α-Melanocyte-stimulating hormone inhibits renal injury in the absence of neutrophils

H. Chiao, Y. Kohda, P. McLeroy, L. Craig, S. Linas, R. A. Star

Research output: Contribution to journalArticle

53 Citations (Scopus)

Abstract

Background. We previously showed that α-melanocyte stimulating hormone (α-MSH) decreases ischemia/reperfusion injury even when started six hours after ischemia. α-MSH inhibits both neutrophil accumulation and nitric oxide production. To determine the relative importance of α-MSH on the neutrophil pathway, we examined the effects of α-MSH in injury models where neutrophil effects are minimal or absent. Methods. We studied the effects of α-MSH in (1) intercellular adhesion molecule-1 (ICAM-1) knock-out and background mice that were subjected to 40 minutes of ischemia and 24 hours reperfusion, and (2) isolated kidneys that were subjected to in vivo ischemia for 20 minutes and then perfused ex vivo for one hour without neutrophils. To begin to search for direct tubule effects of α-MSH, we studied the effect of α-MSH on nitric oxide (NO) in endotoxin/interferon-γ-treated mouse cortical tubule cells. Results. ICAM-1 knock-out mice had 75% less neutrophil infiltration than background mice after ischemia. Despite the relative lack of neutrophils, α-MSH inhibited renal injury in ICAM-1 knock-out mice. α-MSH also significantly preserved GFR and tubular sodium reabsorption in the isolated perfused ischemic kidney model. α-MSH and a nitric oxide inhibitor did not exhibit synergy. Finally, α-MSH inhibited nitrite production by 20% in the mouse cortical tubule cells (MCT), similar to parallel observations in a cultured mouse macrophage line (RAW cells). Conclusions. We conclude that α-MSH decreases renal injury when neutrophil effects are minimal or absent, indicating that α-MSH inhibits neutrophil-independent pathways of renal injury. The preservation of sodium absorption ex vivo and inhibition of nitrite production in cultured MCT cells suggests that α-MSH inhibits tubular injury by direct tubular effects.

Original languageEnglish (US)
Pages (from-to)765-774
Number of pages10
JournalKidney International
Volume54
Issue number3
StatePublished - 1998

Fingerprint

Melanocyte-Stimulating Hormones
Neutrophils
Kidney
Wounds and Injuries
Intercellular Adhesion Molecule-1
Ischemia
Knockout Mice
Nitric Oxide
Nitrites
Sodium
Neutrophil Infiltration
Reperfusion Injury
Endotoxins

Keywords

  • α-MSH
  • ICAM-1
  • Ischemia
  • Neutrophils
  • Nitric oxide
  • Reperfusion

ASJC Scopus subject areas

  • Nephrology

Cite this

Chiao, H., Kohda, Y., McLeroy, P., Craig, L., Linas, S., & Star, R. A. (1998). α-Melanocyte-stimulating hormone inhibits renal injury in the absence of neutrophils. Kidney International, 54(3), 765-774.

α-Melanocyte-stimulating hormone inhibits renal injury in the absence of neutrophils. / Chiao, H.; Kohda, Y.; McLeroy, P.; Craig, L.; Linas, S.; Star, R. A.

In: Kidney International, Vol. 54, No. 3, 1998, p. 765-774.

Research output: Contribution to journalArticle

Chiao, H, Kohda, Y, McLeroy, P, Craig, L, Linas, S & Star, RA 1998, 'α-Melanocyte-stimulating hormone inhibits renal injury in the absence of neutrophils', Kidney International, vol. 54, no. 3, pp. 765-774.
Chiao, H. ; Kohda, Y. ; McLeroy, P. ; Craig, L. ; Linas, S. ; Star, R. A. / α-Melanocyte-stimulating hormone inhibits renal injury in the absence of neutrophils. In: Kidney International. 1998 ; Vol. 54, No. 3. pp. 765-774.
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abstract = "Background. We previously showed that α-melanocyte stimulating hormone (α-MSH) decreases ischemia/reperfusion injury even when started six hours after ischemia. α-MSH inhibits both neutrophil accumulation and nitric oxide production. To determine the relative importance of α-MSH on the neutrophil pathway, we examined the effects of α-MSH in injury models where neutrophil effects are minimal or absent. Methods. We studied the effects of α-MSH in (1) intercellular adhesion molecule-1 (ICAM-1) knock-out and background mice that were subjected to 40 minutes of ischemia and 24 hours reperfusion, and (2) isolated kidneys that were subjected to in vivo ischemia for 20 minutes and then perfused ex vivo for one hour without neutrophils. To begin to search for direct tubule effects of α-MSH, we studied the effect of α-MSH on nitric oxide (NO) in endotoxin/interferon-γ-treated mouse cortical tubule cells. Results. ICAM-1 knock-out mice had 75{\%} less neutrophil infiltration than background mice after ischemia. Despite the relative lack of neutrophils, α-MSH inhibited renal injury in ICAM-1 knock-out mice. α-MSH also significantly preserved GFR and tubular sodium reabsorption in the isolated perfused ischemic kidney model. α-MSH and a nitric oxide inhibitor did not exhibit synergy. Finally, α-MSH inhibited nitrite production by 20{\%} in the mouse cortical tubule cells (MCT), similar to parallel observations in a cultured mouse macrophage line (RAW cells). Conclusions. We conclude that α-MSH decreases renal injury when neutrophil effects are minimal or absent, indicating that α-MSH inhibits neutrophil-independent pathways of renal injury. The preservation of sodium absorption ex vivo and inhibition of nitrite production in cultured MCT cells suggests that α-MSH inhibits tubular injury by direct tubular effects.",
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AU - Chiao, H.

AU - Kohda, Y.

AU - McLeroy, P.

AU - Craig, L.

AU - Linas, S.

AU - Star, R. A.

PY - 1998

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N2 - Background. We previously showed that α-melanocyte stimulating hormone (α-MSH) decreases ischemia/reperfusion injury even when started six hours after ischemia. α-MSH inhibits both neutrophil accumulation and nitric oxide production. To determine the relative importance of α-MSH on the neutrophil pathway, we examined the effects of α-MSH in injury models where neutrophil effects are minimal or absent. Methods. We studied the effects of α-MSH in (1) intercellular adhesion molecule-1 (ICAM-1) knock-out and background mice that were subjected to 40 minutes of ischemia and 24 hours reperfusion, and (2) isolated kidneys that were subjected to in vivo ischemia for 20 minutes and then perfused ex vivo for one hour without neutrophils. To begin to search for direct tubule effects of α-MSH, we studied the effect of α-MSH on nitric oxide (NO) in endotoxin/interferon-γ-treated mouse cortical tubule cells. Results. ICAM-1 knock-out mice had 75% less neutrophil infiltration than background mice after ischemia. Despite the relative lack of neutrophils, α-MSH inhibited renal injury in ICAM-1 knock-out mice. α-MSH also significantly preserved GFR and tubular sodium reabsorption in the isolated perfused ischemic kidney model. α-MSH and a nitric oxide inhibitor did not exhibit synergy. Finally, α-MSH inhibited nitrite production by 20% in the mouse cortical tubule cells (MCT), similar to parallel observations in a cultured mouse macrophage line (RAW cells). Conclusions. We conclude that α-MSH decreases renal injury when neutrophil effects are minimal or absent, indicating that α-MSH inhibits neutrophil-independent pathways of renal injury. The preservation of sodium absorption ex vivo and inhibition of nitrite production in cultured MCT cells suggests that α-MSH inhibits tubular injury by direct tubular effects.

AB - Background. We previously showed that α-melanocyte stimulating hormone (α-MSH) decreases ischemia/reperfusion injury even when started six hours after ischemia. α-MSH inhibits both neutrophil accumulation and nitric oxide production. To determine the relative importance of α-MSH on the neutrophil pathway, we examined the effects of α-MSH in injury models where neutrophil effects are minimal or absent. Methods. We studied the effects of α-MSH in (1) intercellular adhesion molecule-1 (ICAM-1) knock-out and background mice that were subjected to 40 minutes of ischemia and 24 hours reperfusion, and (2) isolated kidneys that were subjected to in vivo ischemia for 20 minutes and then perfused ex vivo for one hour without neutrophils. To begin to search for direct tubule effects of α-MSH, we studied the effect of α-MSH on nitric oxide (NO) in endotoxin/interferon-γ-treated mouse cortical tubule cells. Results. ICAM-1 knock-out mice had 75% less neutrophil infiltration than background mice after ischemia. Despite the relative lack of neutrophils, α-MSH inhibited renal injury in ICAM-1 knock-out mice. α-MSH also significantly preserved GFR and tubular sodium reabsorption in the isolated perfused ischemic kidney model. α-MSH and a nitric oxide inhibitor did not exhibit synergy. Finally, α-MSH inhibited nitrite production by 20% in the mouse cortical tubule cells (MCT), similar to parallel observations in a cultured mouse macrophage line (RAW cells). Conclusions. We conclude that α-MSH decreases renal injury when neutrophil effects are minimal or absent, indicating that α-MSH inhibits neutrophil-independent pathways of renal injury. The preservation of sodium absorption ex vivo and inhibition of nitrite production in cultured MCT cells suggests that α-MSH inhibits tubular injury by direct tubular effects.

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KW - Neutrophils

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