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   <subfield code="a">Systemic treatment with epidermal growth factor but not insulin-like growth factor I decreases the involution of the prostate in castrated rats</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Niels Tørring, Lars Vinter-Jensen, Flemming Brandt Sørensen, Allan Flyvbjerg, Ebba Nexø]</subfield>
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   <subfield code="a">Epidermal growth factor (EGF) and insulin-like growth factor I (IGF-I) are strong inducers of proliferation to prostate cells cultured in serum-free medium. Accordingly we wanted to study the growth of the prostate gland in castrated rats after treatment with EGF, IGF-I and testosterone. Castrated Wistar rats were treated with growth factors (EGF 35 μg/rat per day; IGF-I 350 μg/rat per day) or testosterone (2 mg/rat per day) for 3 days either immediately after or 10 days after castration. Prostate tissue was examined by stereological and immunohistochemical techniques and by enzyme-linked immunosorbent assay (ELISA). Treatment with EGF inhibited the involution of the prostate (P &lt; 0.05), whereas treatment with IGF-I did not affect the prostate involution as compared to castrated controls. EGF treatment significantly increased the endogenous rat EGF in the ventral prostate, but cellular proliferation was not affected. Testosterone treatment increased the weight of the prostate, by increase of all tissue components of the prostate, and significantly increased cellular proliferation. Systemic administration of EGF but not IGF-I decreased the involution of the rat prostate induced by castration. Compared with testosterone, the effects of EGF treatment on the prostate involution were moderate, and the effects of EGF were not related to cellular proliferation.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2000</subfield>
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   <subfield code="a">Key words Castration</subfield>
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   <subfield code="a">Epidermal growth factor</subfield>
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   <subfield code="u">Department of Clinical Biochemistry-KH, Aarhus University Hospital, Nørrebrogade 44, DK-8000 Aarhus C, Denmark e-mail: ntorring@hotmail.com Tel.: +45-8949-3082; Fax: +45-8949-3060, DK</subfield>
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   <subfield code="u">Department of Clinical Biochemistry-KH, Aarhus University Hospital, Nørrebrogade 44, DK-8000 Aarhus C, Denmark e-mail: ntorring@hotmail.com Tel.: +45-8949-3082; Fax: +45-8949-3060, DK</subfield>
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   <subfield code="u">Department of Clinical Biochemistry-KH, Aarhus University Hospital, Nørrebrogade 44, DK-8000 Aarhus C, Denmark e-mail: ntorring@hotmail.com Tel.: +45-8949-3082; Fax: +45-8949-3060, DK</subfield>
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   <subfield code="u">Department of Clinical Biochemistry-KH, Aarhus University Hospital, Nørrebrogade 44, DK-8000 Aarhus C, Denmark e-mail: ntorring@hotmail.com Tel.: +45-8949-3082; Fax: +45-8949-3060, DK</subfield>
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