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Thromboxane and prostacyclin synthesis following whole body irradiation in rats

Journal Article · · J. Appl. Physiol.: Respir., Environ. Exercise Physiol.; (United States)
OSTI ID:5751607

The effect of radiation on the mechanism and source of in vivo thromboxane B/sub 2/ (TxB/sub 2/) and 6-keto-prostaglandin F/sub 1..cap alpha../ (6-keto-PGF/sub 1..cap alpha..) synthesis was evaluated. Rats were irradiated with 2, 10, or 20 gray (Gy) whole body gamma irradiation and showed an increase in urine TxB/sup 2/ after either 10 or 20 Gy. Urine 6-keto-PGF/sub 1..cap alpha../ was elevated only after exposure to 20 Gy. Irradiation did not alter urine volume and osmolarity, nor was there a correlation between urine osmolarity and the urinary concentration of TxB/sup 2/ or 6-keto-PGF/sub 1..cap alpha../. Rats were pretreated with indomethacin to determine if radiation-induced alterations in urine TxB/sup 2/ and 6-keto-PGF/sub 1..cap alpha../ could be suppressed. Pretreatment with indomethacin significantly decreased urine TxB..cap alpha.. and 6-keto-PFG/sub 1..cap alpha../ in both irradiated and nonirradiated animals. Finally, the sources of urinary cyclooxygenase products were investigated using an isogravitometric cross-perfusion system. These experiments demonstrated that urine TxB..cap alpha.. is derived from extrarenal sources, whereas 6-keto-PGF/sub 1..cap alpha.. is synthesized primarily by the kidney. It may be concluded that radiation exposure increases in vivo cyclooxygenase pathway activity by both renal and ultrarenal tissues.

Research Organization:
Georgetown Univ. Medical Center, Washington, DC
OSTI ID:
5751607
Journal Information:
J. Appl. Physiol.: Respir., Environ. Exercise Physiol.; (United States), Journal Name: J. Appl. Physiol.: Respir., Environ. Exercise Physiol.; (United States) Vol. 57:3; ISSN JARPD
Country of Publication:
United States
Language:
English