Evidence map›Paper›PMID 32206420›Full record

ArticleBiomedical optics express2020

Fluorescence of serotonin in the visible spectrum upon multiphotonic photoconversion.

Guillermo A Hernández-Mendoza, Dilia Aguirre-Olivas, Mario González-Gutiérrez, Héctor J Leal, Naser Qureshi, Carlos G Treviño-Palacios, Jorge Peón, Francisco F De-Miguel

Abstract read
In one paragraph

Article in Biomedical optics express, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

8 authors.

Guillermo A Hernández-MendozaInstituto de Fisiología Celular-Neurociencias, Universidad Nacional Autónoma de México. Circuito Exterior, Ciudad Universitaria, 04510, D. F., Mexico.
Dilia Aguirre-OlivasInstituto de Fisiología Celular-Neurociencias, Universidad Nacional Autónoma de México. Circuito Exterior, Ciudad Universitaria, 04510, D. F., Mexico.ORCID https://orcid.org/0000-0002-1276-7183
Mario González-GutiérrezInstituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Ciudad de Mexico, 04510, Mexico.
Héctor J LealFacultad de Ingeniería, Universidad Nacional Autónoma de México, Av. Universidad 3000, Ciudad Universitaria, Ciudad de Mexico, 04510, Mexico.
Naser QureshiInstituto de Ciencias Aplicadas y Tecnología, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Ciudad de Mexico, 04510, Mexico.
Carlos G Treviño-PalaciosInstituto Nacional de Astrofísica, Óptica y Electrónica, Luis Enrique Erro #1, 72840 Tonantzintla, Puebla, Mexico.ORCID https://orcid.org/0000-0001-6632-0312
Jorge PeónInstituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Ciudad de Mexico, 04510, Mexico.
Francisco F De-MiguelInstituto de Fisiología Celular-Neurociencias, Universidad Nacional Autónoma de México. Circuito Exterior, Ciudad Universitaria, 04510, D. F., Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vital molecule serotonin modulates the functioning of the nervous system. The chemical characteristics of serotonin provide multiple advantages for its study in living or fixed tissue. Serotonin has the capacity to emit fluorescence directly and indirectly through chemical intermediates in response to mono- and multiphoton excitation. However, the fluorescent emissions are multifactorial and their dependence on the concentration, excitation wavelength and laser intensity still need a comprehensive study. Here we studied the fluorescence of serotonin excited multiphotonically with near-infrared light. Experiments were conducted in a custom-made multiphoton microscope coupled to a monochromator and a photomultiplier that collected the emissions. We show that the responses of serotonin to multiphoton stimulation are highly non-linear. The well-known violet emission having a 340 nm peak was accompanied by two other emissions in the visible spectrum. The best excitor wavelength to produce both emissions was 700 nm. A green emission with a ∼ 500 nm peak was similar to a previously described fluorescence in response to longer excitation wavelengths. A new blue emission with a ∼ 405 nm peak was originated from the photoconversion of serotonin to a relatively stable product. Such a reaction could be reproduced by irradiation of serotonin with high laser power for 30 minutes. The absorbance of the new compound expanded from ∼ 315 to ∼ 360 nm. Excitation of the irradiated solution monophotonically with 350 nm or biphotonically with 700 nm similarly generated the 405 nm blue emission. Our data are presented quantitatively through the design of a single geometric chart that combines the intensity of each emission in response to the serotonin concentration, excitation wavelengths and laser intensity. The autofluorescence of serotonin in addition to the formation of the two compounds emitting in the visible spectrum provides diverse possibilities for the quantitative study of the dynamics of serotonin in living tissue.

Identifiers

PMID32206420
PMCPMC7075609

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.