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Male Rhesus Monkey (male + rhesus_monkey)
Selected AbstractsAbsence of corneal endothelium injury in non-human primates treated with and without ophthalmologic drugs and exposed to 2.8,GHz pulsed microwaves,,BIOELECTROMAGNETICS, Issue 4 2010Shin-Tsu Lu Abstract Microwave-induced corneal endothelial damage was reported to have a low threshold (2.6,W/kg), and vasoactive ophthalmologic medications lowered the threshold by a factor of 10,0.26,W/kg. In an attempt to confirm these observations, four adult male Rhesus monkeys (Macaca mulatta) under propofol anesthesia were exposed to pulsed microwaves in the far field of a 2.8,GHz signal (1.43,±,0.06,µs pulse width, 34,Hz pulse repetition frequency, 13.0,mW/cm2 spatial and temporal average, and 464,W/cm2 spatial and temporal peak (291,W/cm2 square wave equivalent) power densities). Corneal-specific absorption rate was 5.07,W/kg (0.39,W/kg/mW/cm2). The exposure resulted in a 1.0,1.2,°C increase in eyelid temperature. In Experiment I, exposures were 4,h/day, 3 days/week for 3 weeks (nine exposures and 36,h total). In Experiment II, these subjects were pretreated with 0.5% Timolol maleate and 0.005% Xalatan® followed by 3 or 7 4-h pulsed microwave exposures. Under ketamine,xylazine anesthesia, a non-contact specular microscope was used to obtain corneal endothelium images, corneal endothelial cell density, and pachymetry at the center and four peripheral areas of the cornea. Ophthalmologic measurements were done before and 7, 30, 90, and 180 days after exposures. Pulsed microwave exposure did not cause alterations in corneal endothelial cell density and corneal thickness with or without ophthalmologic drugs. Therefore, previously reported changes in the cornea exposed to pulsed microwaves were not confirmed at exposure levels that are more than an order of magnitude higher. Bioelectromagnetics 31:324,333, 2010. Published 2010 Wiley-Liss, Inc. [source] Agnathia and associated malformations in a male rhesus monkeyJOURNAL OF MEDICAL PRIMATOLOGY, Issue 4 2008B. Goldschmidt Abstract Background, Agnathia is a rare malformation characterized by the absence of the mandible. Methods, A male rhesus monkey with malformations was found dead and studied by internal examination, radiographs and histopathology. Results, A case of a rare first branchial arch anomaly with agenesis of the mandible and tongue is presented. The animal also had visceral deformities. However, ears were normal in shape and only slightly low in position. The craniofacial malformations may reflect incomplete separation of the first branchial arch into its maxillary and mandibular processes. Conclusions, The association between the craniofacial and other corporal anomalies is unclear. [source] Depo-Provera abrogates attenuated lentivirus-induced protection in male rhesus macaques challenged intravenously with pathogenic SIVmac239JOURNAL OF MEDICAL PRIMATOLOGY, Issue 4-5 2007Meritxell Genescą Abstract Background, Progesterone administration prior to intravaginal challenge with pathogenic SIVmac239 decreases the protective efficacy of live attenuated vaccines in rhesus macaques. Methods, To determine if progesterone alters the efficacy of live attenuated vaccines through local or systemic effects, seven male rhesus macaques were immunized with SHIV89.6 and then challenged intravenously with SIVmac239. Three of these animals were treated with Depo-Provera 30 days prior to the SIV challenge. Results, The SHIV animals had significantly lower plasma viral RNA levels than the unimmunized control monkeys, but the Depo-Provera treated, SHIV-immunized animals did not. Despite the lack of protection, the Depo-Provera SHIV animals had strong SIV specific T-cell responses. However, altered patterns of NK frequency and CD38 T-cell expression prior to SIV challenge were observed in Depo-Provera SHIV animals. Conclusions, Depo-Provera eliminates live-attenuated lentivirus vaccine efficacy in male rhesus monkeys through systemic effects on antiviral immunity and/or viral replication. [source] The Effects of Ethanol Consumption on Vasculogenesis Potential in Nonhuman PrimatesALCOHOLISM, Issue 1 2008J. Koudy Williams Background:, Vasculogenesis is essential to the preservation and repair of damaged or diseased vessels. Alcohol is the most commonly abused drug among young adults, but its effects on vessel growth and repair are unknown. The basis of vascular repair is endothelial progenitor cell (EPC) recruitment to assist in the formation of new vascular network (vasculogenesis). Therefore, the objective of this study was to measure the effects of ethanol consumption on the production, mobilization and vasculogenesis potential EPCs in nonhuman primates. Methods:, Four to five year-old (young adult) male rhesus monkeys consumed monkey chow and water (Control, n = 7), or chow and water + ethanol (Alcohol, 2.45 g/d, n = 7) for 12 months. Peripheral blood (PB) and bone marrow (BM) samples were collected for fluorescence-activated cell-sorting analysis of cell surface antigens (CD45, CD31, CD44, CD133, VEGF-R2 , or KDR); and for capillary formation on Matrigel-coated plates. Results:, There were greater numbers of nonhematopoeitic stromal cells (CD45,) and putative mesenchymal progenitor cells (CD45,/CD44+) in the PB and BM of Alcohol versus Control monkeys (p < 0.05). Additionally, there were greater numbers of EPCs (CD45,/CD133+/KDR+) in the BM and PB of Alcohol versus Control monkeys (p < 0.05). However, the EPCs of Alcohol monkeys were less likely to form capillaries on matrigel-coated plates than Control monkeys (p < 0.05). Conclusions:, Ethanol consumption in monkeys markedly increased the production and mobilization of EPCs, but decreased their ability to form capillaries. The pathophysiologic consequences of such effects are unclear, but may represent an ethanol-induced chronic stress on the BM, resulting in EPC. [source] | ||||||||||