Slama-Scemama A, Noteborn H P, de Morée A, de Korte-Kool G M, Leblanc P, Gogan F, L'Héritier A, Ebels I
J Neural Transm. 1985;62(1-2):155-67. doi: 10.1007/BF01260424.
A high molecular weight fraction XM100R (MW A 100,000) was prepared by ultrafiltration from ovine pineals using two different extraction methods under red light conditions (lambda greater than 600 nm). This fraction stimulates the release of radioimmunologically active luteinizing hormone (LH) of anterior pituitaries in vitro. The ultrafiltration fraction PM30R (MW greater than 30,000 and less than 100,000) was found to be radioimmunologically active only when the "Bensinger" extraction procedure was applied. However, when comparable fractions were prepared under green light and incubated with half-pituitaries, all the incubation media of the ultrafiltrated fractions, XM100R, PM30R, PM10R (MW greater than 10,000 and less than 30,000) UM2R (MW greater than 1000 and less than 10,000), UM05R (MW greater than 500 and less than 1000) and UM05F (MW greater than 500), reacted with anti-LH. This may mean that under green light conditions the high molecular weight ovine pineal compounds in XM100R are disintegrated and/or split up into small molecules which can stimulate the release of LH, or crossreact with the anti-LH serum.
在红光条件下(波长大于600nm),使用两种不同的提取方法从绵羊松果体中通过超滤制备了一种高分子量组分XM100R(分子量约100,000)。该组分在体外可刺激垂体前叶释放具有放射免疫活性的促黄体生成素(LH)。仅当采用“本辛格”提取程序时,超滤组分PM30R(分子量大于30,000且小于100,000)才具有放射免疫活性。然而,当在绿光条件下制备可比组分并与半垂体一起孵育时,所有超滤组分XM100R、PM30R、PM10R(分子量大于10,000且小于30,000)、UM2R(分子量大于1000且小于10,000)、UM05R(分子量大于500且小于1000)和UM05F(分子量大于500)的孵育培养基均与抗LH发生反应。这可能意味着在绿光条件下,XM100R中的高分子量绵羊松果体化合物会分解和/或分裂成可刺激LH释放的小分子,或与抗LH血清发生交叉反应。