Nystagmus duration after caloric irrigations.

Objective: To measure nystagmus duration after warm and cool caloric water irrigations, with the aim of providing preliminary evidence for the optimum interval between irrigation onsets; and to compare nystagmus durations between warm and cool irrigations, in addition to maximum slow phase velocity (SPV).Design: Participants underwent up to four caloric irrigations during routine appointments. Nystagmus was recorded to minimal levels (within 2°/s of subject's baseline). The nystagmus duration and maximum SPV were measured.Study Sample: 52 vestibular assessment patients (99 ears).Results: The mean nystagmus duration was 183.9 s (seconds) (3:04 min) from irrigation onset, and nystagmus became minimal after 264.8 s (4:25 min) in 97.5% of this sample. The population mean is within ±6.7 s of the sample mean (p = <0.001). There was no significant difference between warm and cool irrigation durations, and correlation and linear regression analysis showed duration cannot reliably be predicted by maximum SPV.Conclusions: Mean nystagmus duration (3 min after irrigation onset) and nystagmus duration for 97.5% of patients (<4.5 min) were substantially less than the BSA recommended 7 min between irrigations. These findings provide preliminary evidence for shortening of intervals between stimulus onsets, regardless of irrigation temperature or maximum SPV, to reduce caloric testing time and improve clinical efficiency.

Low-dose chronic prenatal alcohol exposure abolishes the pro-cognitive effects of angiotensin IV.

Prenatal ethanol exposure (PAE) in humans results in a spectrum of disorders including deficits in learning and memory. Animal models to date have typically used high ethanol doses but have not identified the biochemical changes underlying the cognitive deficit. This study used treatment of mouse breeding harems with 5% ethanol via drinking water throughout pregnancy and lactation and explored the behavioural consequences in the progeny at 3-6 months of age using the open field test, novel object recognition test and elevated plus maze to measure anxiety and memory consolidation. The effects of angiotensin IV on behaviour of the progeny were also determined. The results indicated that PAE increased anxiety-like behaviour as determined in the open field test in male but not female progeny. In control animals, angiotensin IV enhanced memory consolidation in males, but this effect was abolished by PAE. The abolition of the pro-cognitive effect of angiotensin IV was not a consequence of increased anxiety, and there was some evidence of a long-lasting anxiolytic effect of angiotensin IV in the male PAE progeny. These results suggest that PAE may act via alteration of the actions of the brain renin-angiotensin system to impair memory consolidation, but these effects may be partially sex-dependent.