Abstract-Effect of progesterone (1 mg/kg) on the inflammation in rats induced by carrageenin was studied. Progesterone inhibited the vascular permeability and the formation of granulation tissue in the early phase of the inflammation.In the chronic proliferative phase, progesterone suppressed the vascular permeability and there was an active resorption of the granulation tissue. Increased degradation of noncollagen protein was observed in the treated group without apparent influence on the metabolism of collagen or on the synthesis of noncollagen protein. It is important, therefore, to determine how progesterone in fluences the entire course of acute and chronic phases of the inflammatory processes. The present experiment was undertaken in an attempt to determine the influence of progesterone on carrageenin-induced inflammation.We used the carrageenin-air-pouch method which was developed as an experimental model covering not only acute exudative but also chronic proliferative stages of the inflammatory processes (4).
MATERIALS AND METHODSAn inflammation in the form of carrageenin-air-pouch was induced on the back of male Donryu rats according to the procedure of Tsurufuji et al. (4). In rats weighing 130-160 g, 7 ml of air was injected s.c. on the back to make an air pouch. After 24 hr, 4.0 ml of 2 (w/v) % solution of Seakem 202 carrageenin (Marine Colloid Inc., Springfield, N.J., U.S.A.) was injected into the air pouch already formed. Radioiodinated human serum albumin (131I-HSA, Dainabot Co., Tokyo, 5 ttCi /mg) was used after purification by gel filtration as an indicator for the measurement of vascular permeability (5). 131I-HSA (4 ,nCi/kg in I ml of 0.9 % NaCI) was given i.v. 4 hr after the last injection of progesterone, and 30 min later the rats were sacrificed by cutting carotid artery. The entire exudate and the pouch of the granulation tissue were harvested. The exudate was centrifuged at 2,000 x g for 10 min at 4'C. The radioactivity of the supernatant (1 ml) was measured in a well type scintillation spectrometer as described in a previous paper (5). Total radioactivity in the entire pouch fluid of each rat was calculated and expressed in terms of the percentage of the radioactivity injected and used as an index of the vascular permeability of the inflamed tissue.Collagen of the granulation tissue was extracted as gelatin by autoclaving the tissue with distilled water. The extraction was done twice and the resulting collagen-free residue was referred to as the noncollagen protein fraction. The amounts and the radioactivities of collagen and noncollagen protein fractions were measured according to the procedure described previously (6). Briefly, collagen extracted as gelatin was hydrolyzed with 6 N HCI at 105'C for 16 hr. The amount of hydroxyproline in the hydrolysate was measured by the method of Kivirikko et al. (7). The radioactivity of hydroxyproline in the hydrolysate was measured after converting hydroxyproline into pyrrole which was purified by passing through a silicic acid column. The purified...