L-name, a nitric oxide synthase inhibitor, as a potential countermeasure to post-suspension hypotension in rats

Citation
Ma. Bayorh et al., L-name, a nitric oxide synthase inhibitor, as a potential countermeasure to post-suspension hypotension in rats, CLIN EXP HY, 23(8), 2001, pp. 611-622
Citations number
28
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
CLINICAL AND EXPERIMENTAL HYPERTENSION
ISSN journal
10641963 → ACNP
Volume
23
Issue
8
Year of publication
2001
Pages
611 - 622
Database
ISI
SICI code
1064-1963(200111)23:8<611:LANOSI>2.0.ZU;2-8
Abstract
A large number of astronauts returning from spaceflight experience orthosta tic hypotension. This hypotension may be due to overproduction of vasodilat ory mediators, such as nitric oxide (NO) and prostaglandins. To evaluate th e role of the NO synthase inhibitor N-G-nitro-L-arginine methyl ester (L-NA ME) as a countermeasure against the post-suspension reduction in mean arter ial pressure (MAP), we assessed the cardiovascular responses and vascular r eactivity to 7-day 30 degrees tail-suspension and a subsequent 6 hr post-su spension period in conscious rats. After a pre-suspension reading, direct M AP and heart rate (HR) were measured daily and every 2 hrs post-suspension. The NO synthase. inhibitor L-NAME (20 mg/kg, i.v.), or saline, were admini stered after the 7(th) day reading prior to release from suspension and at 2 and 4 hrs post-suspension. At 6 hrs post-suspension, vascular reactivity was assessed. While MAP did not change during the suspension period, it was reduced post-suspension. Heart rate was not significantly altered. L-NAME administration reversed the post-suspension reduction in MAP. In addition, the baroreflex sensitivity for heart rate was modified by L-NAME. Thus, the post-suspension reduction in MAP may be due to overproduction of NO and al tered baroreflex activity.