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Studies on the goiter inhibiting action of iodolactones
M A Pisarev1, L Krawiec, G J Juvenal
1División Bioquímica Nuclear, Gerencia de Radiosótopos y Radiaciones, Comisión Nacional de Energía Atómica, Buenos Aires, Argentina.
Abstract:
The thyroid gland synthesizes 6-delta-iodolactone, a compound shown to inhibit goiter growth in vivo and cell proliferation in culture. The present studies were performed to characterize this effect further with the aim of exploring the possible therapeutic action of iodolactones. Prevention assay: rats were treated simultaneously with a goitrogen, methylmercaptoimidazole, and either 6-delta-iodo-lactone or 14-iodo-omega-lactone, a synthetic derivative, given either i.p. or p. o. Both compounds caused a significant decrease in thyroid weight irrespective of the route of administration, but oral administration was less effective. A dose-response relationship was observed, the minimal effective dose (i.p.) being 3 micrograms/day. Involution assay: goiter was first induced with methylmercaptoimidazole and then the iodolactones were injected. Both compounds caused a significant involution, which was dose-related. Acute (10 days) administration of the iodolactones did not produce significant changes in several serum parameters (total T3 and T4, cholesterol, total protein, urea and acetylcholinesterase). These results give further support to the potential therapeutic application of iodolactones.
Insights
Iodolactones, compounds synthesized by the thyroid gland, effectively inhibit goiter growth and cell proliferation. These findings suggest potential therapeutic applications for iodolactones in treating thyroid conditions.
Area of Science:
- Endocrinology
- Molecular Biology
- Pharmacology
Background:
- The thyroid gland produces 6-delta-iodolactone, a compound known to inhibit goiter growth and cell proliferation.
- Further characterization of iodolactones is needed to explore their therapeutic potential.
Purpose of the Study:
- To further characterize the goiter-inhibiting effects of 6-delta-iodolactone and its synthetic derivative, 14-iodo-omega-lactone.
- To investigate the therapeutic potential of iodolactones.
Main Methods:
- Prevention assay: Rats were co-administered a goitrogen (methylmercaptoimidazole) with either 6-delta-iodolactone or 14-iodo-omega-lactone via intraperitoneal (i.p.) or oral (p.o.) routes.
- Involution assay: Goiter was induced in rats, followed by injection of iodolactones.
- Serum parameters (T3, T4, cholesterol, protein, urea, acetylcholinesterase) were analyzed after acute iodolactone administration.
Main Results:
- Both iodolactones significantly decreased thyroid weight in the prevention assay, with i.p. administration being more effective than p.o.
- A dose-response relationship was observed, with a minimal effective i.p. dose of 3 micrograms/day.
- Significant, dose-related goiter involution was observed in the involution assay.
- Acute iodolactone administration did not significantly alter key serum parameters.
Conclusions:
- Iodolactones demonstrate significant efficacy in both preventing and reversing goiter in vivo.
- The observed dose-dependent effects and lack of adverse effects on serum parameters support the potential therapeutic application of iodolactones for thyroid disorders.
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Goiter

