Edaravone protects against oxygen-glucose-serum deprivation/restoration-induced apoptosis in spinal cord astrocytes by inhibiting integrated stress response.

We previously found that oxygen-glucose-serum deprivation/restoration (OGSD/R) induces apoptosis of spinal cord astrocytes, possibly via caspase-12 and the integrated stress response, which involves protein kinase R-like endoplasmic reticulum kinase (PERK), eukaryotic initiation factor 2-alpha (eIF2α) and activating transcription factor 4 (ATF4). We hypothesized that edaravone, a low molecular weight, lipophilic free radical scavenger, would reduce OGSD/R-induced apoptosis of spinal cord astrocytes. To test this, we established primary cultures of rat astrocytes, and exposed them to 8 hours/6 hours of OGSD/R with or without edaravone (0.1, 1, 10, 100 µM) treatment. We found that 100 µM of edaravone significantly suppressed astrocyte apoptosis and inhibited the release of reactive oxygen species. It also inhibited the activation of caspase-12 and caspase-3, and reduced the expression of homologous CCAAT/enhancer binding protein, phosphorylated (p)-PERK, p-eIF2α, and ATF4. These results point to a new use of an established drug in the prevention of OGSD/R-mediated spinal cord astrocyte apoptosis via the integrated stress response.

[Electrophysiological and behavioral responses of male Apamea apameoides (Draudt) (Lepidoptera: Noctuidae) to sex pheromone components].

The sex pheromone gland extracts collected from calling females of Apamea apameoides (Lepidoptera: Noctuidae) were analyzed with GC-MS, the electrophysiological and behavioral responses of the male adults to serial dilutions of sex pheromone components and their synthetic blends were investigated with Y-tube olfactometer in laboratory and in bamboo forest field. The results indicated that (Z)-11-hexadecenyl acetate and (Z)-11-hexadecen-1-ol were the functional components in the sex pheromone gland extracts. Electroantennogram (EAG) recordings showed that sex pheromone gland extracts, (Z)-11-hexadecenyl acetate, (Z)-11-hexadecen-1-ol and the mixture of (Z)-11-hexadecenyl acetate and (Z)-11-hexadecen-1-ol all could elicit strong EAG responses, and the average EAG values increased with the increasing concentration of the sex pheromone. The blends of (Z)-11-hexadecenyl acetate and (Z)-11-hexadecen-1-ol at the ratio of 57:43 elicited a higher EAG value than each singular component did. The results of behavioral assay by Y-tube olfactometer accorded with those of EAG responses on the whole, and the mixture of (Z)-11-hexadecenyl acetate and (Z)-11-hexadecen-1-ol at the ratio of 57:43 was more attractive than each component alone. In field tests with silicone rubber as pheromone dispensers (concentration = 10(4) ng · uL(-1)), the average number of male adults captured per trap by the mixture was (48.5 ± 6.7).

[Calling and mating behaviors of bamboo shoot borer Kumasia kumaso].

The calling and mating behaviors of Kumasia kumaso were studied in laboratory at (25 1) degrees C and (60 +/- 10) % RH under a cycle 14 L:10 D photo period, and the EAG response of male K. kumaso to female K. kumaso sex gland extracts was also tested. The calling and mating behaviors of K. kumaso could only be observed in scotophase. The females began calling at the first scotophase following emergence, and the peak of calling occurred during the second scotophase and decreased thereafter. The calling of the females commenced 0-4 h after dark, reached the maximum between the 5th and the 7th hour of the scotophase, and terminated during the last 1-2.5 h of the scotophase. Moth age had significant effects on the calling patterns. With increasing moth age, the onset time of calling advanced gradually, and the mean number of calling bouts as well as the calling length per bout had a gradual increase from calling day 1 to day 4 but decreased on day 5. The peak time and terminated time of calling advanced with increasing moth age. The mating of K. kumaso adults initiated during the first scotophase and terminated till the 5th scotophase following emergence, and the peak of mating was observed during the second scotophase. The peak of mating was observed 5.5-7.0 h after dark, and advanced with increasing moth age. Moth age affected the mean onset time of mating and the copulation duration significantly. With increasing moth age, the mean onset time of mating advanced, and the copulation duration decreased. Sex ratio had significant effects on the mating behavior as well. Treatment 2 female:1 male showed a significantly higher mating percentage, but an earlier onset time of mating and shorter copulation duration, as compared with treatment 1 female:1 male. The results of EAG test indicated that the male adults showed a significant EAG response to the sex gland extracts of 2-day-old virgin females.