Evidence map›Paper›PMID 35672152›Full record

ArticlePharmaceutical biology2022

Camel milk protein hydrosylate alleviates hepatic steatosis and hypertension in high fructose-fed rats.

Mohammad A Alshuniaber, Ghedeir M Alshammari, Samy M Eleawa, Abu ElGasim A Yagoub, Abdullrahman S Al-Khalifah, Maha H Alhussain, Laila Naif Al-Harbi, Mohammed Abdo Yahya

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2022. 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
1.5field-weighted citation impact, top 16% 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, 13 citations in OpenAlex.

  1. Review
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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

8 authors at 2 institutions in 2 countries.

Mohammad A AlshuniaberDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Ghedeir M AlshammariDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-2043-1209
Samy M EleawaCollege of Health Sciences, Applied Medical Sciences Department, PAAET, Safat, Kuwait.
Abu ElGasim A YagoubDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Abdullrahman S Al-KhalifahDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Maha H AlhussainDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Laila Naif Al-HarbiDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0003-0778-922X
Mohammed Abdo YahyaDepartment of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-5665-9600
King Saud University · SAPublic Authority for Applied Education and Training · KW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextCamel milk is used in traditional medicine to treat diabetes mellitus hypertension and other metabolic disorders.

objectiveThis study evaluated the antisteatotic and antihypertensive effects of camel milk protein hydrolysate (CMH) in high fructose (HF)-fed rats and compared it with the effects afforded by the intact camel milk protein extract (ICM). MATERIALS AND

methodsAdult male Wistar rats were divided into 6 groups (

resultsBoth ICM and CMH reduced fasting glucose and insulin levels, serum and hepatic levels of cholesterol and triglycerides, and serum levels of ALT and AST, angiotensin II, ACE, endothelin-1, and uric acid in HF-fed rats. In addition, both ICM and CMH reduced hepatic fat deposition in the hepatocytes and reduced hepatocyte damage. This was associated with an increase in the hepatic activity of AMPK, higher PPARα mRNA, reduced expression of fructokinase C, SREBP1, SREBP2, fatty acid synthase, and HMG-CoA-reductase. Both treatments lowered systolic and diastolic blood pressure. However, the effects of CMH on all these parameters were greater as compared to ICM. DISCUSSION AND

conclusionsThe findings of this study encourage the use of CMH in a large-scale population and clinical studies to treat metabolic steatosis and hypertension.

Indexed as

Fatty LiverHypertensionAnimalsCamelusFructoseLiverMaleMilk ProteinsRatsRats, WistarTriglyceridesFructoseMilk ProteinsTriglyceridesangiotensinblood pressurehyperglycaemiahyperlipidaemialiverMetabolic disorderNAFLD

Identifiers

PMID35672152
PMCPMC9176680
OpenAlexW4281701168

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LicenceCC BY-NC
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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.