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Research Note
Revised

The neuro-toxin MPTP does not prevent reproduction in marmosets

[version 2; peer review: 2 approved]
PUBLISHED 22 May 2019
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Abstract

1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is a neuro-toxin that has been employed to model Parkinson’s disease in non-human primates for over 3 decades. Despite its use for such a long period, little is known about the effects of MPTP on reproductive function. Here, we report the case of a male marmoset which was able to procreate 1.5 year after having been administered the toxin. We also report on 1 male and 1 female MPTP-lesioned marmosets which produced babies after being housed together for 5 years. These cases suggest that MPTP may not interfere with marmoset reproductive function or that if it does, it may be for a limited period of time.

Keywords

MPTP, marmoset, reproduction

Revised Amendments from Version 1

In this revised version of the manuscript, we have incorporated the changes suggested by the reviewers. Specifically, we acknowledge that the observations made in the marmoset may not be generalisable to Old World monkeys and we also emphasise the fact that MPTP was administered acutely.

See the authors' detailed response to the review by Joachim Wistuba
See the authors' detailed response to the review by Cécile Moro

Introduction

The common marmoset (Callithrix jacchus) has been used to model Parkinson’s disease since 19841 and since then, nearly 100 experimental drugs that aim at alleviating disease manifestations and treatment-related complications have been assessed in this small primate2. Marmosets are typically rendered parkinsonian by administration of a neuro-toxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which destroys dopaminergic neurons3, leading to a parkinsonian phenotype.

Despite this abundant literature, whether MPTP interferes with marmosets’ ability to procreate has, to our knowledge, not been documented. Here, we report the case of 3 marmosets which were able to generate offspring after having been administered MPTP.

Methods

Animals

Two male and 1 female common marmosets (from McGill University breeding colony), weighing 350–400g, were pair-housed under conditions of controlled temperature (24±1°C), humidity (50%) and a 12h light/dark cycle (07:15 lights on). They were cared for in accordance with a protocol approved by McGill University and the Montreal Neurological Institute Animal Care Committees in accordance with the regulations defined by the Canadian Council on Animal Care. They had unlimited access to water and were fed with marmoset food (Mazuri® Marmoset Jelly, catalogue number 0007066, USA), nuts and fresh fruits twice daily. Home cages were enriched with primate toys, nestboxes and perches. All efforts were made to avoid causing harm to animals; we achieved this by working in close collaboration with the Animal Care Committees and veterinary teams.

Induction and assessment of parkinsonism

Parkinsonism was induced by s.c. injections of MPTP hydrochloride in the back of the animals (2 mg/kg every other day, for 5 days, at 08:30; catalogue number M0896, MilliporeSigma, Canada), as previously reported49. Animals were not sedated during the injections.

Following a 6-week recovery period, a stable parkinsonian phenotype was observed. For behavioural assessment, each marmoset was placed individually into an observation cage (36 × 33 × 22 in) containing food, water and a wooden perch, and left undisturbed for 6 h. Behaviour was recorded via webcam and analysed post hoc by a movement disorder neurologist blinded to the treatment given.

Parkinsonism was scored for 5 min every 10 min using a scale that combined measures of range of movement, bradykinesia, posture, and attention/alertness47,10,11. Range of movement was rated on a 0 to 9 scale: 0 = running, jumping between roof, walls, perch, using limbs through a wide range of activity; 9 = no movement. Bradykinesia was rated from 0 to 3: 0 = normal initiation and speed of movement; 3 = prolonged freezing, akinesia, inability to move. Postural abnormalities were rated 0 or 1: 0 = normal balance, upright posture, head held up; 1 = impaired balance, crouched posture, head down. Attention/alertness was rated 0 or 1; 0 = normal head checking movements, movement of neck in variable directions, smooth, small movements; 1 = reduced or absent head checking, head in one position for more than 50% of observation period. The score attributed to each of the behaviours assessed was the most prevalent of the 5 min observation period. The global parkinsonian was calculated as a combination of the above behaviours according to the following formula: (range of movement × 1) + (bradykinesia × 3) + (posture × 9) + (attention/alertness × 9). The maximal parkinsonian disability score per 5 min observation period was 36.

Housing and breeding

As mentioned above, marmosets were pair-housed. One male marmoset was paired with a female marmoset which had not been exposed to MPTP, while 1 MPTP-lesioned male and 1 MPTP-lesioned female marmosets were housed together.

Behavioural assessment of the young marmosets

To minimise stress to families and to avoid interfering with the rearing process, newborn marmosets were not caught and all observations were made by experienced animal care technicians in the animal’s home cages.

Euthanasia

As we will report later, two newborn marmosets had to be euthanised. They were administered ketamine (Vetoquinol N.-A Inc, Canada) 20 mg/kg intra-muscularly, followed by 100 mg/kg sodium pentobarbital (Vetoquinol N.-A Inc, Canada) intravenously, according to McGill University standard operating procedures (https://www.mcgill.ca/research/research/compliance/animals/animal-research-practices/sop).

Results

Parkinsonism

Acute administration of MPTP resulted in the development of a parkinsonian phenotype, characterised by bradykinesia, hunched posture, reduced activity and reduced alertness in all 3 animals, as previously reported47.

Pairing and breeding

Parkinsonian male marmoset paired with non-parkinsonian female marmoset. At the time of the pairing (May 2017), the male marmoset was 3.5 years old and he was paired with a 3-year old female marmoset. The female marmoset was pregnant at the time of the pairing and gave birth to twin babies (1 male and 1 female baby) 4 months later (September 2017). Despite not being the biological father of these 2 babies, the male marmoset was an active and attentive participant in the rearing of these two babies.

Five months later (February 2018), i.e. 9 months after the pairing, triplets were born, of which 2 survived. Based on our experience, when female marmosets give birth to triplets, it is expected that one baby may not survive, and it is therefore unlikely that this casualty can be attributed to MPTP. Another 6 months later (August 2018), a second set of triplets, of which 2 survived, were born. More recently, twins were born (January 2019).

Thus, the male marmoset that was administered MPTP has so far fathered 8 babies, 6 of which have survived, are healthy and are developing normally, e.g. weaning, range of motion, body size, etc. In addition, the male marmoset has also been actively involved in the care and rearing of the babies.

Parkinsonian male marmoset paired with parkinsonian female marmoset. A male and a female marmoset, both aged ≈ 8 years old, were administered MPTP 5 years ago and have been pair-housed together since then. The female marmoset has been administered monthly injections of progesterone-based contraceptive. Quite unexpectedly, despite the parkinsonian state of both animals and the monthly injections, the female marmoset gave birth to twins in September 2018. Because experiments in which the female marmoset was administered investigational products were conducted during the pregnancy and that the impact of these substances on babies was uncertain, and also because the adequacy of the care provided by the 2 parkinsonian parents was uncertain, a decision was made to euthanise the newly-born marmosets shortly after their birth.

Discussion

Here, we report that marmosets were able to procreate after having been administered with the neuro-toxin MPTP. These cases suggest that MPTP, when administered acutely may not be toxic to the reproductive system, in the marmoset. Moreover, MPTP-exposed marmosets appear to be able to care for their offspring, despite their parkinsonism. It is noteworthy that marmosets are New World monkeys; it is currently unknown whether Old World monkeys, apes or humans would be able to procreate after exposure to MPTP.

In the case of the parkinsonian male marmoset paired with the non-parkinsonian female marmoset, that babies were born 9 months after the pairing occurred makes a strong case that the MPTP-exposed animal is the biological father of the offspring. The average gestation period of a female marmoset lasts 143-144 days, and twin babies are common12; the birth of another set of triplets 5 months after the last delivery is an agreement with the duration and the outcome of a normal pregnancy, as is the subsequent birth of twins.

In the case of the paired MPTP-lesioned marmosets, that the 2 animals were housed exclusively together for years indicates that babies were conceived by 2 parkinsonian animals. It is nevertheless surprising that the female marmoset was able to become pregnant despite the monthly administration of contraceptive. It is possible that the injection was not optimally timed within her cycle; whether MPTP slightly interfered with the cycle duration remains uncertain.

In the brain, MPTP is converted to its toxic metabolite, 1-methyl-4-phenylpyridinium [MPP+] by the enzyme monoamine oxidase B [MAO-B]13 in astrocytes14,15 and then enters dopaminergic neurons via the dopamine transporter16. The dopamine transporter is expressed, albeit at low levels, in the hypothalamus17,18, and MPTP administration was shown to produce degenerative changes to hypothalamic dopaminergic neurons, in the marmoset19. This could, in theory, lead to disruption of the hypothalamo – hypophyso – gonadal axis with possible incapacity to procreate, but that does not seem to be the case, based on our report.

Several organs in addition to the brain express the MAO-B, notably blood, kidneys and liver20, representing sites where MPP+ could be generated. However, the dopamine transporter may not be present within the testis, which is why MPP+ may not have led to a loss of reproductive function. Recently, it was shown that the dopamine transporter may be present on spermatozoids21, suggesting that perhaps MPTP could be toxic to spermatozoids acutely, but with on-going spermatogenesis, this effect might be short-lived.

MPTP could also be toxic to the autonomic nervous system in rhesus macaques, but a recovery process seems to happen22.

In summary, this report suggests that MPTP administration may not affect the reproductive function in marmosets or, if it does, it is for a limited period of time. Future reports and studies are required to confirm our observations.

Data availability

Underlying data

All data underlying the results are available as part of the article and no additional source data are required.

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Nuara SG, Burgess LA, Hamadjida A et al. The neuro-toxin MPTP does not prevent reproduction in marmosets [version 2; peer review: 2 approved] MNI Open Res 2019, 3:2 (https://doi.org/10.12688/mniopenres.12818.2)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
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Open Peer Review

Current Reviewer Status: ?
Key to Reviewer Statuses VIEW
ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions
Version 2
VERSION 2
PUBLISHED 22 May 2019
Revised
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Reviewer Report 04 Jun 2019
Cécile Moro, CEA, LETI, CLINATEC, University of Grenoble Alpes, Grenoble, France 
Approved
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I confirm that I have read this submission and believe that I have an ... Continue reading
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Moro C. Reviewer Report For: The neuro-toxin MPTP does not prevent reproduction in marmosets [version 2; peer review: 2 approved]. MNI Open Res 2019, 3:2 (https://doi.org/10.21956/mniopenres.13885.r26171)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
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Reviewer Report 22 May 2019
Joachim Wistuba, Centre of Reproductive Medicine and Andrology, Institute of Reproductive and Regenerative Biology, Münster, Germany 
Approved
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All my comments ... Continue reading
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CITE
HOW TO CITE THIS REPORT
Wistuba J. Reviewer Report For: The neuro-toxin MPTP does not prevent reproduction in marmosets [version 2; peer review: 2 approved]. MNI Open Res 2019, 3:2 (https://doi.org/10.21956/mniopenres.13885.r26172)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
Version 1
VERSION 1
PUBLISHED 26 Apr 2019
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Reviewer Report 16 May 2019
Cécile Moro, CEA, LETI, CLINATEC, University of Grenoble Alpes, Grenoble, France 
Approved with Reservations
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Nuara et al provide a report on marmouset reproduction after MPTP toxin exposure. This case report is interesting as very few is known about it on literature. However, it is more a case report than an experimental plan to study ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Moro C. Reviewer Report For: The neuro-toxin MPTP does not prevent reproduction in marmosets [version 2; peer review: 2 approved]. MNI Open Res 2019, 3:2 (https://doi.org/10.21956/mniopenres.13882.r26170)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 22 May 2019
    Philippe Huot, Montreal Neurological Institute and Hospital, Montreal, Canada
    22 May 2019
    Author Response
    However, it is more a case report than an experimental plan to study effets of MPTP on reproduction.
    This is a concern we have had from the moment we began ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 22 May 2019
    Philippe Huot, Montreal Neurological Institute and Hospital, Montreal, Canada
    22 May 2019
    Author Response
    However, it is more a case report than an experimental plan to study effets of MPTP on reproduction.
    This is a concern we have had from the moment we began ... Continue reading
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Cite
Reviewer Report 13 May 2019
Joachim Wistuba, Centre of Reproductive Medicine and Andrology, Institute of Reproductive and Regenerative Biology, Münster, Germany 
Approved
VIEWS 0
In their report the authors conclude that MPTP, a neuro-toxin used to induce a Parkinson’s disease like phenotype in non-human primates has no or only limited effect on reproductive ability in marmoset monkeys. They observed a male marmoset which was ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Wistuba J. Reviewer Report For: The neuro-toxin MPTP does not prevent reproduction in marmosets [version 2; peer review: 2 approved]. MNI Open Res 2019, 3:2 (https://doi.org/10.21956/mniopenres.13882.r26166)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 22 May 2019
    Philippe Huot, Montreal Neurological Institute and Hospital, Montreal, Canada
    22 May 2019
    Author Response
    In case of the pair the female was treated with contraception it was not clear to me why she got pregnant at all? In line with this it might be ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 22 May 2019
    Philippe Huot, Montreal Neurological Institute and Hospital, Montreal, Canada
    22 May 2019
    Author Response
    In case of the pair the female was treated with contraception it was not clear to me why she got pregnant at all? In line with this it might be ... Continue reading
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
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