Study on nitric oxide and GABA in the hypothalamic paraventricular nucleus and prefrontal cortex under stress
| Project/Area Number |
13671018
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Psychiatric science
|
|---|
| Research Institution | 宮崎医科大学 |
|---|
Principal Investigator |
ISHIZUKA Yuta Miyazaki Medical College, Lecturer, 医学部, 講師 (20264377)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
ISHIDA Yasushi Miyazaki Medical College, Professor, 医学部, 教授 (20212897)
HASHIGUCHI Hiroyuki Miyazaki Medical College, Assistant, 医学部, 助手 (40305090)
|
|---|
| Project Period (FY) |
2001 – 2002
|
| Project Status |
Completed (Fiscal Year 2002)
|
| Budget Amount *help |
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2002: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2001: ¥1,600,000 (Direct Cost: ¥1,600,000)
|
|---|
| Keywords | paraventricular nucleus / medial prefrontal cortex / interleukin-1β / nitric oxide / γ-aminobutyric acid(GABA) / 視床下部質傍核 / 内側前頭野 / 前頭前野 / マイクロダイアリシス |
|---|
| Research Abstract |
We have suggested previously that intraperitoneal (I.p.) administration of interleukin-1β (IL-1β) increases nitric oxide (NO) levels in the hypothalamic paraventricular nucleus (PVN). Using an in vivo brain microdialysis technique, we measured extracellular levels of NO metabolites (Nox^-) in the hypothalamic PVN upon perfusion of selective γ-aminobutyric acid (GABA) receptor antagonist as well as agonist into the medial prefrontal cortex (mPFC) through a microdialysis probe. We examined the effects of selective GABAA receptor antagonist and agonist on IL-1β-induced NO releases in the PVN in conscious rats. Double immunostaining for Fos and neuronal nitric oxide synthase (nNOS) was also used to examine whether nNOS-immunoreactive neurons in the PVN are activated to express Fos immunoreactivity by I.p. injection of IL-Iβ in the rat. The elevated levels of Nox^- in the PVN after I.p. administration IL-1β (4μg/kg) were attenuated by perfusion of muscimol (50 μM), a GABAA receptor agonist, into the mPFC. We also examined the effect of GABAB receptor antagonist and agonist on IL-1β-induced NO releases in the PVN in conscious rats. Perfusion of baclofen (250 μM), a GABAB receptor agonist, into the mPFC had no effect on the elevated levels of Nox^- in the PVN after I.p administration IL-1β(4 μg/kg). Perfusion of saclofen (50 μM), a GABAB receptor antagonist, into the mPFC had no effect on the elevated levels of Nox^- in the PVN after I.p. administration IL-1β(4 μg/kg). Quantitative analysis revealed that some nNOS-positive PVN neurons are activated by IL-1β(4 μg/kg, I.p.) administration. These findings are likely to provide helpful clues to our understanding of the inhibitory modulation of IL-1β-induced NO metabolites releases in the PVN by GABAA and GABAB receptors in the mPFC.
|
Report
(3 results)
Research Products
(13 results)
-
-
-
-
[Publications] Kannan H, Kunitake T, Kato K, Saita M, Shirasaka T, Nose K, Jin Q-H, Ishizuka Y: "Adaptive changes in the sympathetic nervous and endocrine systems during fever induced by interleukin-1β in conscious rats : Potential neural mechanism"Kosaka M, et al.(eds) : Thermotherapy for Neoplasia, Inflammation and Pain Springer-Verlag, Tokyo. 280-289 (2001)
Description
「研究成果報告書概要(和文)」より
Related Report
-
-
-
-
[Publications] Kannan H., Kunitake T., Kato K., Saita M., Shirasaka T., Nose K., Jin Q.-H. & Ishizuka Y., Ed. Kosaka M et al.: "Adaptive changes in the sympathetic nervous and endocrine systems during fever induced by interleukin-1β in conscious rats : Potential neural mechanism., Thermotherapy for Neoplasia, Inflammation, and Pain."Springer-Verlag. 280-289 (2001)
Description
「研究成果報告書概要(欧文)」より
Related Report
-
-
-
-
-
[Publications] Kannan H, Kunitake T, Kato K, Saita M, Shirasaka T, Nose K, Jin Q-H, Ishizuka Y: "Thermotherapy for Neoplasia, Inflammation, and Pain"Springer-Verlag, Tokyo. 280-289 (2001)
