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Teratologic effects of LSD in explanted early chick embryos
Teratology
|April 1, 1975
Summary
Lysergic acid diethylamide (LSD) exposure during early chick embryo development caused axial structure abnormalities and reduced heart rate. However, these developmental effects were reversible upon removal from LSD.
Area of Science:
- Developmental biology
- Pharmacology
- Teratology
Background:
- Lysergic acid diethylamide (LSD) is a potent psychoactive substance.
- Understanding the impact of teratogens on early embryonic development is crucial for public health.
- The effects of LSD on embryonic development are not well-documented.
Purpose of the Study:
- To investigate the teratogenic effects of LSD on early chick embryo development.
- To determine the dose-dependent effects of LSD on embryonic morphogenesis and physiology.
- To assess the reversibility of LSD-induced developmental abnormalities.
Main Methods:
- Chick embryos at stages 4-7 were explanted and cultured for 20 hours.
- Embryos were exposed to varying concentrations of LSD (≥10 µg/ml).
- Morphological and physiological parameters, including axial structures, somites, heart development, pulse rate, cell morphology, and mitotic activity, were assessed.
Main Results:
- LSD exposure (≥10 µg/ml) induced abnormalities in axial structures, particularly somites, in over 50% of embryos.
- LSD significantly lowered embryonic pulse rate but did not affect heart morphogenesis.
- Cellular degeneration was observed in severely affected structures, but LSD did not alter cell morphology or mitotic activity.
- Embryos exposed to LSD for 4-5 hours retained the ability to undergo normal morphogenesis upon subculturing on a plain medium, indicating reversibility.
Conclusions:
- LSD exhibits teratogenic potential, primarily affecting axial development and cardiac function in early chick embryos.
- The observed developmental abnormalities induced by LSD are reversible, suggesting a transient impact on developmental processes.
- This study highlights the importance of avoiding teratogenic substance exposure during critical developmental windows.