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1.
J Comp Physiol B ; 190(6): 811-822, 2020 11.
Article in English | MEDLINE | ID: mdl-32815023

ABSTRACT

Immune responses to nitrogen gas bubbles, particularly activation of inflammation via the complement cascade, have been linked to the development of symptoms and damage associated with decompression sickness (DCS) in humans. Marine mammals were long thought not to be susceptible to such dive-related injury, yet evidence of DCS-like injury and new models of tissue nitrogen super-saturation suggest that bubbles may routinely form. As such, it is possible that marine mammals have protective adaptations that allow them to deal with a certain level of bubble formation during normal dives, without acute adverse effects. This work evaluated the complement response, indicative of inflammation, to in vitro nitrogen bubble exposures in several marine mammal species to assess whether a less-responsive immune system serves a protective role against DCS-like injury in these animals. Serum samples from beluga (Delphinapterus leucas), and harbor seals (Phoca vitulina) (relatively shallow divers) and deep diving narwhal (Monodon monoceros), and Weddell seals (Leptonychotes weddellii) were exposed to nitrogen bubbles in vitro. Complement activity was evaluated by measuring changes in the terminal protein C5a in serum, and results suggest marine mammal complement is less sensitive to gas bubbles than human complement, but the response varies between species. Species-specific differences may be related to dive ability, and suggest moderate or shallow divers may be more susceptible to DCS-like injury. This information is an important consideration in assessing the impact of changing dive behaviors in response to anthropogenic stressors, startle responses, or changing environmental conditions that affect prey depth distributions.


Subject(s)
Beluga Whale/blood , Complement C5a/analysis , Seals, Earless/blood , Whales/blood , Animals , Beluga Whale/immunology , Complement Activation/drug effects , Complement C5a/immunology , Nitrogen/pharmacology , Seals, Earless/immunology , Whales/immunology
2.
Article in English | MEDLINE | ID: mdl-32114311

ABSTRACT

Peptidylarginine deiminases (PADs) are a family of phylogenetically conserved calcium-dependent enzymes which cause post-translational protein deimination. This can result in neoepitope generation, affect gene regulation and allow for protein moonlighting via functional and structural changes in target proteins. Extracellular vesicles (EVs) carry cargo proteins and genetic material and are released from cells as part of cellular communication. EVs are found in most body fluids where they can be useful biomarkers for assessment of health status. Here, serum-derived EVs were profiled, and post-translationally deiminated proteins and EV-related microRNAs are described in 5 ceataceans: minke whale, fin whale, humpback whale, Cuvier's beaked whale and orca. EV-serum profiles were assessed by transmission electron microscopy and nanoparticle tracking analysis. EV profiles varied between the 5 species and were identified to contain deiminated proteins and selected key inflammatory and metabolic microRNAs. A range of proteins, critical for immune responses and metabolism were identified to be deiminated in cetacean sera, with some shared KEGG pathways of deiminated proteins relating to immunity and physiology, while some KEGG pathways were species-specific. This is the first study to characterise and profile EVs and to report deiminated proteins and putative effects of protein-protein interaction networks via such post-translationald deimination in cetaceans, revealing key immune and metabolic factors to undergo this post-translational modification. Deiminated proteins and EVs profiles may possibly be developed as new biomarkers for assessing health status of sea mammals.


Subject(s)
Cetacea/blood , Citrullination , Extracellular Vesicles/chemistry , Animals , Biomarkers/analysis , Biomarkers/blood , Blood Proteins/analysis , Blood Proteins/genetics , Cetacea/genetics , Extracellular Vesicles/genetics , MicroRNAs/blood , MicroRNAs/genetics , Phylogeny , Protein Interaction Maps , Protein-Arginine Deiminases/blood , Protein-Arginine Deiminases/genetics , Proteins/analysis , Proteins/genetics , Whales/blood , Whales/genetics
3.
Gen Comp Endocrinol ; 252: 103-110, 2017 10 01.
Article in English | MEDLINE | ID: mdl-28757434

ABSTRACT

Until now, physiological stress assessment of large whales has predominantly focused on adrenal glucocorticoid (GC) measures. Elevated GC concentrations in feces (fGC) are known to reflect stressful disturbances, such as fishing gear entanglement and human-generated underwater noise, in North Atlantic right whales (Eubalaena glacialis). However, there can be considerable variation in GC production as a function of sex and life history stage, which may confound the interpretation of fGC levels. Additionally, GC antibodies used in immunoassays can cross-react with other fecal metabolites (i.e., non-target steroids), potentially influencing fGC data. Here, aldosterone concentrations (fALD; aldosterone and related metabolites) were measured in fecal samples from right whales (total n=315 samples), including samples from identified individuals of known life history (n=82 individual whales), to evaluate its utility as a complementary biomarker to fGC for identifying adrenal activation. Concentrations of fALD were positively correlated with fGCs in right whales (r=0.59, P<0.001), suggesting concurrent secretion of these hormones by the adrenal gland. However, fALD levels were less influenced by concentrations of reproductive steroids in feces, minimizing the potential confounder of assay cross-reactivity in samples with highly skewed hormone ratios. Across different life history states for right whales, fALD concentrations showed similar patterns to those reported for fGC, with higher levels in pregnant females (35.9±7.6ng/g) followed by reproductively mature males (9.5±0.9ng/g) (P<0.05), providing further evidence of elevated adrenal activation in these groups of whales. The addition of fALD measurement as a biomarker of adrenal activation may help distinguish between intrinsic and external causes of stress hormone elevations in large whales, as well as other free-living wildlife species, providing a more comprehensive approach for associating adrenal activation with specific natural and anthropogenic stressors.


Subject(s)
Adrenal Glands/metabolism , Aldosterone/metabolism , Feces/chemistry , Glucocorticoids/metabolism , Whales/blood , Animals , Biomarkers/metabolism , Female , Male , Radioimmunoassay , Reproducibility of Results
4.
J Vet Med Sci ; 74(3): 293-300, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21997236

ABSTRACT

This study is the first report on circulating testosterone and inhibin levels in a species of whales, the beluga. Circulating testosterone and immunoreactive (ir-) inhibin levels in two captive male belugas ("Nack", originally from Canada and "Duke", from the Okhotsk Sea) were measured every month for 9 years between 1995 and 2003. Assuming that clearly increased testosterone levels in the circulation indicates that the belugas had reached sexual maturity, at the ages of 10 ("Nack") and 11 years old ("Duke"). Their testosterone levels before the significant increase (pre-pubertal) were 0.42 ± 0.07 ng/ml (n=18) and 0.35 ± 0.10 ng/ml (n=18) and, those of after the increase (maturity) were 1.65 ± 0.14 ng/m l (n=74) and 2.06 ± 0.14 ng/ml (n=74). Circulating ir-inhibin levels before sexual maturity were 0.78 ± 0.04 ng/ml (n=18) and 0.64 ± 0.04 ng/ml (n=15) and, after sexual maturity were 0.52 ± 0.02 ng/ml (n=56) and 0.43 ± 0.02 ng/ml (n=67). Seasonal changes were observed in the testosterone levels after sexual maturity and the levels increased during March and April in Canadian origin "Nack", and peaked in February in Okhotsk origin "Duke". Circulating ir-inhibin level gradually decreased as they aged. A negative correlation between the circulating testosterone and ir-inhibin was observed. No seasonal changes were observed in the ir-inhibin levels after sexual maturity. These data will surely correspond to clarification of endocrinology and the successful reproduction of the beluga.


Subject(s)
Aging , Inhibins/blood , Testosterone/blood , Whales/blood , Whales/physiology , Animals , Body Size , Male , Whales/growth & development
5.
Environ Sci Technol ; 44(10): 3732-8, 2010 May 15.
Article in English | MEDLINE | ID: mdl-20426459

ABSTRACT

In this study, we determined the residue levels and patterns of polychlorinated biphenyls (PCBs) and hydroxylated PCBs (OH-PCBs) in the blood from eight species of toothed whales and three species of baleen whales stranded along the Japanese coast during 1999-2007. Penta- through hepta-chlorinated PCB congeners were the dominant homologue groups in all cetaceans. In contrast, specific differences in the distribution of dominant OH-PCB isomers and homologues were found among the cetacean species. In five species of toothed whales (melon-headed whale, Stejneger's beaked whale, Pacific white-sided dolphin, Blainville's beaked whale, and killer whale), the predominant homologues were OH-penta-PCBs followed by OH-tetra-PCBs and OH-tri-PCBs. The predominant homologues of finless porpoise and beluga whale were OH-penta-PCBs followed by OH-hexa-PCBs and OH-tri-PCBs. The predominant OH-PCB isomers were para-OH-PCBs such as 4OH-CB26, 4'OH-CB25/4'OH-CB26/4OH-CB31, 4OH-CB70, 4'OH-CB72, 4'OH-CB97, 4'OH-CB101/4'OH-CB120, and 4OH-CB107/4'OH-CB108 in toothed whales. In three baleen whales (common minke whale, Bryde's whale, and humpback whale) and in sperm whale (which is a toothed whale), OH-octa-PCB (4OH-CB202) was the predominant homologue group accounting for 40-80% of the total OH-PCB concentrations. The differences in concentrations and profiles of OH-PCBs may suggest species-specific diets, metabolic capability, and the transthyretin (TTR) binding specificity. These results reveal that the accumulation profiles of OH-PCBs in cetacean blood are entirely different from the profiles found in pinnipeds, polar bear, and humans.


Subject(s)
Polychlorinated Biphenyls/blood , Water Pollutants, Chemical/blood , Whales/blood , Animals , Female , Gas Chromatography-Mass Spectrometry , Hydroxylation , Male , Quality Control , Species Specificity
6.
Zygote ; 12(2): 125-32, 2004 May.
Article in English | MEDLINE | ID: mdl-15460107

ABSTRACT

The present study aimed to determine the relationship among changes in the number of preantral follicles and concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), progesterone (P4), androstenedione (A) and estradiol-17beta (E2) in the fetal heart, umbilical cord and maternal blood. Primordial follicles had already appeared in a 20 cm fetus and primary follicles were observed in a 50 cm fetus. In a 70 cm fetus, the number of primordial and primary follicles increased rapidly and secondary follicles were present. The concentrations of LH and FSH did not change between 20 cm and 160 cm in fetal length. When the fetal length became > 70 cm, serum levels in the fetus, umbilical cord and mothers, and E2 levels in umbilical cord increased synchronously (p < 0.05). These results showed increases in the number of preantral follicles in the Antarctic minke whale fetal ovary along with fetal growth during the early gestation period. These findings suggest that the change in preantral follicles was associated with changes in the concentration of steroids in early gestation periods. The changes in steroid concentrations in the fetal and umbilical cord blood and the increased number of preantral follicles were coincident at around 70 cm in fetal length, whereas the growth and differentiation of primordial and primary follicles appeared to be independent of FSH and LH.


Subject(s)
Hormones/blood , Ovarian Follicle/embryology , Whales/blood , Whales/embryology , Androstenedione/blood , Androstenedione/metabolism , Animals , Antarctic Regions , Estradiol/blood , Estradiol/metabolism , Female , Fetal Blood/metabolism , Fetal Heart/metabolism , Follicle Stimulating Hormone/blood , Follicle Stimulating Hormone/metabolism , Gestational Age , Hormones/metabolism , Luteinizing Hormone/blood , Luteinizing Hormone/metabolism , Pregnancy , Progesterone/blood , Progesterone/metabolism , Whales/metabolism
7.
Inorg Chem ; 42(5): 1456-61, 2003 Mar 10.
Article in English | MEDLINE | ID: mdl-12611510

ABSTRACT

The iron complex of hemiporphycene, a molecular hybrid of porphyrin with porphycene, was incorporated into the apomyoglobin pocket to examine ligand binding ability of the iron atom in the novel porphyrinoid. Apomyoglobin was successfully coupled with a stoichiometric amount of ferric hemiporphycene to afford the reconstituted myoglobin equipped with the iron coordination structure of native protein. Cyanide, imidazole, and fluoride coordinated to the ferric protein with affinities comparable with those for native myoglobin. The ferrous myoglobin was functionally active to bind O(2) and CO reversibly at pH 7.4 and 20 degrees C. The O(2) affinity is 12-fold higher than that of native myoglobin while the CO affinity is slightly lower, suggesting decreased discrimination between O(2) and CO in the heme pocket. The functional anomaly was interpreted to reflect increased sigma-bonding character in the Fe(II)-O(2) bond. In contrast with 6-coordinate native NO protein, the NO myoglobin containing ferrous hemiporphycene is in a mixed 5- and 6-coordinate state. This observation suggests that the in-plane configuration of the iron atom in hemiporphycene is destabilized by NO. Influence of the core deformation was also detected with both the infrared absorption for the ferrous CO derivative and electron paramagnetic resonance for ferric imidazole complex. Anomalies in the ferric and ferrous derivatives were ascribed to the modified iron-N(pyrrole) interactions in the asymmetric metallo core of hemiporphycene.


Subject(s)
Iron/chemistry , Metalloporphyrins/chemistry , Metalloporphyrins/metabolism , Myoglobin/chemistry , Myoglobin/metabolism , Porphyrins/chemistry , Animals , Apoproteins/chemistry , Apoproteins/metabolism , Electron Spin Resonance Spectroscopy , Hydrogen-Ion Concentration , Iron/metabolism , Ligands , Models, Molecular , Molecular Structure , Porphyrins/metabolism , Whales/blood
9.
Theriogenology ; 55(5): 1127-41, 2001 Mar 15.
Article in English | MEDLINE | ID: mdl-11322240

ABSTRACT

This study investigated plasma and pituitary concentrations of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) and steroid hormones (progesterone: P4, testosterone:T, estradiol-17beta: E2) by enzyme-immunoassay (EIA) in minke whales (Balaenoptera acutorostrata) captured during the feeding season (December to March) in the Antarctic Ocean. Plasma FSH and LH levels in female minke whales were higher (P <0.05) than in male whales. Although the pituitary weight was not significantly different between male and female whales, pituitary FSH and LH levels were higher in females than in males (P<0.01) and mature whales than immature whales (P<0.05). Plasma levels of FSH, T and E2 were not significantly different between immature and mature male whales, but plasma LH and pituitary FSH and LH levels were higher (P<0.05) in mature than in immature whales. In both immature and mature whales regardless of gender, pituitary FSH and LH levels were correlated significantly (r=0.69: P<0.01). In mature male whales, plasma T and E2 levels (r=0.60: P<0.01), and testis weight and plasma T levels (r=0.46: P <0.05) were correlated. In immature female whales, plasma FSH and LH levels were highly correlated (r=0.68: P<0.001), but were not for mature female whales. The results show that gender and maturity influence gonadal and pituitary function of minke whales during the feeding season.


Subject(s)
Follicle Stimulating Hormone/metabolism , Luteinizing Hormone/metabolism , Pituitary Gland/metabolism , Whales/metabolism , Age Factors , Animals , Antarctic Regions , Estradiol/blood , Estradiol/metabolism , Feeding Behavior/physiology , Female , Follicle Stimulating Hormone/blood , Immunoenzyme Techniques , Linear Models , Luteinizing Hormone/blood , Male , Pituitary Gland/chemistry , Pregnancy , Progesterone/blood , Progesterone/metabolism , Reproduction/physiology , Seasons , Sex Factors , Testosterone/blood , Testosterone/metabolism , Whales/blood , Whales/physiology
10.
J Wildl Dis ; 37(2): 332-41, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11310885

ABSTRACT

Serum samples were collected from 42 harpooned minke whales (Balaenoptera acutorostrata) during commercial whaling off the coast of northern Norway (1997 and 1998) and analyzed for serum chemistry parameters in order to find clinical reference values for the northeastern Atlantic stock of this species. Mean and median values, as well as standard deviation and 90% central range, are presented for 28 different serum chemistry parameters. Lipemia is a common finding in marine mammals such as the minke whale, and chemical analysis of lipemic serum samples may produce artifacts. We found statistically significant elevated values of total protein, globulin, aspartate aminotransferase (AST), alanine aminotransferase (ALT), sodium and chloride in strongly-lipemic compared to non-lipemic samples, all which may be artifacts due to interference of lipids with the methods used for analysis. In addition, we found significantly elevated levels of creatin kinase, lactate dehydrogenase (LDH), urea, uric acid and triglycerides, as well as a decrease in creatinine in the strongly lipemic samples. Reanalyzing serum samples after twelve mo storage at -20 C (n = 13) revealed reduction in the serum concentration of the enzymes ALT (42%), alkaline phosphatase (ALP; 10%), LDH (19%), gamma glutamyl transferase (17%) and amylase (11%), as well as for triglycerides (9%) and non-esterified fatty acids (16%). It is crucial that serum chemistry analysis is performed without delay after sampling. Possible changes in the values of some parameters due to the presence of high amounts of lipids or long term storage of samples must be considered when interpreting results from serum chemistry analysis in these animals.


Subject(s)
Blood Chemical Analysis/veterinary , Whales/blood , Alanine Transaminase/blood , Animals , Aspartate Aminotransferases/blood , Atlantic Ocean , Chlorides/blood , Creatine Kinase/blood , Female , L-Lactate Dehydrogenase/blood , Lipids/blood , Male , Sodium/blood , Triglycerides/blood , Uric Acid/blood
11.
Biochem Genet ; 38(7-8): 241-52, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11131338

ABSTRACT

Carbonic anhydrase (CA) expression was examined in the red cells of two mammals that have adapted to low oxygen stress: the llama, which has adapted to high altitudes, and the beluga (or white) whale, which routinely dives for extended periods. Immunodiffusion analyses of their Hb-free hemolysates and partial amino acid sequencing of their HPLC-separated nonheme proteins indicate that the low-activity CA I isozyme is the major nonheme protein in erythrocytes of both the beluga whale and the llama. The high-activity CA II isozyme was not detected in the whale red cells but was present at low levels in erythrocytes of the llama. These results suggest that the absence or decrease in the expression of the high-activity CA II isozyme may be advantageous under hypoxic conditions.


Subject(s)
Camelids, New World/blood , Carbonic Anhydrases/blood , Erythrocytes/enzymology , Whales/blood , Amino Acid Sequence , Animals , Camelus , Chromatography, High Pressure Liquid , Electrophoresis, Polyacrylamide Gel , Female , Humans , Male , Molecular Sequence Data , Oxygen , Sequence Alignment
12.
Dis Aquat Organ ; 42(2): 111-7, 2000 Aug 31.
Article in English | MEDLINE | ID: mdl-11023250

ABSTRACT

An eastern Pacific gray whale (Eschrichtius robustus) stranded off Pelican Point, Tomales Bay, California, USA, was examined for physiological parameters, prey, parasites and associated pathology. The whale was emaciated, and hematological examination revealed an elevation in hematocrit, serum sodium, potassium, electrolyte values and hypoglycemia. Parasites recovered included 5 species, 1 ectoparasite (Cyamus scammoni), and 4 helminths (Anisakis simplex, Ogmogaster antarcticus, Ogmogaster pentalineatus, Bolbosoma balanae) with the latter causing multifocal transmural abscesses. Histological examination indicated severe acute lung congestion, minimal, multifocal, lymphocytic, interstitial myocarditis, and mild hepatocellular and Kupffer cell hemosiderosis. The prey taxa present in the stomach indicated the whale was feeding on hard bottom communities prior to death.


Subject(s)
Helminthiasis, Animal/pathology , Whales/parasitology , Animals , California , Electrolytes/blood , Fatal Outcome , Gastrointestinal Contents/parasitology , Helminthiasis, Animal/complications , Hematocrit/veterinary , Host-Parasite Interactions , Hypoglycemia/veterinary , Lung/pathology , Male , Potassium/blood , Sodium/blood , Whales/blood
13.
Thromb Res ; 97(6): 481-90, 2000 Mar 15.
Article in English | MEDLINE | ID: mdl-10704658

ABSTRACT

The expression of high-molecular-weight and low-molecular-weight kininogen mRNAs in the whale liver was examined by reverse transcription-polymerase chain reaction. The nucleotide sequences of the high-molecular-weight and low-molecular-weight kininogen cDNAs were analyzed and deduced to the amino acid sequences. The high-molecular-weight kininogen composed of 609 amino acid residues with 18 signal peptides possessed the consensus sequences of the cysteine protease inhibitor domains I and II, the bradykinin domain, the histidine-rich region, and the prekallikrein-binding region. Except for the histidine-rich region, the overall homologies with bovine, human, and rat high-molecular-weight kininogens were 81%, 76%, and 62%, respectively. The low-molecular-weight kininogen is composed of 408 amino acid residues. The nucleotide sequence down to C(1200) as well as the amino acid sequence till Ile(382) is identical to that of the high-molecular-weight kininogen. The remaining low-molecular-weight kininogen-specific carboxy-terminal portion possessed an amino acid sequence similar to that of the land mammals. The overall homologies with bovine, human, and rat low-molecular-weight kininogens were 82%, 79%, and 64%, respectively. The amino acid sequences of both whale high-molecular-weight and low-molecular-weight kininogens are most similar to those of the bovine among the land mammals analyzed so far. An incubation of dolphin/whale plasma with human plasma kallikrein, or with bovine trypsin, in the presence of carboxypeptidase inhibitors generated bradykinin antigen as well as the spasmogenic activity to the estrous rat uterus. The amount of bradykinin released by the latter enzyme was almost double of the former, indicating that the dolphin/whale plasma contained similar concentrations of low-molecular-weight and high-molecular-weight kininogens.


Subject(s)
Kininogen, High-Molecular-Weight/genetics , Kininogen, Low-Molecular-Weight/genetics , Whales/genetics , Amino Acid Sequence , Animals , Base Sequence , Bradykinin/metabolism , Cattle , DNA, Complementary/chemistry , DNA, Complementary/genetics , Dolphins/blood , Factor XI/metabolism , Humans , Kallikreins/metabolism , Kininogen, High-Molecular-Weight/blood , Kininogen, Low-Molecular-Weight/blood , Molecular Sequence Data , Prekallikrein/metabolism , Protein Structure, Tertiary , Rats , Sequence Alignment , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Trypsin/metabolism , Whales/blood
14.
J Comp Pathol ; 122(1): 73-6, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10627393

ABSTRACT

Toxoplasmosis was diagnosed in two free-ranging beluga whales from the St Lawrence estuary, Quebec, Canada, in 1988 and 1998. Histologically, tachyzoites and bradyzoites were present in the brain, spleen, lymph nodes, adrenals and lungs of both animals, and in the thymus of one. These organisms were readily labelled by an indirect immunohistochemical method for Toxoplasma gondii antigens. In the lymph nodes, spleen and lungs the organisms were associated with histiocytic infiltration. In the brain of one animal they were associated with mild multifocal gliosis and haemorrhages. There was no evidence of concomitant morbillivirus infection. Serum samples were collected from 22 beluga whales stranded between 1995 and 1998 on the shores of the St Lawrence Estuary and examined for antibodies to T. gondii by the modified agglutination test. Antibody titres of s25 were found in six (27%) of the animals. This is the first confirmed report of toxoplasmosis in beluga whales.


Subject(s)
Toxoplasma/isolation & purification , Toxoplasmosis, Animal/pathology , Whales/parasitology , Animals , Antibodies, Protozoan/analysis , Antigens, Protozoan/immunology , Brain/parasitology , Fluorescent Antibody Technique, Indirect/veterinary , Male , Spleen/parasitology , Toxoplasma/immunology , Toxoplasmosis, Animal/blood , Whales/blood
15.
Aust Vet J ; 75(7): 512-4, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9258426

ABSTRACT

OBJECTIVE: To examine haematological features in five species of healthy, captive marine mammals. ANIMALS: Twenty bottlenose dolphins (Tursips truncatus), seven Pacific white-sided dolphins (Lagenorhynchus obliquidens), five Risso dolphins (Grampus griseus) and five false killer whales (Pseudorca crassidens). RESULTS AND CONCLUSION: The red blood cell count was 4.21 x 10(12)/L in bottlenose dolphins, 5.32 x 10(12)/L in Pacific white-sided dolphins, 4.35 x 10(12)/L in Risso dolphins and 4.43 x 10(12)/L in false killer whales. The haemoglobin concentration was 1.51 g/L and packed cell volume 44.7% in bottlenose dolphins; the corresponding values were 1.71 g/L and 48.9% in Pacific white-sided dolphins, 1.72 g/L and 49.4% in Risso dolphins, and 1.52 g/L and 47.8% in false killer whales. The white blood cell count was 7.097 x 10(9)/L in bottlenose dolphins, 5.928 x 10(9)/L in Pacific white-sided dolphins, 5.001 x 10(9)/L in Risso dolphins and 7.921 x 10(9)/L in false killer whales. There were no significant differences in these values among bottlenose dolphins and Pacific white-sided dolphins. The proportion of eosinophils in the differential leukocyte count ranged from 10.3% to 11.5% in bottlenose dolphins, Pacific white-sided dolphins and false killer whales, but was only 0.4% in Risso dolphins. The eosinophilic granules were larger in Risso dolphins and false killer whales than in bottlenose and Pacific white-sided dolphins.


Subject(s)
Dolphins/blood , Whales/blood , Animals , Basophils/cytology , Eosinophils/cytology , Erythrocyte Count/veterinary , Erythrocytes/cytology , Female , Hematologic Tests/methods , Hematologic Tests/veterinary , Hemoglobins/analysis , Leukocyte Count/veterinary , Leukocytes/cytology , Monocytes/cytology , Reference Values
16.
J Wildl Dis ; 32(1): 75-9, 1996 Jan.
Article in English | MEDLINE | ID: mdl-8627940

ABSTRACT

Sera of 19 male and female bowhead whales (Balaena mysticetus) collected near Barrow, Alaska (USA) between 30 August and 13 October 1992 were evaluated for 18 serum chemistry values. Male bowhead whales had significantly greater creatinine and sodium concentrations, and significantly lower glucose concentrations than females. Pregnant females had greater triglyceride levels than non-pregnant females. The mean concentrations of creatinine, blood urea nitrogen, alkaline phosphatase, total bilirubin, total protein, sodium, potassium, chloride, phosphorus, and calcium were similar to those previously reported from bowhead whales. High aspartate aminotransferase and creatinine kinase levels were attributed to muscle damage associated with harpooning.


Subject(s)
Pregnancy, Animal/blood , Sex Characteristics , Whales/blood , Animals , Blood Chemical Analysis/veterinary , Blood Glucose/analysis , Blood Proteins/analysis , Creatinine/blood , Female , Male , Pregnancy , Reference Values , Sodium/blood , Triglycerides/blood
17.
J Reprod Fertil ; 102(1): 237-44, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7799319

ABSTRACT

Blood samples and testes were collected from long-finned pilot whales (Globicephala melas) off the Faroe Islands at irregular intervals over a period of 3 years (July 1986-December 1989). Changes in testis mass (n = 674) and plasma testosterone concentrations (n = 214), measured by radioimmunoassay, were examined with respect to age, bodylength and bodymass of the animals. Corresponding to a rapid testicular growth (from 0.25 kg up to 1.9 kg), puberty occurred in male pilot whales of 4.6-5.7 m in bodylength, 1.2-1.9 tonnes in bodymass and 11-22 years of age. Changes in plasma testosterone concentrations confirmed this result, with very low values (< 2 ng ml-1) in immature animals (testis mass < 0.2 kg), followed by a sharp increase (from 2 to 29 ng ml-1) during the pubertal period, and the maintenance of high concentrations with large variability (> 1.5 ng ml-1 to 14 ng ml-1) in mature males. Testosterone concentrations were significantly correlated with testis mass (P < 0.001), but not with bodylength or age, and very large individual variations were observed in mature males. The average age, length and mass at the attainment of sexual maturity were estimated at 16.99 +/- 0.30 years, 5.162 +/- 0.013 m and 1.403 +/- 0.005 tonnes, respectively.


Subject(s)
Sexual Maturation/physiology , Testis/growth & development , Testosterone/blood , Whales/growth & development , Animals , Body Constitution/physiology , Body Weight/physiology , Male , Testis/anatomy & histology , Whales/blood
18.
J Biomol NMR ; 4(4): 491-504, 1994 Jul.
Article in English | MEDLINE | ID: mdl-8075538

ABSTRACT

Sequence-specific backbone 1H and 15N resonance assignments have been made for 95% of the amino acids in sperm whale myoglobin, complexed with carbon monoxide (MbCO). Many assignments for side-chain resonances have also been obtained. Assignments were made by analysis of an extensive series of homonuclear 2D spectra, measured with unlabeled protein, and both 2D and 3D 1H-15N-correlated spectra obtained from uniformly 15N-labeled myoglobin. Patterns of medium-range NOE connectivities indicate the presence of eight helices in positions that are very similar to those found in the crystal structures of sperm whale myoglobin. The resonance assignments of MbCO form the basis for determination of the solution structure and for hydrogen-exchange measurements to probe the stability and folding pathways of myoglobin. They will also form a basis for assignment of the spectra of single-site mutants with altered ligand-binding properties.


Subject(s)
Magnetic Resonance Spectroscopy , Myoglobin/chemistry , Amino Acid Sequence , Animals , Carbon Monoxide/chemistry , Hydrogen , Molecular Sequence Data , Nitrogen Isotopes , Protein Structure, Secondary , Recombinant Fusion Proteins/chemistry , Whales/blood
19.
J Endocrinol ; 134(3): 405-13, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1402548

ABSTRACT

Blood serum concentrations of testosterone and progesterone were measured in postmortem samples taken at sea from 814 fin whales (Balaenoptera physalus) caught during the summers (June-September) of 1981-1989. The ages of 781 of these animals were also assessed. The testosterone concentrations in samples from 352 males averaged 2 nmol/l; 41 samples had concentrations of 0.1 nmol/l or lower and 34 of these came from whales aged between 2 and 14 years and showed a Gaussian type of age distribution with a peak number at 7 to 8 years. The mean testosterone concentrations in the males increased by more than fourfold between June and August. Serum progesterone concentrations of the 462 females fell into three separate groups: (1) group I with values < or = 0.1 nmol/l; (2) group II with intermediate values of > 0.1 nmol/l but < 10 nmol/l; (3) group III with values of > or = 10 nmol/l. These three groups of females seemed to consist respectively of young sexually immature females, mature non-pregnant females and pregnant females. The age distribution in the groups indicated that puberty in females is attained chiefly between the ages of 7 and 10. The yearly pregnancy rate (that percentage of all females caught and studied in a year which had progesterone values > or = 10 nmol/l) was between 35% and 55%, except in 1987 when it was 67%. The yearly pregnancy rate would range from 56% to 93% if only mature females (i.e. those with serum progesterone > 0.1 nmol/l) were considered.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Gonadal Steroid Hormones/blood , Pregnancy, Animal/blood , Whales/blood , Animals , Estradiol/blood , Female , Male , Pregnancy , Progesterone/blood , Radioimmunoassay , Sexual Maturation/physiology , Testosterone/blood
20.
Biochem J ; 281 ( Pt 3): 725-8, 1992 Feb 01.
Article in English | MEDLINE | ID: mdl-1311173

ABSTRACT

An extensive set of data relating to the binding of oxygen by haemocyanin from the squid Todarodes sagittatus has been collected under various experimental conditions. The results obtained show that, within the range of physiological pH, the concentration of protons affects mainly the high-affinity state of the molecule without significantly affecting the low-affinity state. As far as the effect of temperature is concerned, the data show a characteristic feature which is very similar to that previously described in the case of haemoglobins from Arctic mammals such as reindeer (Rangifer tarandus) and musk ox. (Ovibos moschatus). The shape of the oxygen equilibrium curve shows strong temperature-dependence, since the overall heat of the binding of oxygen to the low-affinity state of the molecule is strongly exothermic and that to the high-affinity state is very close to zero. The results provide an outline of the intramolecular compromise that, through the interplay of temperature and protons, optimizes the loading and unloading of oxygen under the various environmental conditions experienced by this species of squid.


Subject(s)
Decapodiformes/metabolism , Hemocyanins/metabolism , Oxygen/blood , Protons , Animals , Hydrogen-Ion Concentration , Mammals/blood , Reindeer/blood , Temperature , Thermodynamics , Whales/blood
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