Vasoactive intestinal polypeptide in rat heart atria: the effect of hyperthyroidism

Citation
J. Kuncova et J. Slavikova, Vasoactive intestinal polypeptide in rat heart atria: the effect of hyperthyroidism, PHYSL RES, 49(4), 2000, pp. 427-434
Citations number
42
Categorie Soggetti
Physiology
Journal title
PHYSIOLOGICAL RESEARCH
ISSN journal
08628408 → ACNP
Volume
49
Issue
4
Year of publication
2000
Pages
427 - 434
Database
ISI
SICI code
0862-8408(2000)49:4<427:VIPIRH>2.0.ZU;2-3
Abstract
The effects of transient and sustained hyperthyroidism on vasoactive intest inal polypeptide-like immunoreactivity (VIP-LI) levels were studied in the heart atria of developing and adult rats. Newborn rats were divided into 5 groups. Neo-T animals were treated with thyroxine (T4) during postnatal day s 1-8 and sacrificed at the age of 60 days. Neo-S rats were treated with T4 during postnatal days 1-60 and sacrificed one day later. Adult-1 and Adult -2 animals received T4 during days 52-60 and were sacrificed 5-6 days and 1 day later, respectively. Control animals were injected with saline. VIP-LI concentrations were determined in extracts from the left and right atria s eparately. In Neo-S and Adult-2 rats, spontaneous heart rate, the weight of both atria and total T4 serum levels were significantly enhanced, while th eir body weight was decreased. The ratio atria weight to body weight was si gnificantly increased in ail groups except for Adult-1 animals. Hyperthyroi dism led to a significant decrease in VIP-LI levels in both atria of Neo-S and Neo-T rats. Hyperthyroidism induced in adult rats also decreased VIP-LI levels in both atria. However, this change was only transient. In conclusi on, our data have provided new evidence that hyperthyroidism induced during the early neonatal period interferes with the development of VIP-ergic inn ervation in rat atria. The period of the first few postnatal days seems to be essential for this effect, since VIP-LI concentrations in 60-day-old ani mals did not significantly differ between Neo-S and Neo-T atria.