Attenuation of angiotensin type 2 receptor function in the rostral ventrolateral medullary pressor area of the spontaneously hypertensive rat
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作者:
Kawabe, Tetsuya
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Rutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USARutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USA
Kawabe, Tetsuya
[1
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Iwasa, Masamitsu
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Rutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USARutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USA
Iwasa, Masamitsu
[1
]
Kawabe, Kazumi
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Rutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USARutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USA
Kawabe, Kazumi
[1
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Sapru, Hreday N.
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Rutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USARutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USA
Sapru, Hreday N.
[1
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机构:
[1] Rutgers New Jersey Med Sch, Dept Neurol Surg, MSB H-586,185 South Orange Ave, Newark, NJ 07103 USA
We hypothesized that blockade of angiotensin II type 2 receptors (AT(2)Rs) in the rostral ventrolateral medullary pressor area (RVLM) may elicit sympathoexcitatory responses which are smaller in hypertensive rats compared to normotensive rats. This hypothesis was tested in urethane-anesthetized, artificially ventilated male 14-week-old spontaneously hypertensive rats (SHR). Age-matched male Wistar-Kyoto rats (WKY) and Wistar rats were used as controls. PD123319 (AT(2)R antagonist) was microinjected into the RVLM and mean arterial pressure (MAP), heart rate (HR) and greater splanchnic nerve activity (GSNA) were recorded. Increases in MAP, HR and GSNA elicited by unilateral microinjections of PD123319 into the RVLM were significantly smaller in SHR when compared with those in WKY and Wistar rats. Unilateral microinjections of l-glutamate (l-Glu) into the RVLM elicited greater increases in MAP and GSNA in SHR compared to those in WKY. AT(2)R immunoreactivity was demonstrated in the RVLM neurons which were retrogradely labeled from the intermediolateral cell column (IML) of the spinal cord. These results indicate that AT(2)Rs are present on the RVLM neurons projecting to the IML and their blockade results in sympathoexcitatory responses. Activation of AT(2)Rs has an inhibitory influence in the RVLM and these receptors are tonically active. Attenuation of the function of AT(2)Rs in the RVLM may play a role in genesis and/or maintenance of hypertension in SHR.
机构:
Mississippi Coll, Clinton, MS 39058 USA
Univ Mississippi, Sch Pharm, Dept Pharmacol, Oxford, MS 38677 USAMississippi Coll, Clinton, MS 39058 USA
Bourassa, Erick A.
Stedenfeld, Kristen A.
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Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA 15260 USAMississippi Coll, Clinton, MS 39058 USA
Stedenfeld, Kristen A.
Sved, Alan F.
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Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA 15260 USAMississippi Coll, Clinton, MS 39058 USA
Sved, Alan F.
Speth, Robert C.
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Univ Mississippi, Sch Pharm, Dept Pharmacol, Oxford, MS 38677 USA
Nova SE Univ, Coll Pharm, Ft Lauderdale, FL 33328 USAMississippi Coll, Clinton, MS 39058 USA
机构:
Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Goto, M
Mukoyama, M
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Mukoyama, M
Sugawara, A
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Sugawara, A
Suganami, T
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Suganami, T
Kasahara, M
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Kasahara, M
Yahata, K
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Yahata, K
Makino, H
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Makino, H
Suga, S
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Suga, S
Tanaka, I
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan
Tanaka, I
Nakao, K
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Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, JapanKyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 6068507, Japan