The Role of Dyslipidemia on Ocular Surface, Lacrimal and Meibomian Gland Structure and Function


Autoria(s): Modulo, Carolina Maria; Machado Filho, Elisio Bueno; Malki, Leonardo Tannus; Dias, Ana Carolina; de Souza, Jane Cristina; Oliveira, Helena C. F.; Jorge, Italo Cade; Santos Gomes, Isabele Beserra; Meyrelles, Silvana S.; Rocha, Eduardo Melani
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

21/10/2013

21/10/2013

2012

Resumo

Purpose: Dyslipidemia is characterized by high lipid blood levels that are risk factors for cardiovascular diseases, which are leading causes of death. However, it is unclear whether dyslipidemia is a cause of the dry eye syndrome (DES). Therefore we determined in transgenic mice models of dyslipidemia, whether there is an association with DES development. Methods: Dyslipidemic models included male and female adult mice overexpressing apolipoprotein CIII (Apo CIII), LDL receptor knockout (LDLR-KO) and ApoE knockout (ApoE-KO). They were compared with age-and gender-matched C57BL/6 mice. Ocular health was evaluated based on corneal slit lamp assessment, phenol red thread test (PRT) and impression cytology. Blood lipid profiles and histology of meibomian and lacrimal glands were also evaluated. Effects of high-fat diet and aging were observed in LDLR-KO and ApoCIII strains, respectively. Results: Body weight and lacrimal gland weight were significantly higher in male mice compared to females of the same strain (P < 0.05). Body weight was significantly lower in LDLRKO mice receiving high lipid diet compared to their controls (P = 0.0043). ApoE-KO were hypercholesterolemic and ApoCIII hypertriglyceridemic while LDLR-KO showed increases in both parameters. The PRT test was lower in male LDLR-KO mice with high-fat diet than control mice with standard diet (P = 0.0273). Aging did not affect lacrimal structural or functional parameters of ApoCIII strain. Conclusions: DES development is not solely dependent on dyslipidemia in relevant mice models promoting this condition. On the other hand, lacrimal gland structure and function are differentially impacted by lipid profile changes in male and female mice. This dissociation suggests that other factors beside dyslipidemia impact on tear film dysfunction and DES development.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Fundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto da Universidade de Sao Paulo (FAEPA)

Fundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto da Universidade de Sao Paulo (FAEPA)

Identificador

CURRENT EYE RESEARCH, LONDON, v. 37, n. 4, supl. 1, Part 1, pp. 300-308, APR, 2012

0271-3683

http://www.producao.usp.br/handle/BDPI/35392

10.3109/02713683.2011.631720

http://dx.doi.org/10.3109/02713683.2011.631720

Idioma(s)

eng

Publicador

INFORMA HEALTHCARE

LONDON

Relação

CURRENT EYE RESEARCH

Direitos

restrictedAccess

Copyright INFORMA HEALTHCARE

Palavras-Chave #APOLIPOPROTEIN #LOW DENSITY LIPOPROTEIN #LACRIMAL GLAND #MEIBOMIAN GLAND #DRY EYE #OCULAR SURFACE #DRY EYE #ANDROGEN DEFICIENCY #SJOGRENS-SYNDROME #TRANSGENIC MICE #TEAR FILM #CHOLESTEROL #LIPOPROTEIN #DISEASE #ATHEROSCLEROSIS #HYPERLIPIDEMIA #OPHTHALMOLOGY
Tipo

article

original article

publishedVersion