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10.46243/jst.2022.v7.i01.pp1-18 registered

Phytochemical and Pharmacological Evaluation of Ethanolic Extract of Moringa Oleifera as Neuroprotective Agent in Vincristine Induced Peripheral Neuropathy

Resolves to https://www.jst.org.in/index.php/pub/article/view/583

Held by Longman Publishers (India) · prefix 10.46243 live · DOI address https://doi.org/10.46243/jst.2022.v7.i01.pp1-18

Registered 29 Sep 2026 via crossref · record version 2 · last change 29 Sep 2026, 11:59 PM · record sha256 2baef2a88333e917…

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JournalArticle — an article in a journal · Digital · Visual · en

Phytochemical and Pharmacological Evaluation of Ethanolic Extract of Moringa Oleifera as Neuroprotective Agent in Vincristine Induced Peripheral Neuropathy (PrincipalTitle)

Published 2022-05-22

Part of Journal of Science & Technology · ISSN 2456-5660 · volume 7 · issue Special 1 · pages 1–18

Agents

  • DHAFER SHAHER MOHAMMED NOMAN (author)
  • Longman Publishers (publisher)

Identifiers DOI 10.46243/jst.2022.v7.i01.pp1-18

Abstract

The objective of this study was to phytochemically analyze the ethanolic extracts of the leaves of Moringa oleifera and thereafter to evaluate its neuroprotective activity in vincristine induced peripheral neuropathy.The fresh leaves of Moringa oleifera were collected, powdered and extracted with ethanol. Thereafter the dried ethanolic extract was subjected to phytochemical analysis using various analytical techniques primarily GC-MS to identify the bioactive phytochemical components. Acute toxicity studies were also carried out on the extract. After overnight fasting peripheral neuropathy was induced in Wistar rats by intraperitoneal injection of vincristine 100μg/kg/day body weight dissolved in saline (0.1ml/kg/day). Group A served as normal control while group B was considered as neuropathy control. Group C was standard receiving methylcobalamin (50μg/kg i. p) and Group D & E neuropathy animals were treated with the extract, dose of 250 and 500 mg/kg/b. w p.o. respectively. During the investigations, studies were carried out by in-vivo models such as tail flick, acetone spray method, pain sensation test, nerve conduction test as well as proinflammatory and antioxidant studies. At the end of study, animals in all groups were sacrificed, the sciatic nerve was dissected and histopathology was performed. The interpretation of the results was done after subjecting the data obtained from various studies to statistical analysis which included descriptive statistics, ANOVA followed by Tukey’s test. Ethanolic extract of Moringa oleifera leaves were phytochemically analyzed and showed presence of bioactive chemicals. The ethanolic extracts produced significant neuroprotective activity it was effective in anti-nociceptive activity, and caused changes in in-vivo anti-oxidants enzyme and nerve conduction. Further significant improvements were noted in pro-inflammatory markers. Histopathology studies indicated amelioration of histological features. In conclusion, the ethanolic extracts of Moringa oleifera leaves showed potential neuroprotective activity against vincristine induced peripheral neuropathy

Licence https://creativecommons.org/licenses/by/4.0/

System metadata — ISO 26324:2025, Annex B · DOI Handbook 10.1

Each element by the standard's name (Annex B: reference elements, then administrative) and the Handbook's (in grey), read off the record above.

ElementValueIn the record
DOI Name
DOI name
10.46243/jst.2022.v7.i01.pp1-18doi
Referent Type
referentType
Creationreferent
Referent Sub-Type
referentSubType
JournalArticle — an article in a journaltype
Referent Name(s)
referentName(s)
Phytochemical and Pharmacological Evaluation of Ethanolic Extract of Moringa Oleifera as Neuroprotective Agent in Vincristine Induced Peripheral Neuropathy (PrincipalTitle, en)titles
Basic Metadata
basicMetadata
author: DHAFER SHAHER MOHAMMED NOMAN
publisher: Longman Publishers
published: 2022-05-22
part of: Journal of Science & Technology · ISSN 2456-5660 · vol. 7 · no. Special 1 · pp. 1–18
language: en
form: Digital · Visual · Language
agents, dates, container, language, structural_type, modes, characters
Referent Identifier(s)
alternateIdentifier(s)
none besides the DOIidentifiers, relations (IsSameAs)
Registration Authority
registrationAuthorityCode
Crossref — issued by Crossref (member 25296); held here as a copyrecord.source_agency (our code, ra_doi_name, for names issued here once appointed)
Created Date
issueDate
2024-02-16record.registered (when the DOI name was first registered)
relatedIdentifiersnone needed — the descriptive metadata is in this recordcontainer, relations (only where the descriptive metadata lives at another identifier)

complete Every System Metadata element is here, with the basic metadata a journal article needs.

The System Metadata Declaration (JSON) · the Kernel Metadata Declaration (XML) · what each sub-type needs

History — the ledger

Every change to this DOI, in order, as it was recorded. Entries are only ever added, never changed or removed.

#WhenWhatByChanges
129 Sep 2026, 10:00 PMregister
registered at Crossref; record read from api.crossref.org
Administrator (admin) 320 fields set · sha256 cfe5e82e6af8…
229 Sep 2026, 11:59 PMupdate
record re-read from api.crossref.org
Administrator (admin)
abstract.value: The objective of this study was to phytochemically analyze the ethanolic extracts of the leaves of Moringa oleifera and thereafter to evaluate its neuroprotective activity in vincristine induced peripheral neuropathy.The fresh leaves of Moringa oleifera were collected, powdered and extracted with ethanol. Thereafter the dried ethanolic extract was subjected to phytochemical analysis using various analytical techniques primarily GC-MS to identify the bioactive phytochemical components. Acute toxicity studies were also carried out on the extract. After overnight fasting peripheral neuropathy was induced in Wistar rats by intraperitoneal injection of vincristine 100μg/kg/day body weight dissolved in saline (0.1ml/kg/day). Group A served as normal control while group B was considered as neuropathy control. Group C was standard receiving methylcobalamin (50μg/kg i. p) and Group D & E neuropathy animals were treated with the extract, dose of 250 and 500 mg/kg/b. w p.o. respectively. During the investigations, studies were carried out by in-vivo models such as tail flick, acetone spray method, pain sensation test, nerve conduction test as well as proinflammatory and antioxidant studies. At the end of study, animals in all groups were sacrificed, the sciatic nerve was dissected and histopathology was performed. The interpretation of the results was done after subjecting the data obtained from various studies to statistical analysis which included descriptive statistics, ANOVA followed by Tukey’s test. Ethanolic extract of Moringa oleifera leaves were phytochemically analyzed and showed presence of bioactive chemicals. The ethanolic extracts produced significant neuroprotective activity it was effective in anti-nociceptive activity, and caused changes in in-vivo anti-oxidants enzyme and nerve conduction. Further significant improvements were noted in pro-inflammatory markers. Histopathology studies indicated amelioration of histological features. In conclusion, the ethanolic extracts of Moringa oleifera leaves showed potential neuroprotective activity against vincristine induced peripheral neuropathy → The objective of this study was to phytochemically analyze the ethanolic extracts of the leaves of Moringa oleifera and thereafter to evaluate its neuroprotective activity in vincristine induced peripheral neuropathy.The fresh leaves of Moringa oleifera were collected, powdered and extracted with ethanol. Thereafter the dried ethanolic extract was subjected to phytochemical analysis using various analytical techniques primarily GC-MS to identify the bioactive phytochemical components. Acute toxicity studies were also carried out on the extract. After overnight fasting peripheral neuropathy was induced in Wistar rats by intraperitoneal injection of vincristine 100μg/kg/day body weight dissolved in saline (0.1ml/kg/day). Group A served as normal control while group B was considered as neuropathy control. Group C was standard receiving methylcobalamin (50μg/kg i. p) and Group D & E neuropathy animals were treated with the extract, dose of 250 and 500 mg/kg/b. w p.o. respectively. During the investigations, studies were carried out by in-vivo models such as tail flick, acetone spray method, pain sensation test, nerve conduction test as well as proinflammatory and antioxidant studies. At the end of study, animals in all groups were sacrificed, the sciatic nerve was dissected and histopathology was performed. The interpretation of the results was done after subjecting the data obtained from various studies to statistical analysis which included descriptive statistics, ANOVA followed by Tukey’s test. Ethanolic extract of Moringa oleifera leaves were phytochemically analyzed and showed presence of bioactive chemicals. The ethanolic extracts produced significant neuroprotective activity it was effective in anti-nociceptive activity, and caused changes in in-vivo anti-oxidants enzyme and nerve conduction. Further significant improvements were noted in pro-inflammatory markers. Histopathology studies indicated amelioration of histological features. In conclusion, the ethanolic extracts of Moringa oleifera leaves showed potential neuroprotective activity against vincristine induced peripheral neuropathy
container.titles.0.value: Journal of Science & Technology → Journal of Science & Technology

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