Levonantradol Relieved One Morphine-Withdrawal Sign Without Suppressing the Syndrome in Monkeys

Levonantradol and nantradol alleviated abdominal contractions associated with morphine withdrawal in rhesus monkeys, but did not suppress the withdrawal syndrome overall. The same experiment also reported tolerance and negative findings in separate behavioral assays.

A symptom improvement was narrower than syndrome control

The cannabinoid-related compounds produced observable central nervous system depression. Neither suppressed morphine withdrawal, although both improved the chronic abdominal-contraction sign. Reporting only that improvement would overstate the result. Their directly observable effects were not antagonized by naloxone, further separating those observations from a simple claim of opioid-like action.

Tolerance and withdrawal were assessed separately

Repeated levonantradol administration produced marked tolerance to its own effects and cross-tolerance to nabilone and THC. Abrupt discontinuation did not produce observed withdrawal signs in the reported procedure. That null observation belongs to the tested regimen and observation method; it does not establish that every possible exposure lacks dependence potential.

Self-administration had its own comparator

When substituted for codeine in an intravenous self-administration procedure, neither compound maintained responding above vehicle rates. This was an operational animal test, not a human account of pleasure or craving. A negative result in that setup cannot establish a universal abuse-risk ranking for all cannabinoid compounds.

Interpreting the evidence

The study supports a selective withdrawal-sign finding alongside other positive and null outcomes. It does not establish human treatment efficacy or justify calling these experimental compounds equivalent to marijuana or opioid medicines.

Related reading: endogenous ligands administered as experimental drugs.

Research reference

Young AM; Katz JL; Woods JH (1981). Behavioral effects of levonantradol and nantradol in the rhesus monkey. Journal of clinical pharmacology. doi:10.1002/j.1552-4604.1981.tb02614.x. Evidence basis: study abstract.

Spread the love


The National Black Lawyers

top 40 lawyers

civil trial law

Lawyers of Distinction

Loading...

Recent Blog Articles

PEA Activated and Desensitized TRPV1 in Cells While Cannabinoid-Receptor Blockers Were Ineffective

A cell study linked palmitoylethanolamide effects to TRPV1 and PPAR-alpha rather than the tested cannabinoid receptors. Membership in a related lipid-signaling family did not establish CB1 or CB2 mediation of the measured response. The observations came from defined cell preparations Investigators measured intracellular calcium in differentiated F11 cells and examined…

Spread the love

Read Article: PEA Activated and Desensitized TRPV1 in Cells While Cannabinoid-Receptor Blockers Were Ineffective

CB1 Blockade Reduced NSAID Antinociception in a Rat Brain-Circuit Experiment

Blocking CB1 in the anterior cingulate cortex reduced the tested antinociceptive effects of NSAIDs in rats. Although the paper's title discusses tolerance, its supplied abstract describes acute drug-response findings, which should not be relabeled as proof of a tolerance-prevention intervention. The route targeted a particular brain region Investigators microinjected NSAIDs,…

Spread the love

Read Article: CB1 Blockade Reduced NSAID Antinociception in a Rat Brain-Circuit Experiment

Two Protective Preconditioning Methods Used Different Cannabinoid-Related Mechanisms in Rat Brain Slices

NMDA and DHPG preconditioning both reduced vulnerability to later injury in rat hippocampal slices, but CB1 blockade disrupted only the DHPG-related protection. Similar protective outcomes did not establish a shared mechanism. The preparation was an organotypic slice The investigators used rat hippocampal tissue and experimental excitotoxic or oxygen-and-glucose-deprivation insults. The…

Spread the love

Read Article: Two Protective Preconditioning Methods Used Different Cannabinoid-Related Mechanisms in Rat Brain Slices

Speak with an expert today!

Contact the offices of Okorie Okorocha for professional and reliable advice which you can trust.

Call (424) 363-3347 Contact Us