Skip to main content
. 2020 Jun 5;10(6):989. doi: 10.3390/ani10060989

Table 2.

Summary of included studies.

Author Strain Sex Age at Intervention Animals per Group Study Design Intervention Accompanying Conditions Frequency of Intervention (Occasions) Comparator Outcome
Aasland et al. 2010 [22] C57BL/6JBomTac M NR n = 8 RCT (crossover) Saphenous vein
Tail vein
N/A 4 by both methods at 2 weeks apart Each other
Time series
Plasma glucose
Hemolysis
Abatan et al. 2008 [9] ICR F NR n = 8–13 (unclear from methods) RCT Saphenous vein
Tail tip amputation
N/A One-off collection
Serial sample at 2–3 day intervals (4)
Each other
Time series
Plasma corticosterone
Behaviours noted during blood collection
Christensen et al. 2009 [23] C57BL/6JBom M NR n = 20 RCT All sample methods were performed at 21 and 30 °C, i.e., 8 experimental groups
Retrobulbar
Tail incision
Tail tip amputation
Tail tip puncture
N/A Serial sample at 30 min intervals (4) Other groups Blood glucose
Haemolysis
Clotting
Durschlag et al. 1996 [24] ICR M 9 weeks n = 8 Case report Tail incision N/A Serial sample at 2–3 day intervals (5) Time series Histology
Plasma corticosterone
Fernandez et al. 2009 [25] C57BL/6J M 6 weeks n = 10 RCT (crossover) Retrobulbar
Facial vein
Anaesthesia (retrobulbar) Serial sample at 6–8 week intervals (3) Each other Blood glucose
Haemolysis
Forbes et al. 2010 [26] Balb/c F 6–8 weeks n = 214 Retrospective case series Facial vein Lancet or needle for sampling Serial sample at 2–7 day intervals (6) Nil Mortality
Francisco et al. 2015 [27] BALB/c F 5 weeks n = 20 RCT Facial vein
(lancet or needle)
Facial vein
route with anaesthesia as one group
One-off collection Other groups Adverse events
Gross post-mortem site evaluation
Fried et al. 2015 [28] C57BL/6N background with a mutation in MDA5 M/F 4–6 months n = 8 RCT Retrobulbar Anaesthesia One-off collection Time series at 0, 1, 3, 7 or 14 days after sampling Clinical scores
Histology
Frolich et al. 2018 [29] C57BL/6NCrl F 12–14 weeks n = 12 RCT Retrobulbar
Facial vein
Anaesthesia (retrobulbar) One-off collection
Serial sample at 1 wk intervals (6)
Each otherSingle versus serial Adverse events
Mortality
Bodyweight
Histology
Plasma glucose
Gjendal et al. 2020 [30] C57BL/6 F 10 weeks n = 30 RCT Retrobulbar
Facial vein
Sublingual
Anaesthesia (retrobulbar)
Facial vein and sublingual anaesthesia groups, in addition to conscious sampling
Serial sample at days 8, 9, and 10 (short protocol) and days 8, 15, and 22 (long protocol) Eachother
Single versus serial
Nest build score
Faecal corticosteroid metabolites
Bodyweight
Haemolysis
Clotting
Gross post-mortem site evaluation
Harikrishnan et al. 2018 [12] C57BL/6NTac M/F 6 weeks n = 12 RCT Retrobulbar
Sublingual
Facial vein
Tail incision
Anaesthesia (retrobulbar) Serial sample at 24 h interval (2) Other groups, plus isoflurane control, and behavioural test control (naïve animals) Nest build score
Elevated plus maze
Open field test
Faecal corticosteroid metabolites
Heimann et al. 2009 [4] Crl: CD-1 [CR] M/F 11 weeks n = 30 RCT Sublingual
Retrobulbar
Anaesthesia One-off collection Each other Histology
Heimann et al. 2010 [1] CD1 F 14 weeks n = 18 RCT Sublingual
Facial vein
Anaesthesia (for sublingual and one facial vein group) One-off collection Other groups, time series at 3 h, two or five days after sampling Bodyweight
Food intake
Histology
Blood glucose
Kim et al. 2018 [10] CD-1
C57BL/6
M NR n = 4–6 RCT Retrobulbar
Tail tip amputation
Anaesthesia (retrobulbar)
Restrain/unrestrained
One-off collection
Serial sample tail tip groups at 30 min intervals (5)
Other groupsTime series Plasma corticosterone
Madetoja et al. 2009 [31] Hsdwin:NMRI F 9 weeks n = 10 RCT Saphenous vein
Facial vein
Tail vein
Tail warming heat lamp One-off collection Other groups, and control with no blood samples Plasma corticosterone
Plasma ACTH
Moore et al. 2017 [32] C57BL/6J M 10–12 weeks n = 8–12 RCT Facial vein
Tail tip amputation
Tail incision
N/A One-off collection Other groups, and sham submandibular and tail tip amputation (just restraint) Blood glucose
Audible vocalisations
Post-procedural epochs of inactivity
Grooming behaviour
Nest build score
Elevated plus maze
Open field test
Histology
Regan et al. 2016 [33] CD1 F 12–13 weeks n = 15 RCT Retrobulbar
Facial vein
Submental
Anaesthesia (retrobulbar) Serial sample at 2 week intervals (3) Other groups Adverse events
Bodyweight
Extraneous blood loss
Gross post-mortem site evaluation
Haemolysis
Clotting
Rogers et al. 1999 [34] Study 1 (single sample) C57BL/6 F 10–12 weeks n = 72 RCT (crossover) Retrobulbar Thermostatic warming chamber One-off collection (each method) Each other Plasma glucose
Study 2 (repeated sample) C57BL/6 F 10–12 weeks n = 48 Tail incision Serial sample at 1 week interval (2) Plasma insulin
Sadler et al. 2013 [7] Study 1 (single sample) BALB/CAnNCrl
Study 2 (repeated sample) BALB/CAnNCrl
M
M
7–8 weeks
3–4 weeks
n = 5
n = 4/5
RCT Tail incision
Tail vein
Tail incision
Thermostatic warming chamber
Tail dipped hot water
One-off collection
Serial sample at 24 h intervals (3)
Other groups
Time series
Plasma corticosterone
Shirasaki et al. 2012 [35] ICR
C57BL/6N
M 6 weeks n = 10 (unclear from methods) RCT Jugular
Tail incision
N/A One-off collection
Serial sample at 24 h intervals (5)
Each other
Time series
Plasma CRP
Plasma corticosterone
Plasma haemoglobin
Hematocrit
Plasma thrombin–antithrombin complexes
Sorenson et al. 2019 [36] C57BL/6NTac F 8 weeks n = 36 RCT Retrobulbar
Saphenous
Sublingual
Facial vein
Tail incision
Tail tip amputation
Anaesthesia (retrobulbar) One-off collection Each other, plus isoflurane control and naïve animals (no bleeding)
Time series at nine timepoints: 6 or 10 h or 1, 2, 4, 6, 8, 10, or 12 days after sampling
Bodyweight
Stomach contents
Plasma corticosterone
Inflammatory gene expression at sample site
Plasma inflammatory markers (haptoglobin and IL1ß)
Histology
Tabata et al. 1998 [37] Study 1 (single sample) B6C3Fl/ICR
Study 2 (repeated sample) B6C3Fl
M/F
M/F
8 weeks
9 weeks
n = 12
n = 20
RCT Tail tip amputation Tube restraint or anaesthetized with ether or pentobarbital § One-off collection
Serial sample at varied intervals for 24 h (8)
Other groups
Time series
Plasma glucose
Teilmann et al. 2014a [2] BomTac:NMRI M 6–8 weeks n = 8–18 RCT Facial vein
Tail vein
N/A Two day and two night samples within 24 h (4) Other groups, plus controls (no blood sample and naïve animals as behavioural control) Bodyweight
Plasma corticosterone
Faecal corticosteroid metabolites
Triple test (elevated plus maze,
open field test,
light–dark box)
Teilmann et al. 2014 [38] C57BL/6J M 5 months n = 8–12 RCT Retrobulbar
Facial vein
N/A One-off collection Other group, plus control (no blood sample) Bodyweight
Plasma corticosterone
Histology
Tsai et al. 2015 [8] BALB/cO1aHsd F 8 weeks n = 12 RCT Jugular
Retrobulbar (with and without anaesthesia)
Saphenous
Facial vein
Tail vein
Anaesthesia (retrobulbar group and jugular) One-off collection Other groups In-cage activity
Plasma corticosterone
Open field test
Histology
Tuli et al. 1995 [11] Study 1 (acute stress) BALB/c/Ola
Study 2 (tail bleeding recovery) BALB/c/Ola
M
M
5–6 months
5–6 months
n = 5
n = 5
RCT Tail tip amputation Tail dipped hot water One-off collection each route
Serial humane killing at day 2, 4 and 8 after blood sample
Other groups and control with no tail amputation Plasma corticosterone
Adrenal weight
Spleen weight
Voigt et al. 2013 [13] C57BL/6CrlN F 4–6 months n = 36 (16 contributed to final results due to technical failure) RCT (crossover) Blood-sucking bug
Retrobulbar
Tail incision
Anaesthesia (retrobulbar) One-off collection each route (note crossover design) Other groups Faecal corticosteroid metabolites

NR—not reported. §—The aim of this section of the study was to investigate common scenarios, such as anaesthesia, which elevated blood glucose in laboratory mice, rather than investigate the blood sampling technique per se. The reviewers still considered the study was worthy of inclusion since it could provide data on the topic but have only extracted data relevant to the review question. Note: Restraint not included as an accompanying condition unless effects of this specifically investigated as part of study design, since this would be needed for all sample routes.