Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
1.
Vet Pathol ; 53(2): 425-35, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26823448

ABSTRACT

Chimpanzees (Pan troglodytes) have served as an important model for studies of reproductive diseases and aging-related disorders in humans. However, limited information is available about spontaneously occurring reproductive tract lesions in aging chimpanzees. In this article, the authors present histopathologic descriptions of lesions identified in the reproductive tract, including the mammary gland, of 33 female and 34 male aged chimpanzees from 3 captive populations. The most common findings in female chimpanzees were ovarian atrophy, uterine leiomyoma, adenomyosis, and endometrial atrophy. The most common findings in male chimpanzees were seminiferous tubule degeneration and lymphocytic infiltrates in the prostate gland. Other less common lesions included an ovarian granulosa cell tumor, cystic endometrial hyperplasia, an endometrial polyp, uterine artery hypertrophy and mineralization, atrophic vaginitis, mammary gland inflammation, prostatic epithelial hyperplasia, dilated seminal vesicles, a sperm granuloma, and lymphocytic infiltrates in the epididymis. The findings in this study closely mimic changes described in the reproductive tract of aged humans, with the exception of a lack of malignant changes observed in the mammary gland and prostate gland.


Subject(s)
Aging/pathology , Ape Diseases/pathology , Genital Diseases, Female/veterinary , Genital Diseases, Male/veterinary , Pan troglodytes , Animals , Disease Models, Animal , Female , Genital Diseases, Female/pathology , Genital Diseases, Male/pathology , Genitalia/pathology , Humans , Male , Retrospective Studies
2.
Vet Pathol ; 53(2): 417-24, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26792841

ABSTRACT

Cardiorenal syndrome involves disease and dysfunction of the heart that leads to progressive renal dysfunction. This study investigated the relationship between cardiac and renal disease in 91 aged chimpanzees at the Alamogordo Primate Facility by evaluation of the medical histories, metabolic parameters, functional measurements of the cardiovascular system, clinical pathology, and histopathology focused on the heart and kidney. Cardiac fibrosis was the most frequent microscopic finding in 82 of 91 animals (90%), followed by glomerulosclerosis with tubulointerstitial fibrosis in 63 of 91 (69%). Cardiac fibrosis with attendant glomerulosclerosis and tubulointerstitial fibrosis was observed in 58 of 91 animals (63%); there was a statistically significant association between the 2 conditions. As the severity of cardiac fibrosis increased, there was corresponding increase in severity of glomerulosclerosis with tubulointerstitial fibrosis. Altered metabolic, cardiovascular, and clinical pathology parameters indicative of heart and kidney failure were commonly associated with the moderate to severe microscopic changes, and concurrent heart and kidney failure were considered the cause of death. The constellation of findings in the chimpanzees were similar to cardiorenal syndrome in humans.


Subject(s)
Ape Diseases/pathology , Cardio-Renal Syndrome/veterinary , Kidney/pathology , Myocardium/pathology , Pan troglodytes , Animals , Cardio-Renal Syndrome/pathology , Female , Fibrosis/pathology , Fibrosis/veterinary , Humans , Male , Retrospective Studies
3.
J Biomark ; 2013: 709740, 2013.
Article in English | MEDLINE | ID: mdl-26317021

ABSTRACT

C-reactive protein, a conserved acute-phase protein synthesized in the liver and involved in inflammation, infection, and tissue damage, is an informative biomarker for human cardiovascular disease. Out of 258 captive adult common chimpanzees (Pan troglodytes) assayed for CRP, 27.9% of the data were below the quantitation limit. Data were analyzed by the Kaplan-Meier method and results compared to other methods for handling censored data (including deletion, replacement, and imputation). Kaplan-Meier results demonstrated a modest age effect and a strong effect of HCV infection in reducing CRP but did not allow inference of reference intervals. Results of other methods varied considerably. Substitution schemes differed widely in statistical significance, with estimated group means biased by the size of the substitution constant, while inference of unbiased reference intervals was impossible. Single imputation gave reasonable statistical inferences but unreliable reference intervals. Multiple imputation gave reliable results, for both statistical inference and reference intervals, and was comparable to the Kaplan-Meier standard. Other methods should be avoided. CRP did not predict cardiovascular disease, but CRP levels were reduced by 50% in animals with hepatitis C infection and showed inverse relationships with 2 liver function enzymes. Results suggested that hsCRP can be an informative biomarker of chronic hepatic dysfunction.

4.
Am J Primatol ; 73(7): 665-70, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21442632

ABSTRACT

Uterine leiomyomata are common, affecting 70-80% of women between 30 and 50 years of age. Leiomyomata have been reported for a variety of primate species, although prevalence rates and treatments have not been widely reported. The prevalence, diagnosis, and treatment of uterine leiomyomata in the Alamogordo Primate Facility and the Keeling Center for Comparative Medicine and Research were examined. Uterine leiomyomata were diagnosed in 28.4% of chimpanzees with an average age at diagnosis of 30.4 ± 8.0 years. Advanced age (>30 years) was related to an increase in leiomyomata and use of hormonal contraception was related to a decrease in leiomyomata. As the captive chimpanzee population ages, the incidence of leiomyomata among female chimpanzees will likely increase. The introduction of progesterone-based contraception for nonbreeding research and zoological chimpanzees may reduce the development of leiomyomata. Finally, all chimpanzee facilities should institute aggressive screening programs and carefully consider treatment plans.


Subject(s)
Leiomyoma/veterinary , Pan troglodytes , Primate Diseases/diagnosis , Primate Diseases/epidemiology , Uterine Neoplasms/veterinary , Age Factors , Animals , Contraception/veterinary , Female , Leiomyoma/diagnosis , Leiomyoma/epidemiology , Leiomyoma/therapy , New Mexico/epidemiology , Prevalence , Primate Diseases/therapy , Progesterone/therapeutic use , Texas/epidemiology , Uterine Neoplasms/diagnosis , Uterine Neoplasms/epidemiology , Uterine Neoplasms/therapy
5.
J Med Primatol ; 40(3): 171-80, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21323674

ABSTRACT

BACKGROUND: Cardiovascular disease is the primary cause of morbidity and mortality among captive chimpanzees. But there are no clinical definitions of normotension or hypertension in chimpanzees. METHODS: We analyzed 1 year of blood pressure (BP) data from a population of 261 healthy captive adult chimpanzees using a consistent set of criteria to ascertain health. RESULTS: Systolic BP varied by body weight. Diastolic BP varied by age. Median normotension was 126/63 mmHg, with an upper limit of 147/84 mmHg. We defined categories of pre-hypertension (148/85-153/88 mmHg) and hypertension (≥154/89 mmHg). The prevalence of elevated BP was 15%. The relative risk of mortality was 2.60, compared to normotensive animals. CONCLUSIONS: We used contemporary methods from human laboratory medicine to define reliable reference intervals for chimpanzee BP. Results allow accurate diagnosis of hypertension and pre-hypertension, and demonstrate an effect of elevated BP on mortality.


Subject(s)
Blood Pressure , Hypertension/diagnosis , Hypertension/epidemiology , Pan troglodytes/blood , Age Factors , Animals , Body Weight , Cardiovascular Diseases/diagnosis , Cardiovascular Diseases/epidemiology , Female , Health Status , Male , New Mexico/epidemiology , Prehypertension/diagnosis , Prehypertension/epidemiology , Prevalence , Reference Values , Risk Factors
6.
Microb Pathog ; 9(3): 199-211, 1990 Sep.
Article in English | MEDLINE | ID: mdl-1708078

ABSTRACT

Oral streptococci vary in their susceptibility to salivary agglutinin-mediated aggregation. To understand the molecular basis of this specificity, the structure and function of receptors for agglutinin from Streptococcus mutans KPSK2 (MSL-1) and Streptococcus sanguis M5 (SSP-5) were compared. Immunological screening of an S. mutans KPSK2 genomic DNA library yielded two identical clones expressing a streptococcal protein that co-migrated with a 220 kDa peptide in SDS extracts from this organism. This protein inhibited agglutinin-mediated aggregation of S. mutans KPSK2 in a dose-dependent manner. The MSL-1 gene is homologous to the S. mutans SpaP and pac genes although single base substitutions alter several amino acids. MSL-1 is also similar to the agglutinin receptor (SSP-5) cloned from S. sanguis M5. All three proteins, MSL-1, P1, and SSP-5 share at least one epitope since monoclonal and polyclonal anti-SSP-5 antibodies react with both MSL-1 and P1. However, other monoclonal antibodies are specific for SSP-5 and appear to react with a peptide domain exhibiting little homology to MSL-1 or P1. Sugar inhibition studies showed that agglutinin-mediated aggregation of S. mutans KPSK2 was most potently inhibited by fucose and lactose. Sialic acid, a potent inhibitor of S. sanguis aggregation, had no effect on the interaction of agglutinin with S. mutans KPSK2. These results suggest that while the MSL-1 and SSP-5 proteins are genetically and immunologically related, their specificity for binding sites on agglutinin differs.


Subject(s)
Adhesins, Bacterial , Agglutinins/metabolism , Receptors, Mitogen/genetics , Saliva/metabolism , Streptococcus mutans/genetics , Streptococcus sanguis/genetics , Amino Acid Sequence , Antibodies, Monoclonal , Blotting, Western , Cloning, Molecular , Epitopes , Genes, Bacterial , Humans , Molecular Sequence Data , Receptors, Mitogen/metabolism , Restriction Mapping , Sequence Homology, Nucleic Acid , Streptococcus mutans/metabolism , Streptococcus sanguis/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...