Premium
Crocetin Inhibits mRNA Expression for Tumor Necrosis Factor‐α, Interleukin‐1β, and Inducible Nitric Oxide Synthase in Hemorrhagic Shock
Author(s) -
Yang Rongjie,
Tan Xiaoyu,
Thomas Ann M.,
Shen Jing,
Qureshi Nilofer,
Morrison David C.,
Van Way Charles W.
Publication year - 2006
Publication title -
journal of parenteral and enteral nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.935
H-Index - 98
eISSN - 1941-2444
pISSN - 0148-6071
DOI - 10.1177/0148607106030004297
Subject(s) - resuscitation , nitric oxide synthase , medicine , anesthesia , shock (circulatory) , crocetin , tumor necrosis factor alpha , mean arterial pressure , nitric oxide , pharmacology , endocrinology , blood pressure , heart rate , crocus sativus , traditional medicine
Background: Inflammatory factors play an important role in cellular damage after shock and resuscitation. Crocetin, a saffron‐derived carotenoid, has been shown to improve postshock recovery of cellular adenosine triphosphate (ATP) and to increase overall survival in an experimental model of hemorrhagic shock. The hypothesis of the present study is that treatment with crocetin at the beginning of resuscitation suppresses subsequent expression of messenger ribonucleic acid (mRNA) for tumor necrosis factor (TNF‐α), interleukin‐1 (IL‐1β) and inducible nitric oxide synthase (iNOS). Methods: Male Sprague‐Dawley rats (n = 45, 350 ± 30 g) were randomly assigned to 5 groups of 9 animals each. After anesthesia with isoflurane, the femoral artery and vein were surgically cannulated. Hemorrhagic shock was induced by withdrawing blood through the arterial cannula until the mean arterial pressure (MAP) was 25–30 mm Hg and maintained at the level for 30 minutes with further withdrawals. Resuscitation was carried out by giving 21 mL/kg Ringer's lactate (LR) and returning the shed blood, with or without the initial administration of crocetin (2 mg/kg). Controls were normal (anesthesia only), sham (surgical preparation), and shock (preparation and shock). Rats were killed 30 minutes after completion of resuscitation. Liver samples were collected for reverse transcription‐polymerase chain reaction (RT‐PCR) analysis of mRNA (TNF‐α, IL‐1β, iNOS, and β‐actin). Results: Liver mRNA expression for TNF‐α, IL‐1β, and iNOS was found in more animals in the shock and shock‐plus‐resuscitation groups than in the sham control group. The group resuscitated from shock with crocetin had mRNA expression for TNF‐α, IL‐1β, and iNOS in fewer animals than either of the other shock groups and was no different from the sham control group. Conclusions: Crocetin modified the hepatic mRNA expression of cytokines and iNOS in a shock model. This agent continues to show promise as a potential treatment for hemorrhagic shock.