Evidence map›Paper›PMID 38243941›Full record

ArticleCurrent protein & peptide science2024

Neurokinin B Administration Induces Dose Dependent Proliferation of Seminal Vesicles in Adult Rats.

Muhammad Haris Ramzan, Mohsin Shah, Faiqah Ramzan

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Article in Current protein & peptide science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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

3 authors at 2 institutions in 1 country.

Muhammad Haris RamzanDepartment of Physiology, Khyber Medical University Institute of Medical Sciences (KMU-IMS), Kohat 26000, Pakistan.ORCID 0000-0003-4702-3122
Mohsin ShahDepartment of Physiology, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, 25100, Pakistan.ORCID 0000-0001-9017-9152
Faiqah RamzanDepartment of Animal Sciences, Faculty of Veterinary and Animal Sciences (FVAS), Gomal University, Dera Ismail Khan, 29050, Pakistan.ORCID 0000-0001-9489-7557
Khyber Medical University · PKGomal University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurokinin B; an endogenous decapeptide, mediates its reproductive physiological actions through gonadotropin releasing hormone. Despite the potential role of Neurokinin B on seminal vesicles, its effects on seminal vesicles in adult male mammals remain elusive. We aimed to investigate the potentials of variable doses of Neurokinin B, its agonist and antagonist on histomorphology and expression of NK3R on seminal vesicles, and secretory activity of seminal vesicles in adult male rats.

methodsAdult male Sprague Dawley rats (n=10 in each group) were administered intraperitoneally with Neurokinin B in three variable doses: 1 μg, 1 ηg and 10 ρg while, Senktide (Neurokinin B agonist) and SB222200 (Neurokinin B antagonist) in 1 μg doses consecutively for 12 days. After 12 days of peptide treatment, half of the animals (n=05) in each group were sacrificed while remaining half (n=05) were kept for another 12 days without any treatment to investigate treatment reversal. Seminal vesicles were dissected and excised tissue was processed for light microscopy, immunohistochemistry and estimation of seminal fructose levels.

resultsTreatment with Neurokinin B and Senktide significantly increased while SB222200 slightly decrease the seminal vesicles weight, epithelial height and seminal fructose levels as compared to control. Light microscopy revealed increased epithelial height and epithelial folding as compared to control in all Neurokinin B and Senktide treated groups while decreased in SB222200. Effects of various doses of Neurokinin B, Senktide and SB222200 on seminal vesicles weight, epithelial height, seminal fructose levels and histomorphology were reversed when rats were maintained without treatments. Immuno-expression of Neurokinin B shows no change in treatment and reversal groups.

conclusionContinuous administration of Neurokinin B and Senktide effect positively while SB222200 have detrimental effects on cellular morphology, epithelial height and seminal fructose levels in seminal vesicles. Effects of peptide treatments depicted a reversal towards control group when rats were kept without any treatment.

Indexed as

Neurokinin BPeptide FragmentsRats, Sprague-DawleyReceptors, Neurokinin-3Seminal VesiclesSubstance PAnimalsCell ProliferationDose-Response Relationship, DrugMaleRatsNeurokinin BPeptide FragmentsReceptors, Neurokinin-3Substance Pfructosehistomorphologyimmunohistochemistry.neurokinin BSB222200seminal vesiclessenktidetachykinin receptorsTachykinins

Identifiers

PMID38243941
OpenAlexW4391067970

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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.