# Lysergic Acid Diethylamide (LSD) and the Heart: Exploring the Potential Impacts of LSD on Cardiovascular Function

**Authors:** Akshita Suleria, Sakshi Verma, Khanij Arya, Mason T Stoltzfus, Ira Gupta, Bhupinder Singh, Tanveer Shaik

PMC · DOI: 10.7759/cureus.87356 · Cureus · 2025-07-05

## TL;DR

This paper explores how LSD affects the heart, showing both potential risks and possible protective effects on cardiovascular health.

## Contribution

The paper introduces new insights into LSD's dual impact on cardiovascular function, linking micro-dosing to anti-inflammatory benefits.

## Key findings

- LSD can cause tachycardia and hypertension at acute doses, posing cardiovascular risks.
- Chronic LSD use may reduce atherosclerosis and thrombosis via 5-HT2A receptor antagonism.
- Micro-dosing LSD may lower chronic inflammation and improve synaptogenesis, benefiting heart health.

## Abstract

Lysergic acid diethylamide (LSD) is an ergot-derived psychedelic agent that produces perceptual and psychic effects of heightened sensations by acting on the dopaminergic, adrenergic, and serotonergic pathways in the brain and periphery, with 5-hydroxytryptamine 2A (5-HT2A) as the primary target molecule. Its action on these receptors in the central nervous system is comparatively well studied with respect to the psychedelic effects; however, there is speculative evidence of cardioprotective effects in the current literature attributed to the usage of this substance, even though acute ingestion causes tachycardia and hypertension, just like other psychedelics. Larger recreational doses of the drug can lead to cardiovascular and cerebrovascular incidents, but chronic peripheral antagonism of 5-HT2A receptors by the drug reduces atherosclerotic and thrombotic processes due to a reduction in platelet aggregation and vascular smooth muscle cell proliferation. Central sympathetic stimulation caused by micro-dosing of LSD imparts anti-inflammatory effects and increases cortical synaptogenesis, leading to reduced chronic inflammation implicated in causing cardiovascular diseases.

## Linked entities

- **Proteins:** HTR2A (5-hydroxytryptamine receptor 2A)
- **Chemicals:** Lysergic acid diethylamide (PubChem CID 5761), doxorubicin (PubChem CID 31703)
- **Diseases:** atherosclerosis (MONDO:0005311), thrombosis (MONDO:0000831)

## Full-text entities

- **Genes:** HTR2A (5-hydroxytryptamine receptor 2A) [NCBI Gene 3356] {aka 5-HT2A, HTR2}
- **Diseases:** inflammation (MESH:D007249), cardiovascular and cerebrovascular incidents (MESH:D002318), tachycardia (MESH:D013610), atherosclerotic (MESH:D050197), chronic (MESH:D002908), thrombotic (MESH:D013927), platelet aggregation (MESH:D001791), hypertension (MESH:D006973)
- **Chemicals:** LSD (MESH:D008238)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12322343/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12322343/full.md

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Source: https://tomesphere.com/paper/PMC12322343