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1.
PLoS One ; 14(3): e0213781, 2019.
Article in English | MEDLINE | ID: mdl-30921346

ABSTRACT

During mammalian pregnancy and lactation, the maternal demand for calcium is increased to satisfy fetus and newborn skeletal growth. In addition to the dietary intake, females use the calcium contained in their bones to supply this increased demand, leading to a decrease in maternal bone mineral content. In reproductive insectivorous female bats, bone loss has been described as a physiological cost of reproduction, due to the reported increased risk of bone fracture. This physiological cost may be the mechanism underlying the conflict between increasing litter size and maintaining wing skeletal integrity, which would help to explain the small litter size of most bat species. If bone loss is a linking cost between reproduction and survival in bats, and most bat species have small litter sizes, one would expect to find a loss of bone and an increasing probability of bone fracture during pregnancy and lactation in other non-insectivorous bats. In this study, we tested for the existence of this cost in the Great-fruit eating bat, Artibeus lituratus. We analyzed trabecular structure, bone strength and bone mineral content for the humerus bone, hypothesizing that bone loss during reproduction in females would increase the risk of fracture. Our results showed a decrease of 22-31% in bone trabecular area in lactating females, rapidly compensated following weaning. Bone strength did not differ among reproductive and non-reproductive groups and seems to be more influenced by bone organic components rather than mineral contents. Since we observed bone loss during reproduction yet the humerus strength seems to be unaffected, we suggest that bone loss may not represent a physiological cost during reproduction for this frugivorous bat.


Subject(s)
Cancellous Bone/metabolism , Chiroptera/physiology , Reproduction/physiology , Animals , Body Weight , Bone Density , Cancellous Bone/chemistry , Cancellous Bone/pathology , Chiroptera/growth & development , Compressive Strength , Female , Lactation , Pregnancy
2.
Life Sci ; 152: 67-75, 2016 May 01.
Article in English | MEDLINE | ID: mdl-27009546

ABSTRACT

UNLABELLED: Wound healing involves a complex interaction between the cells, extracellular matrix and oxidative response. AIMS: Analyze the effects of 5α-Dihydrotestosterone (5α-DTH) ointment in cutaneous wound healing by secondary intention in diabetic Wistar rats. MAIN METHODS: Rats (302.23±26.23g, n=48) were maintained in cages with food and water ad libitum in accordance with the Guiding Principles in the Use of Animal Ethics Committee. Diabetes was induced by intraperitoneal injection of streptozotocin (60mg/kg). Three skin wounds (12mm diameter) were created on the animals' back, which were randomized into 6 groups according to the application received: VT group: Vehicle (lanolin), SA group: 0.9% saline solution, NC group: Non-diabetic, CP group: positive control (silver sulfadiazine 0001%), T1 group: Testosterone (10%), T2 group: Testosterone (20%) emulsified in lanolin. The applications were made daily within 21days, and tissues from different wounds were removed every 7days. KEY FINDINGS: Both groups treated with testosterone (T1 and T2) showed a significantly higher proportion of type I and type III collagen fibers. Superoxide dismutase levels were significantly higher on days 7 and 14 in testosterone treated groups. Protein carbonyls and MDA were lower in both groups. SIGNIFICANCE: We conclude that groups treated with 5α-DTH showed a better healing pattern with complete wound closure, and proved to have a positive effect on the morphology of the scar tissue as well as an antioxidant stimulating effect during secondhand intention skin wounds repair in diabetic rats.


Subject(s)
Diabetes Mellitus, Experimental/complications , Dihydrotestosterone/pharmacology , Wound Healing/drug effects , Animals , Antioxidants/pharmacology , Cicatrix/pathology , Collagen Type I/metabolism , Collagen Type III/metabolism , Dihydrotestosterone/therapeutic use , Drug Compounding , Male , Mast Cells/drug effects , Protein Carbonylation/drug effects , Rats , Rats, Wistar , Skin/injuries
3.
J Anat ; 222(3): 372-9, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23305159

ABSTRACT

Knowledge of the stages that compose the seminiferous epithelium cycle (SEC) and determination of the duration of spermatogenic processes are fundamental for the accurate quantification of the dynamics of spermatogenesis. The aim of this study was to characterize the stages that compose the SEC of the bat Sturnira lilium, including evaluation of the average frequency of each of these stages throughout the year and calculation of the duration of the spermatogenic process. An ultrastructural characterization of the formation of the acrosomal cap was also performed. Testicular fragments were processed for morphological and immunohistochemical analysis as well as ultrastructural analysis using transmission electron microscopy. According to the tubular morphology method, the SEC in S. lilium is divided into eight stages, following the pattern found in other mammals. Primary spermatocytes were found at zygotene in stage 1 of the cycle. There was no variation in frequency of each of the stages over the seasons, with stage 1 being the most frequent, and stage 7 the least frequent. The duration of one seminiferous epithelium cycle was 3.45 days, and approximately 15.52 days were required for the development of sperm from spermatogonia. Ultrastructural characterization allowed the formation of the acrosomal cap in round spermatids to be monitored. In conclusion, the stages that compose the SEC in S. lilium are generally similar to those described for other mammals, but the duration of the spermatogenic process is shorter than previously recorded for mammals. The presence of primary spermatocytes at zygotene in stage 1 of the cycle is probably due to the longer duration of this stage.


Subject(s)
Chiroptera/physiology , Seminiferous Epithelium/physiology , Acrosome/ultrastructure , Animals , Male , Microscopy, Electron, Transmission , Seminiferous Epithelium/cytology , Seminiferous Tubules/anatomy & histology , Seminiferous Tubules/physiology , Spermatocytes/cytology , Testis/anatomy & histology
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