Evidence map›Paper›PMID 27262314›Full record

ArticleLipids2016

Apricot Kernel Oil Ameliorates Cyclophosphamide-Associated Immunosuppression in Rats.

Honglei Tian, Haiyan Yan, Siwei Tan, Ping Zhan, Xiaoying Mao, Peng Wang, Zhouping Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Lipids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Journal of microbiology and biotechnology · 2026
    Article
  2. Article
  3. Article
  4. Frontiers in pharmacology · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Production, pomological and nutraceutical properties of apricot.Journal of food science and technology · 2019
    Review
  9. Generation of Methicillin-Resistant Staphylococcus Aureus Biofilm Infection in an Immunosuppressed Rat Model.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  10. Effect ofJournal of advanced research · 2017
    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

7 authors at 3 institutions in 2 countries.

Honglei TianFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Haiyan YanFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Siwei TanFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China. 376522415@qq.com.
Ping ZhanFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China. zhanping0993@126.com.
Xiaoying MaoFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Peng WangFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
Zhouping WangFood College of Shihezi University, Shihezi, Xinjiang, People's Republic of China.
657 Oslo · NOShihezi University · CNState Key Laboratory of Food Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effects of dietary apricot kernel oil (AKO), which contains high levels of oleic and linoleic acids and lower levels of α-tocopherol, were evaluated in a rat model of cyclophosphamide-induced immunosuppression. Rats had intraperitoneal injection with cyclophosphamide to induce immunosuppression and were then infused with AKO or normal saline (NS) for 4 weeks. Enzyme-linked immunosorbent assays were used to detect antimicrobial factors in lymphocytes and anti-inflammatory factors in hepatocytes. Hematoxylin & eosin staining was conducted prior to histopathological analysis of the spleen, liver, and thymus. Significant differences were observed between the immune functions of the healthy control group, the normal saline group, and the AKO group. Compared to the normal saline-treated group, lymphocytes isolated from rats administered AKO showed significant improvement in immunoglobulin (Ig)A, IgM, IgG, interleukin (IL)-2, IL-12, and tumor necrosis factor-α (TNF-α) levels (p < 0.01). Liver tissue levels of malondialdehyde and activities of superoxide dismutase and glutathione peroxidase indicated reduced oxidative stress in rats treated with AKO (p < 0.01). Dietary AKO positively affected rat growth and inhibited cyclophosphamide-associated organ degeneration. These results suggested that AKO may enhance the immune system in vivo. These effects may reflect the activities of intermediate oleic and linoleic acid metabolites, which play a vital role in the immune system, and the α-tocopherol in AKO may further enhance this phenomenon. Thus, the use of AKO as a nutritional supplement can be proposed to ameliorate chemotherapy-associated immunosuppression.

Indexed as

AnimalsCyclophosphamideDisease Models, AnimalHepatocytesImmunocompromised HostImmunoglobulinsImmunosuppression TherapyInfusions, ParenteralInjections, IntraperitonealInterleukin-12Interleukin-2LymphocytesMaleOxidative StressPlant OilsPrunus armeniacaCyclophosphamideImmunoglobulinsInterleukin-12Interleukin-2Plant OilsTumor Necrosis Factor-alphaApricot kernel oil (AKO)CyclophosphamideImmune factorImmunosuppressionRat model

Identifiers

PMID27262314
OpenAlexW2410859085

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.