Abstract
LH [luteinizing hormone] from rat anterior pituitary and serum was characterized with respect to its molecular size, and immunological and biological activity. Pituitary extracts prepared by homogenization followed by high speed centrifugation and chromatography on Ultrogel (AcA 44, 1.5 .times. 80 cm) columns showed 2 peaks of radioimmunoassayable LH activity, a major peak 1 and a minor peak 2. On the basis of their elution from Ultrogel columns, peak 1 had a larger molecular size (Kav = 0.44) than peak 2 (Kav = 0.53). The biological activities of the 2 peaks were assessed by testing the ability of the 2 peaks to stimulate cAMP production and progesterone synthesis using immature rat ovarian cells. Both cAMP production and progesterone synthesis by ovarian cells were stimulated by peak 1 and peak 2 in a dose dependent manner, but differed in the degree of stimulation. At optimal concentrations, stimulation of cAMP production by peak 2 was 1.45-fold higher than peak 1. Similarly, stimulation of progesterone production by peak 2 was 2-fold higher than that produced by peak 1. The molecular size of the LH released from anterior hemipituitaries in response to a gonadoliberin (luliberin, LRH) agonist, [Des-gly-NH210]LRH ethylamide, was also determined. Chromatography of control medium as well as the agonist treated medium on the Ultrogel columns showed a single peak of LH activity at a position which corresponded to peak 1 found in the pituitary extract. The elution profile of serum LH from animals injected with LRH agonist was similar to that of peak 2 of the pituitary extract. Incubation of the pituitary extract with serum resulted in a shift in the position of elution of peak 1 towards peak 2. The anterior pituitary apparently contains a major high MW form of LH with lower biological activity and a minor low MW form with higher biological activity, but only the low MW form appears in the circulation.

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