Anna Holmes

Acute nicotine enhances strategy-based semantic processing in Parkinson's disease

Nicotinic mechanisms may play a role in the cognitive deficits of Parkinsons disease (PD). Recently, on a cognitively demanding strategy-based priming task, nicotine selectively affected controlled semantic processing in young adult non-smokers as reported by Holmes et al. (International Journal of Neuropsychopharmacology 11, 389-399, 2008). Such controlled semantic processing is compromised in PD. This study investigated the effects of acute transdermal nicotine on controlled semantic processing in non-smokers with PD (n = 10) and non-smoking matched controls (n = 16) using a strategy-based semantic priming paradigm. Transdermal nicotine patches (7 mg/24 h) were administered in a double-blind, placebo-controlled, crossover design. Participants were instructed to expect target words from specified semantic categories based on the primes, while unexpected targets were also presented. Priming conditions included those concurring with trained expectations (expected-related and expected-unrelated), those which did not (unexpected-related and unexpected-unrelated), and neutral-baseline conditions. Controls evidenced significant expectancy effects (i.e. reaction-time differences for expected vs. unexpected conditions) under both drug states. An expectancy effect was not evident for PD under placebo due to a lack of reaction-time slowing for unexpected conditions. However, under nicotine an expectancy effect was present for PD at a level comparable to controls. Overall the findings indicate that nicotine can improve impaired controlled semantic processing in PD possibly via enhanced expectancy or inhibitory mechanisms.

Transdermal nicotine modulates strategy-based attentional semantic processing in non-smokers.

Nicotine has been shown to improve various aspects of cognitive processing such as attention and memory, however, its effects on lexical-semantic processing are relatively uncharted. Recent investigations of mnemonic processing in minimally deprived smokers suggest that nicotine might selectively modulate processes concerned with associative memory. This study investigated the effects of nicotine on lexical-semantic processing in non-smokers using a strategy-based lexical-decision priming paradigm. Transdermal nicotine patches (7 mg/24 h) were administered within a double-blind, placebo-controlled, cross-over design. Participants were trained to expect target words to come from a specified semantic category based on the prime word, although in some instances trained expectations were not met. Participants were presented with the stimuli at either a short or long stimulus onset asynchrony (SOA) to target automatic and attentional processing, respectively (n=12 and 17 for the short and long SOAs, respectively). Nicotine was found to selectively affect priming condition reaction times at the long SOA, indicating a nicotinic modulation of attentional mechanisms. Specifically, facilitation effects were dominant under placebo compared to a dominance of inhibition effects under nicotine. These results suggest that nicotine supports inhibitory attentional mechanisms in cognitively demanding semantic processing paradigms.

Nicotine effects on general semantic priming in Parkinson’s disease

In young healthy nonsmokers, effects of nicotine on semantic processing have been observed under strategy-based priming procedures but not under more general priming procedures (Holmes, Chenery, & Copland, 2008; Holmes, Chenery, & Copland, 2010). Effects of nicotine under general priming procedures, however, may be mediated by baseline priming levels that are below optimum such as when compromised by disease. Nicotinic mechanisms may be involved in the cognitive sequalae of Parkinsons disease (PD). Evidence suggests that semantic processing may be compromised in PD but the potential benefit of nicotinic stimulation is unknown. This study investigated the effects of nicotine on semantic processing in nonsmokers with PD (n = 12) and nonsmoking matched controls (n = 17) using general priming procedures. Specifically, an automatic priming task (0.15 relatedness proportion, RP, and 200 ms stimulus onset asynchrony, SOA) and a controlled priming task (0.8 RP and 1000 ms SOA) were used. Prime-target category relation (category related, noncategory related) was also manipulated. Transdermal nicotine patches (7 mg/24 h) were administered in a double-blind, placebo-controlled, crossover design. For the automatic task, nicotine did not influence priming effects for PD. Unexpectedly, compromised automatic priming for controls was ameliorated. For the controlled task, nicotine influenced priming effects for PD but not controls. The patterns of priming and nicotine effects across the tasks suggest an age-related slowing of the rate of semantic activation for controls, which may be exacerbated in PD. Overall, the findings indicate that nicotine can improve compromised semantic processing in PD, and also influence semantic processing in healthy older individuals.

Neural Substrates of Naming Following Semantic Verification in Aphasia

Semantic verification tasks can facilitate naming in healthy and aphasic individuals, however, the neurocognitive mechanisms involved are unclear, This study examined the neural mechanisms underpinning short and long-term semantic facilitation of naming in two individuals with anomia.