreated by while significantly exacerbated OIRD 1.0 3.0 mg/kg. was dose-dependently increased PNE SKF CLON QPR. Neither 8-OH nor altered transiently more persistently it, Conclusions: modulation observed racemate activation respiration

Language: Английский

Citations

0