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Experimental Autoimmune Encephalomyelitis Potentiates Mouse Mast Cell Protease 4-Dependent Pressor Responses to Centrally or Systemically Administered Big Endothelin-1

Desbiens, Louisane (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
Lapointe, Catherine (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
Gendron, Louis (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
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Gharagozloo, Marjan (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
Vincent, Laurence (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
Pejler, Gunnar (author)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Swedish Univ Agr Sci, Dept Anat Physiol & Biochem, Uppsala, Sweden,Institutionen för anatomi, fysiologi och biokemi,Department of Anatomy, Physiology and Biochemistry (AFB),Uppsala University
Gris, Denis (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
D'Orleans-Juste, Pedro (author)
Univ Sherbrooke, Med Sch, Dept Pharmacol & Physiol, Sherbrooke, PQ, Canada
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 (creator_code:org_t)
 
2019-06-27
2019
English.
In: Journal of Pharmacology and Experimental Therapeutics. - : American Society for Pharmacology & Experimental Therapeutics (ASPET). - 0022-3565 .- 1521-0103. ; 370:3, s. 437-446
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Multiple sclerosis is a neurodegenerative disease affecting predominantly female patients between 20 and 45 years of age. We previously reported the significant contribution of mouse mast cell protease 4 (mMCP-4) in the synthesis of endothelin-1 (ET-1) in healthy mice and in a murine model of experimental autoimmune encephalomyelitis (EAE). In the current study, the cardiovascular effects of ET-1 and big endothelin-1 (big-ET-1) administered systemically or intrathecally were assessed in the early preclinical phase of EAE in telemetry instrumented/conscious mice. Chymase-specific enzymatic activity was also measured in the lung, brain, and mast cell extracts in vitro. Finally, the impact of EAE immunization was studied on the pulmonary and brain mRNA expression of different genes of the endothelin pathway, interleukin-33 (IL-33), and monitoring of immunoreactive tumor necrosis factor-α (TNF-α). Systemically or intrathecally administered big-ET-1 triggered increases in blood pressure in conscious mice. One week post-EAE, the pressor responses to big-ET-1 were potentiated in wild-type (WT) mice but not in mMCP-4 knockout (KO) mice. EAE triggered mMCP-4–specific activity in cerebral homogenates and peritoneal mast cells. Enhanced pulmonary, but not cerebral preproendothelin-1 and IL-33 mRNA were found in KO mice and further increased 1 week post-EAE immunization, but not in WT animals. Finally, TNF-α levels were also increased in serum from mMCP-4 KO mice, but not WT, 1 week post-EAE. Our study suggests that mMCP-4 activity is enhanced both centrally and systemically in a mouse model of EAE.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

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