Simple SummaryFecal glucocorticoid metabolite (fGCM) concentrations were examined in captive Asian elephants in relation to sex, body condition score, and working conditions. A total of 870 samples from 37 elephants in four elephant facilities were collected. We used a cortisol enzyme immunoassay for quantification of fGCM concentrations in fecal samples. Mean fGCM varied significantly across elephant facilities. Female elephants born in the wild exhibited elevated fGCM concentrations across all the facilities compared to males and captive-born elephants.AbstractAsian elephant (Elephas maximus) populations, both in the wild and in captivity, have been continually declining over the decades. The present study examined the physiological stress response of captive Asian elephants in relation to body condition score and different working conditions. A total of 870 dung samples of 37 captive elephants (24 males and 13 females) from four facilities were collected to examine fecal glucocorticoid metabolite concentrations (fGCM). The elephants in forest camps with exposure to natural habitats had a higher body condition score than those in more confined spaces. Wild born elephants and females (except in one case) had higher concentrations of fGCM than captive born elephants and males, respectively. Elephants engaged in the Dussehra festival had elevated fGCM concentrations than their counterparts at Mysore zoo. We recommend a few management practices for the long-term survival of rapidly declining captive elephant populations.
The study aimed to investigate whether a 3D printed beta-tricalcium phosphate (β-TCP) scaffold tethered with growth factors and fibrin glue implanted autologous bone marrow-derived mesenchymal stem cells would provide a 3D platform for bone regeneration resulting in new bone formation with plasticity. Twenty 3D printed β-TCP scaffolds, ten scaffolds engrained with osteogenic mesenchymal stem cells with fibrin glue (group A), and ten scaffolds used as a control group with β-TCP scaffold and fibrin glue inoculation only (group B) were included in the study. Cell infiltration, migration, and proliferation of human osteogenic stem cells on the scaffolds were executed under both static and dynamic culture conditions. Each scaffold was examined post culture after repeated changes in the nutrient medium at 2, 4 or 8 weeks and assessed for opacity and formation of any bone-like tissues macroscopic, radiographic, and microscopic evaluation. Significant changes in all the prerequisite parameters compiled with an evaluated difference of significance showing maxillofacial skeletal repair via tissue engineering by β-TCP scaffold and MSCs remains will be the most promising alternative to autologous bone grafts and numerous modalities involving a variety of stem cells, growth factors from platelet-rich fibrin.
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