Diabetes insipidus central em felino jovem / Central diabetes insipidus in a young feline

Background: Central diabetes insipidus (CDI) is an endocrine disorder caused by the failure to produce, transport, orrelease ADH. This disease may show a primary etiology (idiopathic or congenital) or a secondary one (trauma or neoplasms). It is characterized by signs such as polyuria and polydipsia. The definitive diagnosis is obtained by the two-stepwater deprivation test; the absence of adequate urinary concentration in the first stage confirms the diagnosis of diabetesinsipidus and, in the second stage, the response to the application of synthetic desmopressin confirms a central origin.Because CDI is rare in felines, the aim of this study was to report the occurrence of a case of CDI, probably of congenitalprimary origin, in an 8-month-old kitten.Case: An 8-month-old male feline, castrated, 3.2 kg, was brought to consultation with a report of polydipsia, polyuria,smaller size and weight, and lower activity when compared to his brother, for several months. On physical examination,lethargy, body score 2/5, and mild dehydration were noted, as well as deciduous teeth that should have already been replaced. Abdominal ultrasound and laboratory tests were requested, which ruled out chronic kidney disease (CKD), diabetesmellitus (DM), hyperadrenocorticism (HAC), and hyperthyroidism. Due to the fact that urinalysis evidenced hyposthenuria(urinary density [UD] 1.004), CDI was suspected. The patient underwent a water deprivation test and, after 7.5 h, lost4.7% of his initial weight, while UD was 1.012, confirming the diagnosis of DI. The investigation then proceeded to theevaluation of the response to synthetic desmopressin by the application of 5 U IM. Two h later, UD was 1.019, confirming...

Diabetes insipidus central em felino jovem / Central diabetes insipidus in a young feline

Background: Central diabetes insipidus (CDI) is an endocrine disorder caused by the failure to produce, transport, orrelease ADH. This disease may show a primary etiology (idiopathic or congenital) or a secondary one (trauma or neoplasms). It is characterized by signs such as polyuria and polydipsia. The definitive diagnosis is obtained by the two-stepwater deprivation test; the absence of adequate urinary concentration in the first stage confirms the diagnosis of diabetesinsipidus and, in the second stage, the response to the application of synthetic desmopressin confirms a central origin.Because CDI is rare in felines, the aim of this study was to report the occurrence of a case of CDI, probably of congenitalprimary origin, in an 8-month-old kitten.Case: An 8-month-old male feline, castrated, 3.2 kg, was brought to consultation with a report of polydipsia, polyuria,smaller size and weight, and lower activity when compared to his brother, for several months. On physical examination,lethargy, body score 2/5, and mild dehydration were noted, as well as deciduous teeth that should have already been replaced. Abdominal ultrasound and laboratory tests were requested, which ruled out chronic kidney disease (CKD), diabetesmellitus (DM), hyperadrenocorticism (HAC), and hyperthyroidism. Due to the fact that urinalysis evidenced hyposthenuria(urinary density [UD] 1.004), CDI was suspected. The patient underwent a water deprivation test and, after 7.5 h, lost4.7% of his initial weight, while UD was 1.012, confirming the diagnosis of DI. The investigation then proceeded to theevaluation of the response to synthetic desmopressin by the application of 5 U IM. Two h later, UD was 1.019, confirming...(AU)

Evidence of pituitary hypoplasia associated with partial central diabetes insipidus in a young Persian cat

Background: Congenital anomalies are an uncommon pituitary hypofunction cause associated to multiple hormone deficiencies. Congenital hyposomatotropism is often related to an inherited anomaly, characterized mainly by delayed growth. It is not uncommon to find associated thyroid-stimulating hormone and gonadotropin deficiencies. Pituitary malformation may be associated to progressive cystic lesion expansion. Central diabetes insipidus (CDI) is another rare disease associated to polyuria (PU) and polydipsia (PD) secondary to antidiuretic hormone (ADH) deficient secretion. The aim of this report is to describe a likely case of pituitary hypoplasia, associated with partial CDI in a cat. Case: A 9-month-old unneutered male Persian cat weighing 2 kg was presented due to severe polyuria and polydipsia associated with growth deficit when compared with its sibling. After clinical and laboratory evaluations during the months in which the patient was monitored, reduced serum concentration of insulin-like growth factor-1 (IGF-1), thyroid-stimulating hormone (TSH), thyroid hormones, and testosterone were documented, confirming the diagnosis of hyposomatotropism, hypogonadism, and secondary hypothyroidism. Furthermore, therapeutic diagnosis with desmopressin revealed partial central diabetes insipidus (CDI). As the sibling showed normal development aging 13-months, a radiographic examination of the forelimb (carpus) was performed on both cats. There was lack of growth plate fusion in the patient, without any other evidence of dysgenesis, whereas complete epiphyseal closure was observed in the sibling. Despite therapeutic prescriptions of desmopressin and levothyroxine, the owners refused further follow-up to the...

Evidence of pituitary hypoplasia associated with partial central diabetes insipidus in a young Persian cat

Background: Congenital anomalies are an uncommon pituitary hypofunction cause associated to multiple hormone deficiencies. Congenital hyposomatotropism is often related to an inherited anomaly, characterized mainly by delayed growth. It is not uncommon to find associated thyroid-stimulating hormone and gonadotropin deficiencies. Pituitary malformation may be associated to progressive cystic lesion expansion. Central diabetes insipidus (CDI) is another rare disease associated to polyuria (PU) and polydipsia (PD) secondary to antidiuretic hormone (ADH) deficient secretion. The aim of this report is to describe a likely case of pituitary hypoplasia, associated with partial CDI in a cat. Case: A 9-month-old unneutered male Persian cat weighing 2 kg was presented due to severe polyuria and polydipsia associated with growth deficit when compared with its sibling. After clinical and laboratory evaluations during the months in which the patient was monitored, reduced serum concentration of insulin-like growth factor-1 (IGF-1), thyroid-stimulating hormone (TSH), thyroid hormones, and testosterone were documented, confirming the diagnosis of hyposomatotropism, hypogonadism, and secondary hypothyroidism. Furthermore, therapeutic diagnosis with desmopressin revealed partial central diabetes insipidus (CDI). As the sibling showed normal development aging 13-months, a radiographic examination of the forelimb (carpus) was performed on both cats. There was lack of growth plate fusion in the patient, without any other evidence of dysgenesis, whereas complete epiphyseal closure was observed in the sibling. Despite therapeutic prescriptions of desmopressin and levothyroxine, the owners refused further follow-up to the...(AU)

Central Diabetes insipidus in a cat

Background: Diabetes insipidus is a rare disease in cats with few reports in the scientifi c literature. It has two major forms: Central Diabetes Insipidus (CDI); characterized by decreased secretion of antidiuretic hormone (ADH), and Nephrogenic Diabetes Insipidus (NDI); characterized by decreased ability to concentrate urine because of resistance to ADH. The diagnosis is based on excluding diseases with polydipsia/polyuria, the water deprivation test and response to desmopressin. This case report describes Central Diabetes Insipidus in a domestic cat, as well as its response to desmopressin administered intranasally. Case: A 2-year old, male cat of non-defi ned breed and castrated was seen due to a history of polyuria and polydipsia (PU/ PD) that arose after allegedly ingesting thorns that got stuck to its body while going out of the house. Physical examination revealed an active well-fed animal with mild dehydration and persistent paradoxical ischuria. The complementary tests performed: abdominal ultrasound, blood test, urinalysis, serum urea, creatinine, glucose, cortisol, total T4, Total T3 and vasopressin, were within the reference values, except for urinary density and T4 that were below the standard. Based on the laboratory results, conditions compatible with PU and PD symptoms were excluded; however, despite normal vasopressin levels, diabetes insipidus was not ruled...(AU)

Central Diabetes insipidus in a cat

Background: Diabetes insipidus is a rare disease in cats with few reports in the scientifi c literature. It has two major forms: Central Diabetes Insipidus (CDI); characterized by decreased secretion of antidiuretic hormone (ADH), and Nephrogenic Diabetes Insipidus (NDI); characterized by decreased ability to concentrate urine because of resistance to ADH. The diagnosis is based on excluding diseases with polydipsia/polyuria, the water deprivation test and response to desmopressin. This case report describes Central Diabetes Insipidus in a domestic cat, as well as its response to desmopressin administered intranasally. Case: A 2-year old, male cat of non-defi ned breed and castrated was seen due to a history of polyuria and polydipsia (PU/ PD) that arose after allegedly ingesting thorns that got stuck to its body while going out of the house. Physical examination revealed an active well-fed animal with mild dehydration and persistent paradoxical ischuria. The complementary tests performed: abdominal ultrasound, blood test, urinalysis, serum urea, creatinine, glucose, cortisol, total T4, Total T3 and vasopressin, were within the reference values, except for urinary density and T4 that were below the standard. Based on the laboratory results, conditions compatible with PU and PD symptoms were excluded; however, despite normal vasopressin levels, diabetes insipidus was not ruled...

Diabetes insípido em um cão

Background: Diabetes insipidus (DI) is a rare endocrine disorder in dogs altering the mechanism of retention and excretion of water, with concomitant polyuria and polydipsia (PU/PD), and low urine specifi c gravity. The water deprivation test followed by response to application of desmopressin is the diagnostic test for the disease. However, the literature is still scarce about laboratorial and clinical aspects of DI in small animals. Thus, the aim of this study is to report a case of DI in a canine, emphasizing its diagnosis through the water deprivation test.Case: A male mongrel dog, 5 years-old, not neutered, 13kg of body weight, was presented with intense PU/PD (500mL/kg/day of water consumption). Physical examination showed normal routine clinical parameters. Additional tests were asked (abdominal ultrasound, blood count, serum biochemical (creatinine, alanine aminotransferase (ALT), total cholesterol, alkaline phosphatase (ALP) and glucose) and dexamethasone suppression test), but they showed no signifi cant changes. Thus, it was suspected that the animal had an uncommon endocrinopathy, DI. For its confi rmation, it was made the water deprivation test with application of desmopressin acetate. The patient remained without access to water and without fluidtherapy with urethral sounding and bladder emptying. The measurement of urinary gravity and volume were made every hour

Diabetes insípido em um cão / Diabetes Insipidus in a Dog

Background: Diabetes insipidus (DI) is a rare endocrine disorder in dogs altering the mechanism of retention and excretion of water, with concomitant polyuria and polydipsia (PU/PD), and low urine specific gravity. The water deprivation test followed by response to application of desmopressin is the diagnostic test for the disease. However, the literature is still scarce about laboratorial and clinical aspects of DI in small animals. Thus, the aim of this study is to report a case of DI in a canine, emphasizing its diagnosis through the water deprivation test. Case: A male mongrel dog, 5 years-old, not neutered, 13kg of body weight, was presented with intense PU/PD (500mL/kg/day of water consumption). Physical examination showed normal routine clinical parameters. Additional tests were asked (abdominal ultrasound, blood count, serum biochemical (creatinine, alanine aminotransferase (ALT), total cholesterol, alkaline phosphatase (ALP) and glucose) and dexamethasone suppression test), but they showed no significant changes. Thus, it was suspected that the animal had an uncommon endocrinopathy, DI. For its confirmation, it was made the water deprivation test with application of desmopressin acetate. The patient remained without access to water and without fluidtherapy with urethral sounding and bladder emptying. The measurement of urinary gravity and volume were made every hour for 12 h. After 8 h from the start of the test, it was made the application of desmopressin acetate (three drops in the conjunctival sac), because the animal began to exhibit tremors and muscle weakness (urine specific gravity: 1005). In this period, their body weight decreased 11.6%. After application of desmopressin, urine specific gravity increased gradually every hour, ending with urine specific gravity measurements of 1023, confirming the diagnosis of central DI. Discussion: The diagnosis of DI can be a challenge to the veterinary practitioner since it is a rare disease in small animals, and often is not included in the differential diagnoses. Furthermore, additional tests such as common hematological, biochemical and electrolyte profiles usually have normal results, or secondary influences of dehydration. The water deprivation test confirms the inability of the animal to concentrate urine in DI. However, this test is potentially dangerous because of the serious consequences of dehydration, requiring constant monitoring. In DI of central origin (DIC), the urinary concentration usually starts 1 to 3 h after administration of desmopressin acetate, and tends to be within the normal reference value, as can be observed in this case. Because there were not neurological signs, the final diagnosis of the animal was acquired DIC. DIC is acquired by the destruction of cells of supraoptic and paraventricular nuclei of the hypothalamus, or even, loss of the ducts that carry the anti-diuretic hormone (ADH) by the pituitary for secretion and storage. Desmopressin acetate (dDAVP), a synthetic analogue of vasopressin, was used for the initial treatment (three drops in the conjunctival sac, once a day) which controlled the PU/PD of the animal. After four months of treatment initiation, the animal has moved to a drop of the drug, twice a day. The dog of the present case has reported good prognosis, since small animals with acquired DIC become relatively asymptomatic in response to appropriate therapy.

Diabete insípido central em um cão

A case of central diabetes insipidus in a nine-year-old female dog is described. The dog presented intermitent polyuria and polydipsia in the past 18 months. In the clinical exam, complete blood count, alanine transaminase, alkaline phosphatase, BUN, creatinine, glucose and calcium dosages were normal. However, the specific urine gravity was low and presented the value 1002. The dog was unable to concentrate the urine during the seven hours of water deprivation test and presented 5% of dehydratation. The administration of desmopressin acetate elevated the specific urine gravity to 1028 five hours after the beginning of the treatment, confirming the diagnosis of diabetes insipidus of central origin.

Descreve-se um caso de diabete insípido central em um cão, fêmea, nove anos de idade, sem raça definida, com história de poliúria e polidipsia há 18 meses. Com o exame físico, nenhuma alteração sistêmica foi elucidada. Já nos exames laboratoriais complementares, observou-se policitemia e hiperproteinemia, e a densidade específica da urina (1002) encontrava-se abaixo do limiar fisiológico. O animal foi submetido à privação hídrica e se mostrou incapaz de concentrar a urina durante as sete horas observadas, tempo que levou para apresentar 5% de desidratação. Após isso, foi administrado acetato de desmopressina e, 5 horas após, a densidade estava em 1028, confirmando o diabete insípido de origem central. O animal recebeu terapia à base de acetato de desmopressina, apresentando melhora do quadro clínico.

Diabete insípido central em um cão

A case of central diabetes insipidus in a nine-year-old female dog is described. The dog presented intermitent polyuria and polydipsia in the past 18 months. In the clinical exam, complete blood count, alanine transaminase, alkaline phosphatase, BUN, creatinine, glucose and calcium dosages were normal. However, the specific urine gravity was low and presented the value 1002. The dog was unable to concentrate the urine during the seven hours of water deprivation test and presented 5% of dehydratation. The administration of desmopressin acetate elevated the specific urine gravity to 1028 five hours after the beginning of the treatment, confirming the diagnosis of diabetes insipidus of central origin.

Descreve-se um caso de diabete insípido central em um cão, fêmea, nove anos de idade, sem raça definida, com história de poliúria e polidipsia há 18 meses. Com o exame físico, nenhuma alteração sistêmica foi elucidada. Já nos exames laboratoriais complementares, observou-se policitemia e hiperproteinemia, e a densidade específica da urina (1002) encontrava-se abaixo do limiar fisiológico. O animal foi submetido à privação hídrica e se mostrou incapaz de concentrar a urina durante as sete horas observadas, tempo que levou para apresentar 5% de desidratação. Após isso, foi administrado acetato de desmopressina e, 5 horas após, a densidade estava em 1028, confirmando o diabete insípido de origem central. O animal recebeu terapia à base de acetato de desmopressina, apresentando melhora do quadro clínico.

Acompanhamento laboratorial da função renal de cães sadios tratados experimentalmente com doses terapêuticas de anfotericina B

The objective of this experiment was to assess the renal function of ten healthy male adult dogs submitted to therapeutic doses of amphotericin B, whose use has been limited due to its high nephrotoxic potential, as well as to evaluate the more sensitive and early method to diagnose kidney lesions. The renal function was evaluated through daily urinalysis, fractioned excretion of sodium and potassium, serum concentration of creatinine and blood urea nitrogen (BUN) and urinary activity of gamma-glutamyltransferase (GGT). It was concluded that amphotericin b provokes lesions in both proximal and distal tubules, inducing type I renal tubular acidosis and nephrogenic Diabetes insipidus in dogs. Renal function evaluation, preferably by serum creatinine, BUN and potassium dosage is recommended before each drug application. Urinalysis proved to diagnose kidney lesions in its earliest stage through a modification of the density parameters. Urinary GGT was not effective as an earliest diagnose kidney lesions caused by amphotericin B.

O presente trabalho objetivou avaliar a função renal de dez cães adultos saudáveis submetidos à administração de doses terapêuticas do antifúngico anfotericina B, cuja utilização tem sido limitada pelo seu elevado potencial nefrotóxico, e avaliar o método laboratorial mais sensível e precoce de diagnóstico de lesão renal. Foram realizadas, diariamente, urinálise, excreção fracionada de sódio e potássio, dosagem sérica de creatinina e uréia e atividade urinária de gama-glutamiltransferase (GGT). Concluiu-se que a anfotericina B provoca lesões nos túbulos proximal e distal, induzindo acidose tubular renal do tipo I e Diabetes insipidus nefrogênico em cães. Avaliação da função renal, preferencialmente por dosagens de creatinina, uréia e potássio séricos, é recomendada antes de cada aplicação do fármaco. A densidade urinária foi o parâmetro mais precocemente alterado pela lesão renal. A GGT urinária não foi eficaz para o diagnóstico precoce de lesão induzida por anfotericina B.

Acompanhamento laboratorial da função renal de cães sadios tratados experimentalmente com doses terapêuticas de anfotericina B

The objective of this experiment was to assess the renal function of ten healthy male adult dogs submitted to therapeutic doses of amphotericin B, whose use has been limited due to its high nephrotoxic potential, as well as to evaluate the more sensitive and early method to diagnose kidney lesions. The renal function was evaluated through daily urinalysis, fractioned excretion of sodium and potassium, serum concentration of creatinine and blood urea nitrogen (BUN) and urinary activity of gamma-glutamyltransferase (GGT). It was concluded that amphotericin b provokes lesions in both proximal and distal tubules, inducing type I renal tubular acidosis and nephrogenic Diabetes insipidus in dogs. Renal function evaluation, preferably by serum creatinine, BUN and potassium dosage is recommended before each drug application. Urinalysis proved to diagnose kidney lesions in its earliest stage through a modification of the density parameters. Urinary GGT was not effective as an earliest diagnose kidney lesions caused by amphotericin B.

O presente trabalho objetivou avaliar a função renal de dez cães adultos saudáveis submetidos à administração de doses terapêuticas do antifúngico anfotericina B, cuja utilização tem sido limitada pelo seu elevado potencial nefrotóxico, e avaliar o método laboratorial mais sensível e precoce de diagnóstico de lesão renal. Foram realizadas, diariamente, urinálise, excreção fracionada de sódio e potássio, dosagem sérica de creatinina e uréia e atividade urinária de gama-glutamiltransferase (GGT). Concluiu-se que a anfotericina B provoca lesões nos túbulos proximal e distal, induzindo acidose tubular renal do tipo I e Diabetes insipidus nefrogênico em cães. Avaliação da função renal, preferencialmente por dosagens de creatinina, uréia e potássio séricos, é recomendada antes de cada aplicação do fármaco. A densidade urinária foi o parâmetro mais precocemente alterado pela lesão renal. A GGT urinária não foi eficaz para o diagnóstico precoce de lesão induzida por anfotericina B.

Diabetes insipidus central em um gato: relato de caso / Central diabetes insipidus in a cat: case report

O diabetes insípidus é uma enfermidade rara nos animais domésticos caracterizada por uma intensa poliúria e polidipsia secundária. Um gato foi examinado com a principal queixa de poliúra e polidipsia. O diagnóstico de diabetes insipidus central foi baseado em uma hipostenúria persistente com incapacidade de concentrar urina em resposta à privação hídrica e numa resposta positiva após a administração exógena do hormônio antidiurético. O tratamento com a DDAVP (1 desamino-8-D-arginina vasopressina) administrado no saco conjuntival a cada 12 horas controlou os sintomas(AU)

Diabetes insipidus is a rare disease of animals characterized by diuresis of dilute urine, with secondary polydipsia. A 1 year-old, male cat was presented for examination because polyuria and polydipsia. Central diabetes insipidus was diagnosed, based on persistent hyposthenuria with failure to concentrate urine in response to water deprivation and positive response to antidiuretic hormone administration. Treatment with DDAVP (1 desamino-8-D-arginine vasopressin) given in the conjunctival sac every 12 hours controlled the symptoms(AU)

Diabetes insipidus central em um gato: relato de caso / Central diabetes insipidus in a cat: case report

O diabetes insípidus é uma enfermidade rara nos animais domésticos caracterizada por uma intensa poliúria e polidipsia secundária. Um gato foi examinado com a principal queixa de poliúra e polidipsia. O diagnóstico de diabetes insipidus central foi baseado em uma hipostenúria persistente com incapacidade de concentrar urina em resposta à privação hídrica e numa resposta positiva após a administração exógena do hormônio antidiurético. O tratamento com a DDAVP (1 desamino-8-D-arginina vasopressina) administrado no saco conjuntival a cada 12 horas controlou os sintomas

Diabetes insipidus is a rare disease of animals characterized by diuresis of dilute urine, with secondary polydipsia. A 1 year-old, male cat was presented for examination because polyuria and polydipsia. Central diabetes insipidus was diagnosed, based on persistent hyposthenuria with failure to concentrate urine in response to water deprivation and positive response to antidiuretic hormone administration. Treatment with DDAVP (1 desamino-8-D-arginine vasopressin) given in the conjunctival sac every 12 hours controlled the symptoms

Diabetes insípido em um cão

Background: Diabetes insipidus (DI) is a rare endocrine disorder in dogs altering the mechanism of retention and excretion of water, with concomitant polyuria and polydipsia (PU/PD), and low urine specifi c gravity. The water deprivation test followed by response to application of desmopressin is the diagnostic test for the disease. However, the literature is still scarce about laboratorial and clinical aspects of DI in small animals. Thus, the aim of this study is to report a case of DI in a canine, emphasizing its diagnosis through the water deprivation test.Case: A male mongrel dog, 5 years-old, not neutered, 13kg of body weight, was presented with intense PU/PD (500mL/kg/day of water consumption). Physical examination showed normal routine clinical parameters. Additional tests were asked (abdominal ultrasound, blood count, serum biochemical (creatinine, alanine aminotransferase (ALT), total cholesterol, alkaline phosphatase (ALP) and glucose) and dexamethasone suppression test), but they showed no signifi cant changes. Thus, it was suspected that the animal had an uncommon endocrinopathy, DI. For its confi rmation, it was made the water deprivation test with application of desmopressin acetate. The patient remained without access to water and without fluidtherapy with urethral sounding and bladder emptying. The measurement of urinary gravity and volume were made every hour

Acompanhamento laboratorial da função renal de cães sadios tratados experimentalmente com doses terapêuticas de anfotericina b

A presença de uma função renal adequada é importante para a manutenção da homeostase. A anfotericina b é um antifúngico potente, cuja utilização tem sido limitada devido ao seu elevado potencial nefrotóxico. O presente trabalho teve por objetivos acompanhar, laboratorialmente, a função renal de cães saudáveis submetidos à administração de doses terapêuticas do antifúngico anfotericina b (FungisonÒ), bem como avaliar dentre os métodos laboratoriais empregados, qual o método mais sensível e precoce de diagnóstico de lesão renal. A função renal foi avaliada por meio da realização diária de urinálise, da excreção fracionada dos eletrólitos sódio e potássio, dosagem das concentrações séricas de creatinina e uréia e atividade da enzima gama-glutamiltransferase (GGT) urinária. Cada animal foi seu próprio controle, uma vez que foram obtidas amostras de urina e sangue de cada animal, para realização dos exames acima citados, antes da primeira aplicação do fármaco. Concluiu-se que a anfotericina b provoca lesões tanto em túbulo proximal quanto em distal, onde a alteração em túbulo distal foi a primeira a ser detectada, por meio da diminuição dos valores de densidade urinária; dosagem de creatinina e uréia séricas e potássio sérico, deve ser realizada antes de cada aplicação do fármaco; a enzima urinária gama-glutamiltrasferase (GGT) não foi eficaz como método de diagnóstico de lesão renal induzida por anfotericina b; demonstrou-se também que a anfotericina b provoca acidose tubular renal do tipo I e induz diabetes insipidus nefrogênico em cães

Anfotericina B is a strong anti-fungus agent, which use has been limited due to its high nephrotoxic potential. The objective of this experiment is to accompany in the laboratory the renal function of healthy dogs which were submitted to therapeutic doses of Anfotericina B (Fungison®), as well as to evaluate which method can first diagnose kidney lesions with the most precise results. Ten healthy adult male dogs were used in the experiment. All dogs received five doses of 0.5 mg/kg of Anfotericina B every other day. The renal function was evaluated through daily urine exams, fractioned excretion of the electrolytes sodium and potassium, doses of serical concentrations of creatine and urea and the activity of the enzyme gama-glutamiltransferase (GGT) [urinaria]. Throughout the experiment, each animal was individually tested. We concluded that Anfoteracina B provokes lesions both in the proximal and distal tubes. Urinalysis proved to diagnose kidney lesions in its earliest stage through a modification of the density parameters. The dosage of creatine and serical urea must be effected before each application of Anfoteracina B. Finally, urinal enzyme gama-glutamiltrasferase (GGT) should not be used as a method to diagnose kidney lesions caused by therapeutic doses of Anfotericina B. The experiment also demonstrates the importance of accompanying the serical concentration of potassium during the treatment with Anfotericina B. Finally, we concluded that Anfotericina B resulted in tubular acidosis type I of the kidney, as well as induces nephrogenic diabetes insipidus in dogs