Evidence map›Paper›PMID 40889011›Full record

ReviewInflammopharmacology2025

Unlocking therapeutic potential in traumatic brain injury: exploring microenvironmental targets, signaling pathways and translational hurdles.

Deepankar Bahuguna, Etikala Amulya, Shristi Arya, Soham Loharkar, Ganesh Vambhurkar, Saptarshee Bhattacharjee, Dinesh Kumar Chandanapalli, Jitender Madan, Saurabh Srivastava

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Post-Translational Modifications in Traumatic Brain Injury: Decoding the Proteomic Landscape and Molecular Mechanisms of Secondary Injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

9 authors.

Deepankar Bahuguna *Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Etikala Amulya *Pharmaceutical Innovation and Translational Research Lab (PITRL), Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana, India.
Shristi AryaDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Soham LoharkarDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Ganesh VambhurkarPharmaceutical Innovation and Translational Research Lab (PITRL), Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana, India.
Saptarshee BhattacharjeeDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Dinesh Kumar ChandanapalliDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
Jitender MadanDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India. jitenderpharmacy@gmail.com.
Saurabh SrivastavaPharmaceutical Innovation and Translational Research Lab (PITRL), Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana, India. saurabh@niperhyd.ac.in.ORCID http://orcid.org/0000-0003-0723-4363

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a catastrophic event resulting from external mechanical forces, leading to a variety of neurological impairments. The complexity and heterogeneity of injuries are among the major speculated reasons for various unmet clinical needs in the effective management of TBI. Brain damage due to TBI results in both primary and secondary injury mechanisms. The complicated molecular pathophysiological alterations of TBI involving oxidative stress, neuroinflammation, excitotoxicity, and apoptosis emphasize the need for a greater understanding of the various signaling pathways that enable the appropriate application of multiple therapeutics for TBI management. This review delves into the multifaceted nature of TBI, involving the pathophysiology and various microenvironmental alterations that occur in TBI. In addition, different signaling pathways implicated in TBI have been elaborated in detail, including their role in TBI progression. The various potential targeting moieties that mitigate the TBI progression have been discussed. The existing clinical status of TBI therapeutics and their translational hurdles, as well as emerging advances in TBI therapy, have been comprehensively addressed.

Indexed as

Brain Injuries, TraumaticSignal TransductionAnimalsHumansOxidative StressBlood–brain barrierMicroenvironmental alterationsNeuroinflammationSignaling pathwayTraumatic brain injury

Identifiers

PMID40889011

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.