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Table 2 Therapeutic applications of IGF-1 in neurological diseases

From: Identification of the molecular mechanism of insulin-like growth factor-1 (IGF-1): a promising therapeutic target for neurodegenerative diseases associated with metabolic syndrome

No

Model

Findings

References

1

In vivo/in vitro AD model

In vivo transduction with RAd-IGF1 blocked memory impairment

[206]

2

Brain-specific IGF-1 overexpression mice

IGF-1 treatment reduced depressive and anxiety-like behavior, improved motor coordination, motor learning, visuospatial, and working memory

[207]

3

C57BL/6 J mice/controlled cortical impact/IGF-1

Increased immature neuronal density and neurogenesis of the hippocampus

[208]

4

RIT1−/− mice/IGF-1

IGF-1 facilitates hippocampal neurogenesis through the RIT1/Akt/Sox2 signaling pathway

[39]

5

Old male rats/IGF-1

IGF-1 increases hippocampal neurogenesis and memory accuracy in aged individuals

[209]

6

Old Sprague–Dawley female rats/IGF-1, 18 days ICV

IGF-1 treatment increased the branching of hippocampal astrocytes and reduced their number in the hippocampal striatum radiatum, and improved spatial memory accuracy in aging rats

[210]

7

Female Sprague–Dawley rats/MCAo/IGF-1

IGF-1 reduced infarct volume (39%) and BBB permeability and suppressed IL-6, IL-10, and TNF-α

[211]

8

SH-SY5Y cells/10 nM IGF-1

IGF-1-induced shedding of both APP and APLP1 depends on PI3K, while APLP2 shedding is independent of this signaling pathway

[212]

9

In vitro/PD/IGF-1 along with MPP+

IGF-1 increases cell viability and decreases cell apoptosis

[213]

10

SH-EP1 cell lines/IGF-1 MPP+ neurotoxicity

Inhibition of MPP+-induced apoptosis by activating JNK by PI3K/AKT/GSK3β pathway

[106]

11

PD (WT, A30P and A53 T mutant)/100 ng/mL

Rescue from α-synuclein toxicity and suppression of α-synuclein aggregation

[214]

12

MT-IGF mice

Inhibits β-cell apoptosis, insulin secretion, and hepatic glucose production

[114]

13

Rat/6-OHDA/IGF-1 transgenic neurospheres

Reduction in amphetamine-induced rotation and increased survival of human neural progenitor cells (hNPC) exert trophic effects on degenerate dopamine neurons in the PD model

[103]

14

Adult female Long-Evans rats/6-OHDA/MPTP/IGF-1

By activating PI3K/Akt signaling, IGF-1 improved motor behavior and reduced DA loss in SNc

[105]

15

APP/PS2 mice IGF-1 (50 g/kg dose, i.p.)

Reverses spatial learning and memory impairment and reduces total brain Aβ deposition

[24]

16

Male Wistar rats/6-OHDA/GPE (3 mg/kg, i.p.)

Increased motor movement and reduced dopamine neuronal loss in PD rats

[101]

17

Adult female Long-Evans rats/6-OHDA/MPTP/IGF-1

IGF-1 significantly reduced the loss of asymmetric movement of the forelimb, reduced SNc neuronal loss, and TH immunoreactivity in DA fibers and striatum

[102]

18

Wistar rats/LID mice IGF-1: 50 µg/kg/rat/day

Reduced the brain Aβ burden and upregulated the brain levels of Aβ carriers

[83]

19

In vitro/IGF-1 (0.5 mg/mL)/dopamine

Decrease in apoptosis was accompanied by an increase in Bcl-2 levels

[4]

20

APP (WT-APP and V642I-APP mutant)/IGF-1: 10 nM

IGF-1 protected cells from APP-induced apoptosis and suppressed the cleavage of procaspase-3

[5]

21

Male BN × F344 rats/IGF-1 (50 ng/0.5 μL/h, i.c.v)

IGF-1 administration restored neurogenesis via a three-fold increase in neuronal production

[36]

22

Sprague–Dawley/hx rats/carotid artery IGF-1 infusion; 1.25 mg/kg per day)

IGF-1 increases progenitor cell proliferation and selectively induces neurogenesis in the progeny of adult neural progenitor cells in the hippocampus

[37]

23

Male Wistar rats/6-OHDA/GPE

A single dose of GPE increased TH immunoreactivity and reduced TH immunoreactive neuronal cell death in SNc and striatum

[100]