Abstract
Nitric oxide (NO)-mediated angiogenesis may play a role in establishing dense retinal vasculatures of Antarctic hemoglobinless icefishes (suborder: Notothenioidei). We hypothesized that loss of hemoglobin (Hb) leads to elevation in [NO] due to decreased degradation of the compound when the NO-scavenger Hb is absent, thereby inducing vascular growth. We found that total mass of NO metabolites, nitrite plus nitrate (NOx), in plasma is greater in icefishes than in red-blooded notothenioids [e.g. C. aceratus (Hb−), 22.7±2.9μM; N. coriiceps (Hb+), 14.7±1.7μM], suggesting a higher NO load in hemoglobinless animals. High NO levels do not appear to be a result of greater NO synthesis; we consistently measured lower activities of the enzyme catalyzing NO production, nitric oxide synthase, in tissues of icefishes than in Hb-expressing notothenioids [e.g. 96±10 and 216±39 pmol(min g wet wt)−1 in brain tissue of C. aceratus (Hb−) and G. gibberifrons (Hb+), respectively]. Levels of mRNA for hypoxia-induced (HIF-1α and PHD2) and angiogenic genes (VEGF) were similar in red- and white-blooded species, indicating that vascular maintenance in adult animals does not require differences in angiogenic tone. This does not preclude a cause-and-effect relationship between absence of Hb and NO-mediated angiogenesis during earlier ontogenetic stages of icefishes.
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More From: Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology
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