Aldose reductase inhibition prevents galactose-induced ovarian dysfunction in the Sprague-Dawley rat. 1992

W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
Yale-New Haven Hospital, Yale University School of Medicine, New Haven, Connecticut.

OBJECTIVE Our objective was to determine whether impaired ovarian function induced by short-term creation of a galactosemic state in the rat might be prevented by the coadministration of an aldose reductase inhibitor. METHODS Prepubertal Sprague-Dawley rats were fed four different diets including (1) control, (2) 40% galactose, (3) 40% galactose and an aldose reductase inhibitor, and (4) an aldose reductase inhibitor with the control diet. Percentage germinal vesicle breakdown, postovulatory oocyte quantities, hormonal parameters, ovarian histologic evaluation, and ovarian galactitol concentrations were determined. RESULTS The galactose-fed animals (group 2) had decreased germinal vesicle breakdown (47%) versus control (69%, p < 0.05). Galactose-exposed animals had significantly decreased quantities of postovulatory eggs (6.4 per animal) after menotropin ovarian stimulation in comparison with controls (14.1, p < 0.01). In rats exposed to high dietary levels of galactose (group 2) ovarian galactitol concentrations were significantly higher (protein 42.12 mumol/gm versus 0.0 for controls, p < 0.005). When galactose-fed animals received the aldose reductase inhibitor, ovarian accumulation of galactitol was significantly reduced and the observed detrimental effects on the oocyte were prevented. CONCLUSIONS Galactitol accumulation or metabolic flux through aldose reductase in galactosemic rodents may be involved in the demonstrated ovarian dysfunction.

UI MeSH Term Description Entries
D010049 Ovarian Diseases Pathological processes of the OVARY. Disease, Ovarian,Diseases, Ovarian,Ovarian Disease
D010053 Ovary The reproductive organ (GONADS) in female animals. In vertebrates, the ovary contains two functional parts: the OVARIAN FOLLICLE for the production of female germ cells (OOGENESIS); and the endocrine cells (GRANULOSA CELLS; THECA CELLS; and LUTEAL CELLS) for the production of ESTROGENS and PROGESTERONE. Ovaries
D004376 Galactitol A naturally occurring product of plants obtained following reduction of GALACTOSE. It appears as a white crystalline powder with a slight sweet taste. It may form in excess in the lens of the eye in GALACTOSEMIAS, a deficiency of GALACTOKINASE. Dulcitol
D005260 Female Females
D005690 Galactose An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. D-Galactose,Galactopyranose,Galactopyranoside,D Galactose
D006107 Granulosa Cells Supporting cells for the developing female gamete in the OVARY. They are derived from the coelomic epithelial cells of the gonadal ridge. Granulosa cells form a single layer around the OOCYTE in the primordial ovarian follicle and advance to form a multilayered cumulus oophorus surrounding the OVUM in the Graafian follicle. The major functions of granulosa cells include the production of steroids and LH receptors (RECEPTORS, LH). Cell, Granulosa,Cells, Granulosa,Granulosa Cell
D000449 Aldehyde Reductase An enzyme that catalyzes reversibly the oxidation of an aldose to an alditol. It possesses broad specificity for many aldoses. EC 1.1.1.21. Aldose Reductase,Aldose Reductase Ia,Aldose Reductase Ib,Erythrose Reductase,Xylose Reductase,Reductase Ia, Aldose,Reductase Ib, Aldose,Reductase, Aldehyde,Reductase, Aldose,Reductase, Erythrose,Reductase, Xylose
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D017207 Rats, Sprague-Dawley A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company. Holtzman Rat,Rats, Holtzman,Sprague-Dawley Rat,Rats, Sprague Dawley,Holtzman Rats,Rat, Holtzman,Rat, Sprague-Dawley,Sprague Dawley Rat,Sprague Dawley Rats,Sprague-Dawley Rats
D051381 Rats The common name for the genus Rattus. Rattus,Rats, Laboratory,Rats, Norway,Rattus norvegicus,Laboratory Rat,Laboratory Rats,Norway Rat,Norway Rats,Rat,Rat, Laboratory,Rat, Norway,norvegicus, Rattus

Related Publications

W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
October 2007, Investigative ophthalmology & visual science,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
August 1987, Environmental health perspectives,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
December 2015, Chemistry & biodiversity,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
May 2014, Investigative ophthalmology & visual science,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
April 1995, Diabetologia,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
April 2018, Biochemical pharmacology,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
August 2011, Carcinogenesis,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
January 1993, Japanese journal of ophthalmology,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
April 2004, Diabetologia,
W R Meyer, and M B Doyle, and J A Grifo, and K J Lipetz, and P J Oates, and A H DeCherney, and M P Diamond
June 1989, The American journal of physiology,
Copied contents to your clipboard!