This study aimed to examine the effect of a mild elevation in serum cholesterol level in a porcine coronary overstretch restenosis model using a balloon angioplasty catheter or drug-eluting coronary stent. Pigs were divided into two groups and were fed a commercial normal diet (CND, n = 4) or a high-fat diet (HFD, n = 4) for 5 weeks. Coronary overstretch injury by balloon angioplasty or stent implantation was induced in the left anterior descending and left circumflex artery after 1 week of feeding. Histopathological analysis was performed at 4 weeks after coronary injury. During the experiment, the total cholesterol level in the HFD group increased by approximately 44.9% (from 65.9 ± 3.21 mg/dL at baseline to 95.5 ± 9.94 mg/dL at 5 weeks). The lumen area in the CND group was reduced in comparison with that in the HFD group after balloon angioplasty. After stent implantation, the injury score showed no significant difference. There were significant differences in the neointimal area (2.7 ± 0.33 mm2 in the CND group vs. 3.3 ± 0.34 mm2 in the HFD group, p<0.05), lumen area (2.6 ± 0.54 mm2 in the CND group vs. 2.0 ± 0.33 mm2 in the HFD group, p<0.05), and percent area stenosis (52.0 ± 7.96% in the CND group vs. 62.4 ± 5.15% in the HFD group, p<0.05). Body weight change was not different between the two groups. Increased serum cholesterol level activated vascular smooth muscle cell proliferation in the porcine coronary overstretch model.

Defended (distasteful or toxic) prey are often characterized by conspicuous coloration and this phenomenon is called "aposematism". The main advantage of aposematism is that it promotes faster learning by predators to avoid the prey. Some defended prey species use a different strategy; they remain cryptic in the normal state, but display conspicuous aposematic signal (which is normally hidden) in response to a predator's approach/attack. This anti-predator strategy of a defended prey has not been well studied yet although it can theoretically give the benefits of both camouflage and aposematism. Here, we investigated the effectiveness of this ‘hidden-aposematic signal’ as a warning signal. Using wild tits (Parus minor) as predator and novel artificial prey models (which mimics wings of insects), we tested whether hidden conspicuous signal of a defended prey enhances the avoidance learning rate of predators and how does it compare with the typical conspicuous/non-conspicuous signal. We found that hidden conspicuous signal indeed enhances the avoidance learning rate of predators in comparison with the non-conspicuous signal. However the overall learning rate by predators to avoid the defended prey was slower than for the normal conspicuous signal. Our results suggest that the prey with hidden-aposematic signals could enjoy both the benefits camouflage and the benefits of aposematism that are however lower than benefits from a typical aposematic signal. We, for the first time, highlight the functional aspect of a unique, but yet largely ignored, defensive coloration of prey.

Cryptic color patterns in prey are classical examples of adaptations to avoid predation, but we still know little about behaviors that reinforce the match between animal body and the background. For example, moths avoid predators by matching their color patterns with the background, but the contribution of their behavior to their crypticity have not been well understood. Here, we report the previously underappreciated ability of moths to find the locally most cryptic spot and body orientation by using two species Hypomecis roboraria and Jankowskia fuscaria. We show that body positioning behavior, performed frequently by moths after landing on bark, results in a significant increase of the camouflage effect provided by their cryptic color pattern alone. We also found that moths recognize multiple background cues, such as furrow structure, visual patterns, and roundness to position and orient themselves. Our study demonstrate morphological adaptations, such as color pattern of moths, cannot be fully understood without taking into account a behavioral phenotype that coevolved with the morphology for increasing the adaptive value of the morphological trait.