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1.
J Zoo Wildl Med ; 32(3): 305-19, 2001 Sep.
Article in English | MEDLINE | ID: mdl-12785678

ABSTRACT

To evaluate the association between corneal lipid infiltration (corneal arcus) and dietary cholesterol in Cuban tree frogs (Osteopilus septentrionalis), 47 wild-caught frogs were fed diets of either regular or high-cholesterol crickets containing 0.7% and 1.7% cholesterol dry matter, respectively. Serum total cholesterol and triglycerides were measured when the frogs were euthanized after 17 mo. In a subsample of frogs, serum lipoproteins were characterized using high-performance liquid chromatography. The first case of corneal lipid deposition occurred in a female frog after 13 mo on the high-cholesterol diet. In the subsequent 4 mo, 5/11 males and 11/35 females developed the disease. Four of these affected frogs were females on the regular diet. Frogs with corneal lipid deposition had elevated serum total cholesterol (27.3 +/- 19.8 mmol/L) and low-density lipoproteins (LDL, 17.8 +/- 18.9 mmol/L) compared with unaffected captive frogs (16.5 +/- 20.4 and 9.0 +/- 7.6 mmol/L, respectively). Corneal lipid deposition was more prevalent in frogs on the high-cholesterol diet, and this group had higher serum total cholesterol (34.1 +/- 15.2 mmol/L in females, 22.8 +/- 14.8 mmol/L in males) than did frogs on the diet of regular crickets (12.3 +/- 8.7 mmol/L in females, 10.4 +/- 3.1 mmol/L in males). Captive frogs on both diets had higher serum total cholesterol than did wild frogs (3.1 +/- 2.1 mmo/L in females, 5.3 +/- 2.6 mmo/L in males). This additional serum cholesterol was primarily carried on very low-density lipoproteins (VLDL) and LDL rather than high-density lipoproteins (HDL), as indicated by the significantly higher ratio of VLDL cholesterol and LDL cholesterol over HDL cholesterol in captive frogs compared with wild frogs. Elevation in this ratio was significantly higher in captive females than in captive males. There was no evidence that increased serum cholesterol in captive females was directly related to the process of vitellogenesis.


Subject(s)
Anura/metabolism , Cholesterol, Dietary/administration & dosage , Corneal Diseases/veterinary , Lipidoses/veterinary , Lipids/blood , Animals , Animals, Wild , Animals, Zoo , Anura/blood , Cholesterol/blood , Cholesterol, Dietary/adverse effects , Corneal Diseases/blood , Corneal Diseases/etiology , Female , Lipid Metabolism , Lipidoses/blood , Lipidoses/etiology , Male , Random Allocation , Seasons , Triglycerides/blood , Vitellogenesis/physiology
2.
s.l; s.n; 1998. 23 p. ilus, tab, graf.
Non-conventional in English | Sec. Est. Saúde SP, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1235467

ABSTRACT

The cutaneous deposition disorders are a group of unrelated conditions characterized by the presence of either endogenous or exogenous substances within the dermis or the subcutis. Part I of this two-part series will focus on metabolic processes involved in the endogenous deposition in the various forms of amyloidosis, porphyria, colloid milium, and lipoid proteinosis. We will also review the clinical, histologic, biochemical, and ultrastructural findings relevant to each disorder. Basic mechanisms of pathogenesis, diagnostic modalities, and treatment options are also discussed.


Subject(s)
Humans , Amyloidosis/complications , Amyloidosis/diagnosis , Amyloidosis/etiology , Amyloidosis/metabolism , Amyloidosis/pathology , Amyloidosis/therapy , Skin Diseases, Metabolic/diagnosis , Skin Diseases, Metabolic/etiology , Skin Diseases, Metabolic/metabolism , Skin Diseases, Metabolic/pathology , Skin Diseases, Metabolic/therapy , Skin Diseases/diagnosis , Skin Diseases/etiology , Skin Diseases/metabolism , Skin Diseases/pathology , Skin Diseases/therapy , Lipidoses/diagnosis , Lipidoses/etiology , Lipidoses/metabolism , Lipidoses/pathology , Lipidoses/therapy , Skin/metabolism , Skin/pathology , Porphyrias/diagnosis , Porphyrias/etiology , Porphyrias/metabolism , Porphyrias/pathology , Porphyrias/therapy , Lipoid Proteinosis of Urbach and Wiethe/diagnosis , Lipoid Proteinosis of Urbach and Wiethe/etiology , Lipoid Proteinosis of Urbach and Wiethe/metabolism , Lipoid Proteinosis of Urbach and Wiethe/pathology , Lipoid Proteinosis of Urbach and Wiethe/therapy
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