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Experimental Biology and Medicine

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Exp. Biol. Med. 2009;234:562-565
doi:10.3181/0811-BC-341
© 2009 Society for Experimental Biology and Medicine

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ORIGINAL RESEARCH ARTICLE

The Source and Secretion of Immunoactive Relaxin in Rat Milk

Bernard G. Steinetz1, Lori Horton and Sally Lasano

Department of Environmental Medicine, NYU School of Medicine, Tuxedo, New York 10987

1 NYU School of Medicine, Nelson Institute of Environmental Medicine, 57 Old Forge Road, Tuxedo, NY 10987. E-mail: bernard.steinetz{at}nyumc.org

The milk of many mammalian species contains hormones and growth factors in addition to nutrients and immuocompetent substances. These factors can be absorbed into the circulation of suckling neonates to exert important effects on metabolism and promote tissue and organ growth. Frequently, there is uncertainty as to whether such substances are gene products of the mammary glands themselves or are produced elsewhere and concentrated from the systemic circulation. The 6 kD polypeptide, relaxin, appears in milk of several mammalian species, including that of the rat, but proof of its source of secretion (corpus luteum vs. mammary gland) is so far lacking. The specific monoclonal anti-rat relaxin antibody MCA1 has previously been utilized successfully to investigate many of relaxin’s actions in the rat, including those affecting the development of the mammary apparatus. In this report, MCA1 was utilized to aid in the identification of the source of relaxin in rat milk. Treatment of lactating rats with MCA1 completely neutralized the luteal relaxin circulating in serum but did not decrease the concentration of immunoactive relaxin secreted in milk. Moreover, the antibody did not appear to reach the mammary epithelium. The evidence thus supports the view that in the rat, the relaxin secreted in milk is primarily a product of the mammary glands and not concentrated from the systemic circulation.

Keywords: milk-borne relaxin (or lactocrine relaxin), neutralizing antibody, mammary glands, lactating rats

This work was supported in part by grants from the Cancer Research Foundation of America and by NYU NIEHS Center Grant ES00260.


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