{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,8]],"date-time":"2026-05-08T20:58:20Z","timestamp":1778273900095,"version":"3.51.4"},"reference-count":19,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Hypertension"],"published-print":{"date-parts":[[1999,1]]},"abstract":"<jats:p><jats:italic>Abstract<\/jats:italic>\u2014Substance P and calcitonin gene\u2013related peptide (CGRP) are colocalized in renal pelvic sensory nerves. Increasing renal pelvic pressure results in an increase in afferent renal nerve activity that is blocked by a substance P receptor antagonist but not by a CGRP receptor antagonist. CGRP potentiates the effects of substance P by preventing the metabolism of substance P. Therefore, we examined whether CGRP enhanced the afferent renal nerve activity responses to substance P and increased renal pelvic pressure, a stimulus known to increase substance P release. Combined administration of substance P and CGRP into the renal pelvis resulted in an increase in afferent renal nerve activity (1392\u00b1217% \u00b7 s; area under the curve of afferent renal nerve activity versus time) that was greater (<jats:italic>P<\/jats:italic>&lt;0.01) than that produced by substance P (620\u00b1156% \u00b7 s) or CGRP (297\u00b196% \u00b7 s) alone. Likewise, CGRP enhanced the afferent renal nerve activity response to increased renal pelvic pressure. During renal pelvic administration of the neutral endopeptidase inhibitor thiorphan, the afferent renal nerve activity response to substance P plus CGRP was similar to that produced by either neuropeptide alone. Because these studies suggested that CGRP potentiated the afferent renal nerve activity responses to substance P, we examined whether the afferent renal nerve activity response to CGRP was blocked by a substance P receptor antagonist, RP67580. RP67580 blocked the afferent renal nerve activity response to CGRP by 85\u00b112% (<jats:italic>P<\/jats:italic>&lt;0.02). We conclude that CGRP activates renal pelvic sensory nerves by retarding the metabolism of substance P, thereby increasing the amount of substance P available for stimulation of substance P receptors.<\/jats:p>","DOI":"10.1161\/01.hyp.33.1.493","type":"journal-article","created":{"date-parts":[[2012,6,12]],"date-time":"2012-06-12T00:53:46Z","timestamp":1339462426000},"page":"493-498","update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":31,"title":["CGRP Activates Renal Pelvic Substance P Receptors by Retarding Substance P Metabolism"],"prefix":"10.1161","volume":"33","author":[{"given":"Jose\u0301 R.","family":"Gontijo","sequence":"first","affiliation":[{"name":"From the Department of Internal Medicine, Department of Veterans Affairs Medical Center, and the University of Iowa College of Medicine (Iowa City)."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lori A.","family":"Smith","sequence":"additional","affiliation":[{"name":"From the Department of Internal Medicine, Department of Veterans Affairs Medical Center, and the University of Iowa College of Medicine (Iowa City)."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ulla C.","family":"Kopp","sequence":"additional","affiliation":[{"name":"From the Department of Internal Medicine, Department of Veterans Affairs Medical Center, and the University of Iowa College of Medicine (Iowa City)."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"e_1_3_2_1_2","first-page":"R2009","volume":"272","year":"1997","unstructured":"Kopp UC, Farley DM, Smith LA. 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