1. Academic Validation
  2. Cocaine- and amphetamine-regulated transcript peptide produces anxiety-like behavior in rodents

Cocaine- and amphetamine-regulated transcript peptide produces anxiety-like behavior in rodents

  • Eur J Pharmacol. 2003 Mar 7;464(1):49-54. doi: 10.1016/s0014-2999(03)01368-2.
Shigeyuki Chaki 1 Naoya Kawashima Yoshiko Suzuki Toshiharu Shimazaki Shigeru Okuyama
Affiliations

Affiliation

  • 1 Psychiatric Diseases and Pain Research, Medicinal Pharmacology Laboratory, Medicinal Research Laboratories, Taisho Pharmaceutical Co., Ltd., 1-403 Yoshino-cho, Saitama 330-8530, Saitama, Japan. s.chaki@po.rd.taisho.co.jp
Abstract

Cocaine- and amphetamine-regulated transcript (CART) peptide (CART-(55-102)) is involved in the suppression of food intake. We now report that CART-(55-102) is involved in anxiety in rodents. Intracerebroventricularly administered CART-(55-102) as well as intraperitoneal administration of N-methyl-beta-carboline-3-carboxamide (FG-7142), a selective GABA(A)/benzodiazepine receptor inverse agonist, reduced time spent in the open arms in the elevated plus-maze task in mice. CART-(55-102)-induced anxiogenic-like behavior in this task was attenuated by widely prescribed anxiolytics such as diazepam and buspirone. Likewise, CART-(55-102) and FG-7142 significantly reduced social interaction in mice. Both diazepam and buspirone significantly reversed CART-(55-102)-induced anxiogenic-like behavior in social interaction tests. By contrast, another biologically active CART peptide, CART-(62-102), was without effect in the elevated plus-maze task in mice. Moreover, intracerebroventricular administration of CART-(55-102) markedly increased the firing rate of locus coeruleus neurons in single unit recording in anesthetized rats. As CART-(55-102) produced anxiety-like effects in rodents, this peptide may possibly be involved in anxiety and stress-related behavior.

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