Fine structure of lymphoid cells in the nasal skin of primates.

Electron microscopy of the nasal skin of primates shows that lymphoid cells are normally present in this region. No degeneration or mitosis of these cells or their transformation into other cell types was seen. These intraepidermal lymphocytes contained cytoplasmic fibrils. There was no evidence that they were phagocytic in the epidermis. The present study suggests that these lymphoid cells migrate into the lamina propria but not into the epidermis.     

Estimation of density of gibbon groups by use of loud songs

The density of gibbon populations may be estimated by listening for the loud duetted songs of monogamous territorial groups. This method requires a correction factor which must be estimated from the frequency of singing of an adequate number of known study groups. The correction factor and its error were estimated for pileated gibbons (Hylobates pileatus) in Khao Soi Dao Wildlife Sanctuary in southeastern Thailand. Among 30 groups studied, 47% sang per day, on average, but the variation between days and the variation in singing frequency between groups were large. Weather conditions, especially windiness, explained some variation in singing. During an area-wide survey of groups in the sanctuary, unexplained variation in singing from day to day accounted for approximately half of the sample error of group density estimated from 1-day listening samples. Error due to day-to-day variability can be reduced by listening for more than one day at each site. Correction factors based on the cumulative proportion of groups heard during longer (2–5-day) sample periods of listening were closer to 1.0, therefore leaving less room for error and bias of the correction factor. © 1993 Wiley-Liss, Inc.     

Global versus Local Changes in Upwelling Systems (Collection Colloques et séminaires)

Reviews in Fish Biology and Fisheries -     

Escitalopram oxalate induces apoptosis in U‐87MG cells and autophagy in GBM8401 cells

Glioblastoma multiforme (GBM) is recognized as a most aggressive brain cancer with the worst prognosis and survival time. Owing to the anatomic location of gliomas, surgically removing the tumour is very difficult and avoiding damage to vital brain regions during radiotherapy is impossible. Therefore, therapeutic strategies for malignant glioma must urgently be improved. Recent studies have demonstrated that selective serotonin reuptake inhibitors (SSRIs) have cytotoxic effect on certain cancers. Considering as a more superior SSRI, escitalopram oxalate exhibits favourable tolerability and causes generally mild and temporary adverse events. However, limited information is revealed about the influence of escitalopram oxalate on GBM. Therefore, an attempt was made herein to explore the effects of escitalopram oxalate on GBM. The experimental results revealed that escitalopram oxalate significantly inhibits the proliferation and invasive ability of U‐87MG cells and significantly reduced the expressions of cell cycle inhibitors such as Skp2, P57, P21 and P27. Notably, escitalopram oxalate also induced significant apoptotic cascades in U‐87MG cells and autophagy in GBM8401 cells. An animal study indicated that escitalopram oxalate inhibits the proliferation of xenografted glioblastoma in BALB/c nude mice. These findings implied that escitalopram oxalate may have potential in treatment of glioblastomas.