Influence of ovarian hormones on cortical spreading depression and its suppression by L-kynurenine in rat

• Published in: PloS one Vol. 8; no. 12; p. e82279
• Main Authors: Chauvel, Virginie, Schoenen, Jean, Multon, Sylvie
• Format: Journal Article Web Resource
• Language: English
• Published: United States Public Library of Science 10.12.2013; Public Library of Science (PLoS)
• Subjects: 17β-Estradiol; Animals; Cerebral Cortex - metabolism; Cerebral Cortex - physiopathology; Cholesterol; Cortex (occipital); Cortical spreading depression; Depression - metabolism; Depression - physiopathology; Estradiol; Estradiol - metabolism; Estradiol - pharmacology; Estrogens; Estrogens - metabolism; Estrogens - pharmacology; Estrous Cycle - drug effects; Estrus cycle; Excitability; Female; Females; Headache; Hormones; Human health sciences; Implantation; Kynuramine - pharmacology; Kynurenic acid; Kynurenine; Migraine; Neurologie; Neurology; Neurosciences & behavior; Neurosciences & comportement; Occipital lobe; Organic acids; ovarian hormones; Ovariectomy; Potassium chloride; Pregnancy; Progesterone; Progesterone - metabolism; Progesterone - pharmacology; Rats; Rats, Sprague-Dawley; Rodents; Sciences de la santé humaine; Sciences sociales & comportementales, psychologie; Sex hormones; Sexual dimorphism; Social & behavioral sciences, psychology; Sodium chloride; Spreading; Womens health
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0082279

Migraine is sexually dimorphic and associated in 20-30% of patients with an aura most likely caused by cortical spreading depression (CSD). We have previously shown that systemic L-kynurenine (L-KYN), the precursor of kynurenic acid, suppresses CSD and that this effect depends on the stage of the estrous cycle in female rats. The objectives here are to determine the influence of ovarian hormones on KCl-induced CSD and its suppression after L-KYN by directly modulating estradiol or progesterone levels in ovariectomized rats. Adult female rats were ovariectomized and subcutaneously implanted with silastic capsules filled with progesterone or 17β-estradiol mixed with cholesterol, with cholesterol only or left empty. Two weeks after the ovariectomy/capsule implantation, the animals received an i.p. injection of L-KYN (300 mg/kg) or NaCl as control. Thirty minutes later CSDs were elicited by applying KCl over the occipital cortex and recorded by DC electrocorticogram for 1 hour. The results show that both estradiol and progesterone increase CSD frequency after ovariectomy. The suppressive effect of L-KYN on CSD frequency, previously reported in normal cycling females, is not found anymore after ovariectomy, but reappears after progesterone replacement therapy. Taken together, these results emphasize the complex role of sex hormones on cortical excitability. The CSD increase by estradiol and, more surprisingly, progesterone may explain why clinically migraine with aura appears or worsens during pregnancy or with combined hormonal treatments.