Evidence map›Paper›PMID 27313544›Full record

ArticleFrontiers in physiology2016

Blockade of Rostral Ventrolateral Medulla (RVLM) Bombesin Receptor Type 1 Decreases Blood Pressure and Sympathetic Activity in Anesthetized Spontaneously Hypertensive Rats.

Izabella S Pinto, Aline A Mourão, Elaine F da Silva, Amanda S Camargo, Stefanne M Marques, Karina P Gomes, James O Fajemiroye, Angela A da Silva Reis, Ana C S Rebelo, Marcos L Ferreira-Neto and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Izabella S PintoDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Aline A MourãoDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Elaine F da SilvaDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Amanda S CamargoDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Stefanne M MarquesDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Karina P GomesDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
James O FajemiroyePostgraduate Programme in Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Goiás Goiânia, Brazil.
Angela A da Silva ReisDepartment of Biochemistry and Molecular Biology, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Ana C S RebeloDepartment of Morphology, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Marcos L Ferreira-NetoDepartment of Physiology, College of Physical Education, Federal University of Uberlândia Uberlândia, Brazil.
Daniel A RosaDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
André H Freiria-OliveiraDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Carlos H CastroDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Eduardo ColombariDepartment of Physiology and Pathology, School of Dentistry, São Paulo State University Araraquara, Brazil.
Diego B ColugnatiDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Gustavo R PedrinoDepartment of Physiological Sciences, Center for Neuroscience and Cardiovascular Research, Biological Sciences Institute, Federal University of Goiás Goiânia, Brazil.
Universidade Federal de Goiás · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal de Uberlândia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intrathecal injection of bombesin (BBS) promoted hypertensive and sympathoexcitatory effects in normotensive (NT) rats. However, the involvement of rostral ventrolateral medulla (RVLM) in these responses is still unclear. In the present study, we investigated: (1) the effects of BBS injected bilaterally into RVLM on cardiorespiratory and sympathetic activity in NT and spontaneously hypertensive rats (SHR); (2) the contribution of RVLM BBS type 1 receptors (BB1) to the maintenance of hypertension in SHR. Urethane-anesthetized rats (1.2 g · kg(-1), i.v.) were instrumented to record mean arterial pressure (MAP), diaphragm (DIA) motor, and renal sympathetic nerve activity (RSNA). In NT rats and SHR, BBS (0.3 mM) nanoinjected into RVLM increased MAP (33.9 ± 6.6 and 37.1 ± 4.5 mmHg, respectively; p < 0.05) and RSNA (97.8 ± 12.9 and 84.5 ± 18.1%, respectively; p < 0.05). In SHR, BBS also increased DIA burst amplitude (115.3 ± 22.7%; p < 0.05). BB1 receptors antagonist (BIM-23127; 3 mM) reduced MAP (-19.9 ± 4.4 mmHg; p < 0.05) and RSNA (-17.7 ± 3.8%; p < 0.05) in SHR, but not in NT rats (-2.5 ± 2.8 mmHg; -2.7 ± 5.6%, respectively). These results show that BBS can evoke sympathoexcitatory and pressor responses by activating RVLM BB1 receptors. This pathway might be involved in the maintenance of high levels of arterial blood pressure in SHR.

Indexed as

BB1 receptorsBIM-23127bombesinrostral ventrolateral medullaSHR

Identifiers

PMID27313544
PMCPMC4889888
OpenAlexW2419444083

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.