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Related Concept Videos

Toxicity Testing in Animals01:23

Toxicity Testing in Animals

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Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
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Toxic Reactions: Overview01:26

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When toxic substances penetrate the human body, they disseminate to various tissues, undergoing metabolic changes. This process yields reactive metabolites that may covalently bind with specific target molecules, resulting in toxicity.
Toxicity falls into two primary categories: local and systemic.
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Drug Toxicity: Overview01:00

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Drug toxicity quantifies the harm a compound causes to an organism, varying by dose and potentially impacting whole systems or specific organs like the liver. Toxic reactions may arise from venomous insect or spider bites, with effects ranging from mild symptoms to severe outcomes such as brain damage or death. Common forms of acute poisoning include ethanol intoxication and overdose of pain or fever medications, with substances like GHB and heroin being particularly lethal at doses close to...
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Bioactivation and Tissue Toxicity01:25

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Bioactivation is a metabolic process that transforms less reactive substances into highly reactive metabolites, initiating tissue toxicity. This transformation can lead to various toxic effects, including carcinogenesis and teratogenesis. Reactive metabolites are classified into two main types: electrophiles and free radicals.Electrophiles are electron-deficient species and are produced primarily by the enzyme cytochrome P-450 during the metabolism of compounds containing carbon, nitrogen, or...
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Drug Toxicity: Risk factors01:24

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Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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Drug toxicity: Idiosyncratic Reactions01:16

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Idiosyncratic drug reactions represent abnormal chemical responses that vary significantly among individuals, ranging from extreme sensitivity to low doses to insensitivity to high doses. These reactions often occur due to the drug's covalent binding with serum proteins, forming a foreign hapten that triggers an immunotoxicological response. The variability in drug reactions has a strong pharmacogenetic foundation, with genetic differences crucial in how individuals metabolize drugs. For...
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Measuring RAN Peptide Toxicity in C. elegans
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Is LSD toxic?

David E Nichols1, Charles S Grob2

  • 1Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA.

Forensic Science International
|February 7, 2018
PubMed
Summary
This summary is machine-generated.

Lysergic acid diethylamide (LSD) is physiologically safe at standard doses. Fatalities previously blamed on LSD toxicity were actually caused by overdoses, physical restraints, or other substituted drugs.

Keywords:
DeathHog-tyingLSDMaximal restraintPositional asphyxiationToxicity

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Area of Science:

  • Psychopharmacology
  • Toxicology
  • Forensic Medicine

Background:

  • Lysergic acid diethylamide (LSD) has a complex history, initially explored for psychiatric treatment but also associated with recreational use and adverse outcomes.
  • Physiological data indicate LSD is non-toxic and medically safe at standard dosages (50-200μg).
  • Recent reports have erroneously attributed five sudden deaths to "LSD toxicity".

Purpose of the Study:

  • To accurately identify the causes of fatalities previously misattributed to LSD toxicity.
  • To clarify the physiological safety profile of LSD in light of renewed therapeutic interest.

Main Methods:

  • Critical review of scientific literature and media reports concerning fatalities associated with LSD.
  • Analysis of case details to differentiate between LSD effects, overdoses, and other contributing factors.

Main Results:

  • Two of the five reported fatalities involved massive LSD overdoses.
  • Two deaths resulted from cardiovascular collapse in individuals subjected to excessive physical restraint after taking standard LSD doses.
  • One fatality was attributed to hyperthermia likely caused by a substituted drug (e.g., 25i-NBOMe), not LSD.

Conclusions:

  • Fatalities attributed to LSD toxicity are often mischaracterized.
  • True causes include massive overdoses, adverse events from physical restraints, and substitution with other potent psychoactive drugs.
  • Accurate understanding is crucial for evaluating the therapeutic potential of LSD and other psychedelics.