219 MORPHOMETRIC CHARACTERIZATION OF EPIDIDYMAL AND EJACULATED SPERMATOZOA FROM BROWN BEAR (URSUS ARCTOS)

2006 ◽  
Vol 18 (2) ◽  
pp. 217 ◽  
Author(s):  
V. Garcia-Macias ◽  
F. Martinez-Pastor ◽  
M. Alvarez ◽  
P. Paz ◽  
S. Borragan ◽  
...  

Sperm morphology is an useful characteristic for estimating potential fertility. Currently, we are obtaining baseline information on various aspects of reproduction in the brown bear (Ursus arctos) with the intention of using the knowledge to establish a germplasm bank for the species. In the present report, we describe the results obtained using assisted sperm morphology analysis (ASMA, Sperm Class Analyzer®; Microptic S.L, Barcelona, Spain) to analyze the morphological differences in epidydimal (caput, corpus, and cauda) and ejaculated brown bear spermatozoa. A post-mortem epididymal sperm sample was obtained from an adult brown bear after accidental death. The epididymides were excised, washed, and dissected into the three major segments; caput, corpus and cauda. Then multiple incisions were made in the tissue to allow migration of spermatozoa into the surrounding medium. Semen was collected by electroejaculation from five adult brown bears living in a semi-free ranging environment in the Cabarceno Park (Cantabria, Spain). Anesthesia was induced using tiletamine + zolazepan (Zoletil 100®; Virbac, Carras, France; 7 mg/kg), and ketamine (Imalgene 1000®; Rhone Merieux, Lyon, France; 2 mg/kg). The electroejaculation unit (PT Electronics®; Boring, Oregon) was connected to a 3-lateral electrode transrectal probe (26 mm in diameter, 320 mm in length). Ejaculation occurred at 6–10 V/250–300 mA. For head morphometry assessment, sperm samples were fixed in glutaraldehyde and slides were smeared and air-dried for 2 h. The samples were then stained with Diff-Quik® staining (37°C; 10 min in the red component and 15 min in the blue component). The area, perimeter, length and width, and ellipticity (length/width) of heads were measured from at least 100 spermatozoa/slide. As shown in Table 1, values obtained for each measure were similar in both epididymal and ejaculated spermatozoa. These results provide normal morphometry values for brown bear spermatozoa, a potentially useful characteristic for predicting fertility. Table 1. Head morphometry for epididymis and ejaculated bear sperm (mean ± SD) This work was supported in part by CANTUR S.A. and CICYT (CGL 2004–0278/BOS).

2005 ◽  
Vol 41 (2) ◽  
pp. 298-303 ◽  
Author(s):  
Torsten Mörner ◽  
Hanna Eriksson ◽  
Caroline Bröjer ◽  
Kristina Nilsson ◽  
Henrik Uhlhorn ◽  
...  

2007 ◽  
Vol 19 (1) ◽  
pp. 237 ◽  
Author(s):  
L. Anel ◽  
V. Garcia-Macias ◽  
F. Martinez-Pastor ◽  
M. Alvarez ◽  
S. Borragan ◽  
...  

Having recently observed that survival of red deer spermatozoa after cryopreservation seemed to reflect the size of sperm heads, we hypothesized that cryoresistance of brown bear spermatozoa might also be dependent on head size, since in a preliminary study we had also observed significant differences in sperm head sizes among male brown bears (median values for area 22.2 �m2, perimeter 18.2, length 6.1 and width 4.4 �m). In the present report, we analyzed the post-thaw survival of spermatozoa of 6 brown bears that were assigned to 2 groups (3 bears/group) based on sperm size: Group A with large-size sperm heads; Group B with small-size heads. Ejaculates were obtained by electroejaculation of adult brown bears (semi-free ranging in Cabarceno Park, Cantabria, Spain) under general anesthesia (7 mg kg-1 tiletamine + zolazepan and 2 mg kg-1 ketamine). Semen was diluted (Tes-Tris-fructose, 8% glycerol, 20% egg yolk, EDTA, and Equex paste), loaded in 0.25-mL straws, and frozen in a biofreezer at 20�C min-1 to -100�C. After storage in liquid nitrogen, samples were thawed in water at 65�C for 6 s and survival was measured. Sperm motility (TM: total, and PM: progressive; %) was assessed microscopically, and sperm viability, acrosome integrity (PI/PNA-FITC), and mitochondrial status (JC-1) were assayed for fresh and thawed sperm by flow cytometry. Recovery rates (RR: thawed/fresh � 100) were calculated for all parameters. For measurement of head size, fresh sperm samples were fixed in glutaraldehyde and slides were air-dried for 2 h. The samples were then stained with Diff-Quik� staining at 37�C. The area (Ar), perimeter (P), length (L), and width (W) of the heads of >100 spermatozoa per slide were measured (Sperm Class Analyzer�; Microptic S.L., Barcelona, Spain). Data were analyzed with the SAS ver8 system, and the Wilcoxon test was applied. The respective morphometric dimensions of the 2 groups were practically identical (Ar = 22; P = 18; L = 6; W = 4). The post-thaw recovery rates of spermatozoa from Group A were: TM: 60.1 � 29.3; PM: 54.8 � 36.0; viability: 99.4 � 8.0; acrosomes: 96.2 � 3.1; mitochondria: 70.9 � 15.5. The recovery rates for Group B were: TM: 78.7 � 13.8; PM: 69.0 � 18.8; viability: 93.8 � 5.2; acrosomes: 98.2 � 9.8; mitochondria: 72.5 � 22.5. Because of the high variability of recovery rates between males within each group, there were no statistical differences between the 2 groups. The absence of differences can be explained by the small number of males examined and the high variability between them. More studies are necessary to determine whether large sperm cells of brown bears are more susceptible to damage during cryopreservation. This work was supported in part by CANTUR S.A. and CICYT (CGL 2004-0278/BOS).


2018 ◽  
Vol 65 (6) ◽  
pp. 2049-2056 ◽  
Author(s):  
Juan F. García Marín ◽  
Luis J. Royo ◽  
Alvaro Oleaga ◽  
Elena Gayo ◽  
Olga Alarcia ◽  
...  

1997 ◽  
Vol 81 (1-2) ◽  
pp. 91-95 ◽  
Author(s):  
Jens Thomas Sagør ◽  
Jon E. Swenson ◽  
Eivin Røskaft
Keyword(s):  

2013 ◽  
Vol 304 (1) ◽  
pp. R43-R49 ◽  
Author(s):  
Inge G. Revsbech ◽  
Hans Malte ◽  
Ole Fröbert ◽  
Alina Evans ◽  
Stéphane Blanc ◽  
...  

During winter hibernation, brown bears ( Ursus arctos) reduce basal O2 consumption rate to ∼25% compared with the active state, while body temperature decreases moderately (to ∼30°C), suggesting a temperature-independent component in their metabolic depression. To establish whether changes in O2 consumption during hibernation correlate with changes in blood O2 affinity, we took blood samples from the same six individuals of hibernating and nonhibernating free-ranging brown bears during winter and summer, respectively. A single hemoglobin (Hb) component was detected in all samples, indicating no switch in Hb synthesis. O2 binding curves measured on red blood cell lysates at 30°C and 37°C showed a less temperature-sensitive O2 affinity than in other vertebrates. Furthermore, hemolysates from hibernating bears consistently showed lower cooperativity and higher O2 affinity than their summer counterparts, regardless of the temperature. We found that this increase in O2 affinity was associated with a significant decrease in the red cell Hb-cofactor 2,3-diphosphoglycerate (DPG) during hibernation to approximately half of the summer value. Experiments performed on purified Hb, to which DPG had been added to match summer and winter levels, confirmed that the low DPG content was the cause of the left shift in the Hb-O2 equilibrium curve during hibernation. Levels of plasma lactate indicated that glycolysis is not upregulated during hibernation and that metabolism is essentially aerobic. Calculations show that the increase in Hb-O2 affinity and decrease in cooperativity resulting from decreased red cell DPG may be crucial in maintaining a fairly constant tissue oxygen tension during hibernation in vivo.


2020 ◽  
Vol 56 (1) ◽  
pp. 251 ◽  
Author(s):  
Ana Balseiro ◽  
Luis José Royo ◽  
Elena Gayo ◽  
Juan Francisco García Marín

Author(s):  
Alessia Mariacher ◽  
Claudia Eleni ◽  
Rosario Fico ◽  
Stefania Perrucci
Keyword(s):  

Animals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 183
Author(s):  
Age Kärssin ◽  
Liidia Häkkinen ◽  
Annika Vilem ◽  
Pikka Jokelainen ◽  
Brian Lassen

In this study, we summarize Trichinella findings from four wild, free-ranging host species from Estonia during 2007–2014. Trichinella spp. larvae were detected in 281 (0.9%, 95% confidence interval (CI) 0.8–1.0) of 30,566 wild boars (Sus scrofa), 63 (14.7%, 95% CI 11.6–18.3) of 429 brown bears (Ursus arctos), 59 (65.56%, 95% CI 55.3–74.8) of 90 Eurasian lynxes (Lynx lynx), and three (60.0%, 95% CI 18.2–92.7) of five badgers (Meles meles). All four European Trichinella species were detected: T. britovi in 0.7% of the wild boars, 7.2% of the brown bears, 45.6% of the lynxes, and 40.0% of the badgers; T. nativa in 0.1% of the wild boars, 5.8% of the brown bears, and 20.0% of the lynxes; T. pseudospiralis in 0.02% the wild boars; and T. spiralis in 0.03% of the wild boars and 4.4% of the lynxes. The results include the first description from Estonia of T. britovi in brown bear and badgers, T. pseudospiralis in wild boars, and T. spiralis in wild boars and lynxes. The results indicate high infection pressure in the sylvatic cycles across the years—illustrating continuous risk of spillover to domestic cycles and of transmission to humans.


2020 ◽  
Vol 183 ◽  
pp. 109166 ◽  
Author(s):  
Maja Lazarus ◽  
Tatjana Orct ◽  
Agnieszka Sergiel ◽  
Lana Vranković ◽  
Vlatka Filipović Marijić ◽  
...  

2012 ◽  
Vol 90 (6) ◽  
pp. 753-757 ◽  
Author(s):  
Johanna Painer ◽  
Andreas Zedrosser ◽  
Jon M. Arnemo ◽  
Åsa Fahlman ◽  
Sven Brunberg ◽  
...  

We compared anesthetic protocols with different doses of tiletamine–zolazepam (TZ) combined with medetomidine (M) for 288 yearling brown bear ( Ursus arctos L., 1758) immobilizations with the objective of finding a combination of doses that would provide fast induction with a duration of anesthesia long enough to minimize the need for administering additional drug. The duration of induction time and immobilization was dose-dependent. Increasing the M dose resulted in significantly shorter induction times and a lower probability of giving supplemental drugs. Increasing the TZ dose prolonged duration of anesthesia. For yearling brown bears in Scandinavia, captured shortly after den emergence in April and May, we recommend total dart doses of 1.0–1.66 mg M/dart, plus 62.5–125 mg TZ/dart, depending on the individual requirements for the length and depth of anaesthesia.


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