ABSTRACT
1. Evidence is presented for the occurrence of type 1 prostaglandin 15-hidroxydehydrogenase in human rectal mucosa. No evidence of the presence of type 2 dnzyme was found. 2. A 15-keto-prostaglandin reductase, responsible for the breakdown of 13, 14-dihydro 15-keto prostaglandins to 13, 14-dihydro prostaglandins, was also present in human rectal mucosa. 3. Ulcerative colitis patients catabolized prostaglandins to the same extent as the control group. PGE was catabolized significantly better than PGF2 alfa. 4. 5-Aminosalicylic acid and sulphapyridine did not affect prostaglandin catabolism. Sulphasalazine, methilsulphasalazine, indomethacin, flurbiprofen, disodium cromoglycate, sodium salicylate and carbenoxolone sodium inhibited prostaglandin catabolism to the same extent in both groups.Salicylazosulphadimidine was a more potent inhibitor of PGE1 catabolism than of PGF2alfa. 5. The increased prostaglandin synthesis reported for ulcerative colitis patients was not paralleled by increased catabolism, a fact possibly contributing to the accumulation of such compounds in the diseased state
Subject(s)
Adult , Middle Aged , Humans , Male , Female , Aminosalicylic Acids/pharmacology , Colitis, Ulcerative/metabolism , Prostaglandins E/metabolism , Prostaglandins F/metabolism , Sulfasalazine/pharmacology , Aminosalicylic Acids/therapeutic use , Colitis, Ulcerative/drug therapy , Intestinal Mucosa/pathology , NADP/metabolism , Sulfasalazine/therapeutic useABSTRACT
Several examples will be described in which powerful separation methods are combined with relatively simple chemical modification techniques to provide structural information on complex macromolecular assemblies. Ribosomal RNA structure has been examined by crosslinking, separating individual crosslinked species by gel electrophoresis, and enzymatic methods for determination of crosslink positions in the nucleotide sequence. Chromatin structure has been examined by footprinting the location of individual nucleosomes by a combination of chemical nicking and DNA separations. Virus structure can be examined by using breakable crosslinkers analyzed with diagonal gel electrophoresis. Ultimately such methods may allow structural information to be obtained on systems even as complex as whole chromosomes.